Item | Value |
---|---|
geneid | 9855 |
ensemblid | ENSG00000006607.14 |
hgncid | 16460 |
symbol | FARP2 |
name | FERM, ARH/RhoGEF and pleckstrin domain protein 2 |
refseq_nuc | NM_014808.4 |
refseq_prot | NP_055623.1 |
ensembl_nuc | ENST00000264042.8 |
ensembl_prot | ENSP00000264042.3 |
mane_status | MANE Select |
chr | chr2 |
start | 241356285 |
end | 241494841 |
strand | + |
ver | v1.2 |
region | chr2:241356285-241494841 |
region5000 | chr2:241351285-241499841 |
regionname0 | FARP2_chr2_241356285_241494841 |
regionname5000 | FARP2_chr2_241351285_241499841 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1054 | 273 | 49 | 44 | 135 | 8 | 35 | 98 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0002 | 0/0 | 1054 | 34 | 0 | 13 | 21 | 0 | 0 | 18 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0003 | 0/0 | 1054 | 28 | 10 | 5 | 6 | 1 | 6 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0004 | 0/0 | 1054 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0005 | 0/0 | 1054 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0006 | 0/0 | 1054 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0007 | 0/0 | 1054 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0008 | 0/0 | 1054 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0009 | 0/0 | 1054 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0010 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0011 | 0/0 | 1054 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0012 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0013 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0014 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0015 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0016 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0017 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0018 | 0/0 | 1054 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0019 | 0/0 | 1054 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
a0020 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | MGEIE others(1049): Show |
chr2 | 241351285 | 241499841 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3162 | 186 | 28 | 24 | 104 | 4 | 25 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0003 | 0/0 | 3162 | 34 | 3 | 5 | 21 | 1 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0004 | 0/0 | 3162 | 30 | 14 | 11 | 0 | 3 | 2 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0006 | 0/0 | 3162 | 13 | 0 | 1 | 8 | 0 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0010 | 0/0 | 3162 | 3 | 0 | 3 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0011 | 0/0 | 3162 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0015 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0019 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0022 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0025 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0001c0032 | 0/1 | 3162 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0002c0002 | 0/0 | 3162 | 34 | 0 | 13 | 21 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0003c0005 | 0/0 | 3162 | 28 | 10 | 5 | 6 | 1 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0004c0007 | 0/0 | 3162 | 11 | 9 | 2 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0005c0008 | 0/0 | 3162 | 8 | 8 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0005c0014 | 0/0 | 3162 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0006c0009 | 0/0 | 3162 | 5 | 0 | 5 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0007c0021 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0007c0028 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0008c0013 | 0/0 | 3162 | 2 | 1 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0009c0012 | 0/0 | 3162 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0010c0020 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0011c0017 | 0/0 | 3162 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0012c0030 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0013c0031 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0014c0029 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0015c0023 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0016c0027 | 0/0 | 3162 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0017c0026 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0018c0018 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0019c0024 | 0/0 | 3162 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 | ||
a0020c0016 | 0/0 | 3162 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ATGGG others(3157): Show |
chr2 | 241351285 | 241499841 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4009 | 179 | 23 | 22 | 104 | 4 | 25 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0001t0002 | 0/0 | 4009 | 4 | 3 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0001t0004 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | ACTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0001t0005 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0001t0009 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0003t0001 | 0/0 | 4009 | 32 | 3 | 4 | 20 | 1 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0003t0007 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0003t0008 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0004t0001 | 0/0 | 4009 | 30 | 14 | 11 | 0 | 3 | 2 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0006t0001 | 0/0 | 4009 | 13 | 0 | 1 | 8 | 0 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0010t0001 | 0/0 | 4009 | 3 | 0 | 3 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0011t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0015t0002 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0019t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0022t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0025t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0001c0032t0001 | 0/1 | 4009 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0002c0002t0001 | 0/0 | 4009 | 33 | 0 | 13 | 20 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0002c0002t0006 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0003c0005t0001 | 0/0 | 4009 | 27 | 10 | 4 | 6 | 1 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0003c0005t0003 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0004c0007t0001 | 0/0 | 4009 | 11 | 9 | 2 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0005c0008t0001 | 0/0 | 4009 | 8 | 8 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0005c0014t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0006c0009t0001 | 0/0 | 4009 | 5 | 0 | 5 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0007c0021t0003 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0007c0028t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0008c0013t0001 | 0/0 | 4009 | 2 | 1 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0009c0012t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0010c0020t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0011c0017t0001 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0012c0030t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0013c0031t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0014c0029t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0015c0023t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0016c0027t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0017c0026t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0018c0018t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0019c0024t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
a0020c0016t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | AGTTG others(4004): Show |
chr2 | 241351285 | 241499841 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0003t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0004t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0010t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0010t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0010t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0011t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0011t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0015t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0019t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0022t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0025t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0001c0032t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0002c0002t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0003c0005t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0004c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0008t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0014t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0005c0014t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0006c0009t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0006c0009t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0006c0009t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0006c0009t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0006c0009t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0007c0021t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0007c0028t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0008c0013t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0008c0013t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0009c0012t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0009c0012t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0010c0020t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0011c0017t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0012c0030t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0013c0031t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0014c0029t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0015c0023t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0016c0027t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0017c0026t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0018c0018t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0019c0024t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
a0020c0016t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0005 | t0001 | g0039 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0170 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0172 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00140 | hp2 | a0007 | c0021 | t0003 | g0334 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00323 | hp1 | a0010 | c0020 | t0001 | g0155 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00408 | hp1 | a0001 | c0006 | t0001 | g0244 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00597 | hp2 | a0001 | c0006 | t0001 | g0245 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00621 | hp2 | a0001 | c0006 | t0001 | g0242 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0173 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0348 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG00741 | hp2 | a0001 | c0010 | t0001 | g0364 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01069 | hp2 | a0001 | c0010 | t0001 | g0363 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0178 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0181 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01071 | hp2 | a0001 | c0010 | t0001 | g0365 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01074 | hp1 | a0001 | c0004 | t0001 | g0174 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0344 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01081 | hp2 | a0006 | c0009 | t0001 | g0187 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01099 | hp1 | a0004 | c0007 | t0001 | g0105 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01106 | hp1 | a0001 | c0003 | t0008 | g0061 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01109 | hp1 | a0004 | c0007 | t0001 | g0130 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0165 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01168 | hp2 | a0006 | c0009 | t0001 | g0183 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01169 | hp1 | a0006 | c0009 | t0001 | g0184 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0180 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0357 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01192 | hp2 | a0001 | c0006 | t0001 | g0243 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01243 | hp1 | a0001 | c0004 | t0001 | g0177 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0349 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0171 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01261 | hp1 | a0006 | c0009 | t0001 | g0185 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0372 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0182 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0347 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0179 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01496 | hp2 | a0003 | c0005 | t0001 | g0190 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | IBS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01884 | hp1 | a0003 | c0005 | t0001 | g0199 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01928 | hp1 | a0003 | c0005 | t0001 | g0010 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01934 | hp2 | a0003 | c0005 | t0001 | g0194 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0350 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01981 | hp1 | a0011 | c0017 | t0001 | g0255 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0352 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0351 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02004 | hp2 | a0003 | c0005 | t0003 | g0058 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02055 | hp1 | a0007 | c0028 | t0001 | g0018 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02055 | hp2 | a0003 | c0005 | t0001 | g0045 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02056 | hp1 | a0001 | c0006 | t0001 | g0241 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02071 | hp2 | a0001 | c0006 | t0001 | g0240 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02145 | hp2 | a0008 | c0013 | t0001 | g0191 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02155 | hp1 | a0001 | c0022 | t0001 | g0129 | EAS | CDX | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CDX | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0359 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0378 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02258 | hp2 | a0004 | c0007 | t0001 | g0156 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0345 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02451 | hp1 | a0003 | c0005 | t0001 | g0196 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02451 | hp2 | a0005 | c0008 | t0001 | g0147 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0164 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0375 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02615 | hp1 | a0005 | c0008 | t0001 | g0154 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02622 | hp1 | a0003 | c0005 | t0001 | g0198 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02630 | hp1 | a0005 | c0008 | t0001 | g0153 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02630 | hp2 | a0009 | c0012 | t0001 | g0002 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02647 | hp1 | a0005 | c0008 | t0001 | g0149 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0021 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02698 | hp2 | a0001 | c0006 | t0001 | g0246 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02717 | hp1 | a0004 | c0007 | t0001 | g0096 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02735 | hp1 | a0013 | c0031 | t0001 | g0019 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0373 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02818 | hp1 | a0001 | c0011 | t0001 | g0107 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02818 | hp2 | a0009 | c0012 | t0001 | g0001 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02886 | hp1 | a0001 | c0011 | t0001 | g0108 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02886 | hp2 | a0004 | c0007 | t0001 | g0114 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02895 | hp2 | a0004 | c0007 | t0001 | g0101 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0175 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02897 | hp2 | a0004 | c0007 | t0001 | g0102 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02965 | hp1 | a0014 | c0029 | t0001 | g0030 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02965 | hp2 | a0015 | c0023 | t0001 | g0203 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02970 | hp2 | a0005 | c0008 | t0001 | g0148 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0370 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0167 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03098 | hp2 | a0004 | c0007 | t0001 | g0097 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03130 | hp1 | a0003 | c0005 | t0001 | g0193 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03130 | hp2 | a0001 | c0001 | t0009 | g0106 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03139 | hp1 | a0005 | c0008 | t0001 | g0146 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03139 | hp2 | a0001 | c0025 | t0001 | g0160 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03195 | hp1 | a0004 | c0007 | t0001 | g0121 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03195 | hp2 | a0003 | c0005 | t0001 | g0197 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0159 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03239 | hp2 | a0003 | c0005 | t0001 | g0050 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03486 | hp1 | a0005 | c0014 | t0001 | g0150 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03486 | hp2 | a0004 | c0007 | t0001 | g0100 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03490 | hp1 | a0003 | c0005 | t0001 | g0041 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03492 | hp1 | a0003 | c0005 | t0001 | g0040 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0369 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03540 | hp1 | a0001 | c0004 | t0001 | g0362 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03540 | hp2 | a0016 | c0027 | t0001 | g0145 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03579 | hp1 | a0005 | c0008 | t0001 | g0144 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03688 | hp2 | a0003 | c0005 | t0001 | g0059 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03831 | hp2 | a0001 | c0006 | t0001 | g0251 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03834 | hp1 | a0003 | c0005 | t0001 | g0052 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03927 | hp1 | a0017 | c0026 | t0001 | g0118 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03942 | hp1 | a0001 | c0006 | t0001 | g0249 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04184 | hp2 | a0003 | c0005 | t0001 | g0049 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04199 | hp1 | a0001 | c0004 | t0001 | g0176 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04204 | hp1 | a0001 | c0006 | t0001 | g0250 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18522 | hp2 | a0003 | c0005 | t0001 | g0195 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0360 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18906 | hp2 | a0001 | c0015 | t0002 | g0371 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18945 | hp2 | a0001 | c0019 | t0001 | g0111 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18951 | hp2 | a0002 | c0002 | t0006 | g0252 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18953 | hp2 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18963 | hp2 | a0003 | c0005 | t0001 | g0044 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18964 | hp2 | a0003 | c0005 | t0001 | g0051 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18970 | hp2 | a0018 | c0018 | t0001 | g0338 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18972 | hp1 | a0001 | c0003 | t0007 | g0037 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18984 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18988 | hp1 | a0019 | c0024 | t0001 | g0087 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18998 | hp2 | a0003 | c0005 | t0001 | g0047 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19002 | hp2 | a0003 | c0005 | t0001 | g0042 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0361 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19043 | hp2 | a0004 | c0007 | t0001 | g0115 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19074 | hp1 | a0003 | c0005 | t0001 | g0046 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19077 | hp1 | a0001 | c0006 | t0001 | g0247 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19085 | hp2 | a0001 | c0006 | t0001 | g0248 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19240 | hp1 | a0003 | c0005 | t0001 | g0192 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ASW | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0166 | EUR | TSI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20805 | hp2 | a0020 | c0016 | t0001 | g0321 | EUR | TSI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20905 | hp1 | a0008 | c0013 | t0001 | g0029 | SAS | GIH | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01123 | hp1 | a0003 | c0005 | t0001 | g0057 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG01123 | hp2 | a0006 | c0009 | t0001 | g0186 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02486 | hp1 | a0012 | c0030 | t0001 | g0006 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0374 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0162 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG06807 | hp1 | a0005 | c0008 | t0001 | g0151 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20300 | hp1 | a0005 | c0014 | t0001 | g0152 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
NA21309 | hp2 | a0003 | c0005 | t0001 | g0048 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
homoSapiens | chm13v2 | a0001 | c0032 | t0001 | g0227 | REF | REF | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0099 | REF | REF | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241373157 | G | A | 1 | a0006 | 5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
missense_variant | MODERATE | c.50G>A | p.Arg17His | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/27 | 178/4009 | 50/3165 | 17/1054 | chr2 | 241373157 | |||
chr2:241373241 | A | G | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.134A>G | p.His45Arg | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/27 | 262/4009 | 134/3165 | 45/1054 | chr2 | 241373241 | |||
chr2:241413353 | A | C | 2 | a0005 a0016 |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
missense_variant | MODERATE | c.555A>C | p.Lys185Asn | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/27 | 683/4009 | 555/3165 | 185/1054 | chr2 | 241413353 | |||
chr2:241431686 | C | T | 2 | a0003 a0008 |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
missense_variant | MODERATE | c.779C>T | p.Thr260Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/27 | 907/4009 | 779/3165 | 260/1054 | chr2 | 241431686 | |||
chr2:241441319 | G | A | 1 | a0020 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1174G>A | p.Glu392Lys | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1302/4009 | 1174/3165 | 392/1054 | chr2 | 241441319 | |||
chr2:241456756 | C | T | 1 | a0017 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1421C>T | p.Thr474Met | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/27 | 1549/4009 | 1421/3165 | 474/1054 | chr2 | 241456756 | |||
chr2:241462601 | G | A | 1 | a0010 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1666G>A | p.Val556Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/27 | 1794/4009 | 1666/3165 | 556/1054 | chr2 | 241462601 | |||
chr2:241468173 | G | A | 3 | a0003 a0007 a0016 |
31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
missense_variant | MODERATE | c.1927G>A | p.Val643Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2055/4009 | 1927/3165 | 643/1054 | chr2 | 241468173 | |||
chr2:241468312 | G | A | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2066G>A | p.Arg689His | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2194/4009 | 2066/3165 | 689/1054 | chr2 | 241468312 | |||
chr2:241468326 | C | T | 1 | a0019 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.2080C>T | p.Arg694Cys | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2208/4009 | 2080/3165 | 694/1054 | chr2 | 241468326 | |||
chr2:241475910 | C | T | 1 | a0004 | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
missense_variant | MODERATE | c.2185C>T | p.Arg729Trp | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/27 | 2313/4009 | 2185/3165 | 729/1054 | chr2 | 241475910 | |||
chr2:241475962 | T | C | 1 | a0011 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.2237T>C | p.Ile746Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/27 | 2365/4009 | 2237/3165 | 746/1054 | chr2 | 241475962 | |||
chr2:241490013 | G | A | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2473G>A | p.Ala825Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/27 | 2601/4009 | 2473/3165 | 825/1054 | chr2 | 241490013 | |||
chr2:241491065 | C | T | 1 | a0012 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2509C>T | p.Arg837Trp | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/27 | 2637/4009 | 2509/3165 | 837/1054 | chr2 | 241491065 | |||
chr2:241491173 | C | T | 1 | a0009 | 2 | HG02630.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.2617C>T | p.Pro873Ser | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/27 | 2745/4009 | 2617/3165 | 873/1054 | chr2 | 241491173 | |||
chr2:241491579 | C | T | 3 | a0002 a0011 a0018 |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
missense_variant | MODERATE | c.2687C>T | p.Ser896Phe | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/27 | 2815/4009 | 2687/3165 | 896/1054 | chr2 | 241491579 | |||
chr2:241491618 | T | C | 1 | a0018 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2726T>C | p.Met909Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/27 | 2854/4009 | 2726/3165 | 909/1054 | chr2 | 241491618 | |||
chr2:241493404 | G | A | 1 | a0014 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3007G>A | p.Val1003Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/27 | 3135/4009 | 3007/3165 | 1003/1054 | chr2 | 241493404 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241411051 | A | G | 5 | a0001c0003 a0007c0028 a0012c0030 others(2): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
synonymous_variant | LOW | c.429A>G | p.Gln143Gln | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/27 | 557/4009 | 429/3165 | 143/1054 | chr2 | 241411051 | |||
chr2:241413332 | G | A | 1 | a0001c0011 | 2 | HG02818.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.534G>A | p.Thr178Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/27 | 662/4009 | 534/3165 | 178/1054 | chr2 | 241413332 | |||
chr2:241436502 | G | A | 1 | a0001c0015 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1122G>A | p.Thr374Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/27 | 1250/4009 | 1122/3165 | 374/1054 | chr2 | 241436502 | |||
chr2:241441333 | T | A | 4 | a0001c0006 a0002c0002 a0011c0017 others(1): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
synonymous_variant | LOW | c.1188T>A | p.Thr396Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1316/4009 | 1188/3165 | 396/1054 | chr2 | 241441333 | |||
chr2:241441516 | G | A | 1 | a0001c0019 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.1371G>A | p.Ser457Ser | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1499/4009 | 1371/3165 | 457/1054 | chr2 | 241441516 | |||
chr2:241462609 | C | T | 2 | a0001c0025 a0005c0008 |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
synonymous_variant | LOW | c.1674C>T | p.Thr558Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/27 | 1802/4009 | 1674/3165 | 558/1054 | chr2 | 241462609 | |||
chr2:241463391 | G | C | 1 | a0001c0010 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.1734G>C | p.Leu578Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/27 | 1862/4009 | 1734/3165 | 578/1054 | chr2 | 241463391 | |||
chr2:241468244 | G | A | 1 | a0001c0022 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1998G>A | p.Leu666Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2126/4009 | 1998/3165 | 666/1054 | chr2 | 241468244 | |||
chr2:241468331 | A | G | 2 | a0001c0004 a0001c0010 |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.2085A>G | p.Leu695Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2213/4009 | 2085/3165 | 695/1054 | chr2 | 241468331 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241356286 | G | C | 1 | a0001c0001t0004 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/27 | 16822 | chr2 | 241356286 | ||||||
chr2:241356355 | G | A | 2 | a0001c0001t0002 a0001c0015t0002 |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-58G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/27 | 16753 | chr2 | 241356355 | ||||||
chr2:241494371 | G | A | 1 | a0001c0001t0005 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 246 | chr2 | 241494371 | ||||||
chr2:241494492 | G | A | 1 | a0002c0002t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 367 | chr2 | 241494492 | ||||||
chr2:241494538 | C | T | 2 | a0003c0005t0003 a0007c0021t0003 |
2 | HG00140.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*413C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 413 | chr2 | 241494538 | ||||||
chr2:241494575 | G | A | 1 | a0001c0003t0007 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 450 | chr2 | 241494575 | ||||||
chr2:241494613 | G | A | 1 | a0001c0003t0008 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 488 | chr2 | 241494613 | ||||||
chr2:241494660 | G | T | 1 | a0001c0001t0009 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 535 | chr2 | 241494660 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241356420 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+32G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356420 | |||||||
chr2:241356514 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-25+126T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356514 | |||||||
chr2:241356799 | A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+411A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356799 | |||||||
chr2:241356816 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-25+428C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356816 | |||||||
chr2:241356845 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+457G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356845 | |||||||
chr2:241356858 | G | C | 57 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.-25+470G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356858 | |||||||
chr2:241356863 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-25+475G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356863 | |||||||
chr2:241357015 | C | G | 2 | a0001c0001t0001g0376 a0001c0001t0001g0377 |
2 | NA18968.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-25+627C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357015 | |||||||
chr2:241357034 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(188): Show |
191 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-25+646A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357034 | |||||||
chr2:241357154 | A | T | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-25+766A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357154 | |||||||
chr2:241357221 | C | A | 10 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(7): Show |
10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+833C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357221 | |||||||
chr2:241357313 | G | A | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-25+925G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357313 | |||||||
chr2:241357341 | ACAG | A | 9 | a0001c0001t0001g0378 a0001c0001t0002g0372 a0001c0001t0002g0373 others(6): Show |
9 | HG01261.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+954_-25+956del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357341 | |||||||
chr2:241357402 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG00558.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-25+1014C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357402 | |||||||
chr2:241357425 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-25+1037G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357425 | |||||||
chr2:241357676 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-25+1288C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357676 | |||||||
chr2:241357703 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(177): Show |
180 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-25+1315G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357703 | |||||||
chr2:241357757 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+1369C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357757 | |||||||
chr2:241357776 | C | T | 2 | a0003c0005t0001g0198 a0003c0005t0001g0199 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-25+1388C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357776 | |||||||
chr2:241357843 | A | G | 1 | a0004c0007t0001g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-25+1455A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357843 | |||||||
chr2:241357925 | A | G | 2 | a0001c0003t0001g0060 a0001c0003t0008g0061 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-25+1537A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357925 | |||||||
chr2:241357984 | G | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-25+1596G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357984 | |||||||
chr2:241358186 | C | T | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-25+1798C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358186 | |||||||
chr2:241358203 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1815A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358203 | |||||||
chr2:241358209 | A | T | 2 | a0003c0005t0001g0057 a0003c0005t0003g0058 |
2 | HG01123.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-25+1821A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358209 | |||||||
chr2:241358426 | A | G | 5 | a0006c0009t0001g0183 a0006c0009t0001g0184 a0006c0009t0001g0185 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+2038A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358426 | |||||||
chr2:241358648 | G | A | 1 | a0002c0002t0001g0200 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-25+2260G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358648 | |||||||
chr2:241358696 | C | T | 6 | a0001c0004t0001g0177 a0001c0004t0001g0178 a0001c0004t0001g0179 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2308C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358696 | |||||||
chr2:241358748 | G | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+2360G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358748 | |||||||
chr2:241358813 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+2425G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358813 | |||||||
chr2:241358866 | C | T | 26 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-25+2478C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358866 | |||||||
chr2:241358920 | T | C | 3 | a0001c0001t0001g0378 a0009c0012t0001g0001 a0009c0012t0001g0002 |
3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+2532T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358920 | |||||||
chr2:241359078 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-25+2690T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359078 | |||||||
chr2:241359293 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-25+2905A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359293 | |||||||
chr2:241359338 | C | G | 1 | a0006c0009t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+2950C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359338 | |||||||
chr2:241359421 | T | C | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-25+3033T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359421 | |||||||
chr2:241359453 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0378 |
3 | HG02257.hp1 HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+3065G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359453 | |||||||
chr2:241359517 | C | G | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-25+3129C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359517 | |||||||
chr2:241359786 | T | G | 1 | a0003c0005t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-25+3398T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359786 | |||||||
chr2:241360141 | A | G | 3 | a0001c0010t0001g0363 a0001c0010t0001g0364 a0001c0010t0001g0365 |
3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-25+3753A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360141 | |||||||
chr2:241360164 | G | T | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-25+3776G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360164 | |||||||
chr2:241360254 | G | A | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-25+3866G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360254 | |||||||
chr2:241360368 | C | T | 8 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(5): Show |
8 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+3980C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360368 | |||||||
chr2:241360660 | C | G | 4 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+4272C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360660 | |||||||
chr2:241360661 | G | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+4273G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360661 | |||||||
chr2:241360668 | T | C | 4 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+4280T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360668 | |||||||
chr2:241360673 | C | CA | 137 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(134): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-25+4302dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241360673 | ||||||
chr2:241360673 | C | CAA | 11 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0366 others(8): Show |
11 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+4301_-25+4302d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241360673 | ||||||
chr2:241360804 | C | A | 11 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(8): Show |
11 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+4416C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360804 | |||||||
chr2:241361028 | G | GA | 34 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-25+4654dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241361028 | ||||||
chr2:241361028 | GA | G | 36 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0004t0001g0143 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-25+4654delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241361028 | ||||||
chr2:241361041 | A | AC | 25 | a0002c0002t0001g0200 a0002c0002t0001g0335 a0002c0002t0001g0336 others(22): Show |
25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25+4653_-25+4654i others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361041 | |||||||
chr2:241361041 | A | C | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+4653A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361041 | |||||||
chr2:241361044 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-25+4656A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361044 | |||||||
chr2:241361075 | A | G | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-25+4687A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361075 | |||||||
chr2:241361091 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4703T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361091 | |||||||
chr2:241361092 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4704G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361092 | |||||||
chr2:241361093 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4705G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361093 | |||||||
chr2:241361135 | A | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+4747A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361135 | |||||||
chr2:241361191 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-25+4803C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361191 | |||||||
chr2:241361236 | A | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-25+4848A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361236 | |||||||
chr2:241361622 | C | T | 1 | a0007c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+5234C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361622 | |||||||
chr2:241361675 | T | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+5287T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361675 | |||||||
chr2:241361682 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-25+5294A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361682 | |||||||
chr2:241361948 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-25+5560G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361948 | |||||||
chr2:241361998 | G | A | 2 | a0006c0009t0001g0183 a0006c0009t0001g0184 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-25+5610G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361998 | |||||||
chr2:241362429 | C | T | 10 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(7): Show |
10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+6041C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362429 | |||||||
chr2:241362471 | G | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-25+6083G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362471 | |||||||
chr2:241362494 | C | T | 1 | a0001c0004t0001g0176 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-25+6106C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362494 | |||||||
chr2:241362552 | A | G | 25 | a0002c0002t0001g0200 a0002c0002t0001g0335 a0002c0002t0001g0336 others(22): Show |
25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25+6164A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362552 | |||||||
chr2:241362567 | T | C | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+6179T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362567 | |||||||
chr2:241362767 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-25+6379G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362767 | |||||||
chr2:241363118 | C | T | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+6730C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363118 | |||||||
chr2:241363396 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-25+7008A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363396 | |||||||
chr2:241363414 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-25+7026C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363414 | |||||||
chr2:241363416 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-25+7028G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363416 | |||||||
chr2:241363430 | G | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+7042G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363430 | |||||||
chr2:241363444 | G | A | 4 | a0001c0006t0001g0240 a0001c0006t0001g0241 a0001c0006t0001g0242 others(1): Show |
4 | HG00621.hp2 HG01192.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+7056G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363444 | |||||||
chr2:241363519 | T | C | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+7131T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363519 | |||||||
chr2:241363679 | C | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-25+7291C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363679 | |||||||
chr2:241363943 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-25+7555G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363943 | |||||||
chr2:241364041 | T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-25+7653T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364041 | |||||||
chr2:241364076 | C | T | 3 | a0001c0001t0001g0378 a0009c0012t0001g0001 a0009c0012t0001g0002 |
3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+7688C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364076 | |||||||
chr2:241364302 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-25+7914G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364302 | |||||||
chr2:241364558 | A | C | 3 | a0001c0001t0001g0235 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | NA18943.hp2 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-25+8170A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364558 | |||||||
chr2:241364792 | G | A | 16 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(13): Show |
16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24-8292G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364792 | |||||||
chr2:241364927 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24-8157C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364927 | |||||||
chr2:241364940 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-8144G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364940 | |||||||
chr2:241365282 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-24-7802C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365282 | |||||||
chr2:241365376 | G | A | 48 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-7708G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365376 | |||||||
chr2:241365695 | G | A | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7389G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365695 | |||||||
chr2:241365697 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-24-7387A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365697 | |||||||
chr2:241365742 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24-7342T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365742 | |||||||
chr2:241365765 | A | G | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-24-7319A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365765 | |||||||
chr2:241365790 | C | A | 48 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-7294C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365790 | |||||||
chr2:241365974 | C | CT | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-7097dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241365974 | ||||||
chr2:241366092 | TA | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(23): Show |
26 | HG00544.hp2 HG00639.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-24-6979delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366092 | ||||||
chr2:241366100 | A | AATAT | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-24-6983_-24-6982i others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366100 | ||||||
chr2:241366100 | A | T | 24 | a0003c0005t0001g0039 a0003c0005t0001g0040 a0003c0005t0001g0041 others(21): Show |
24 | HG00099.hp1 HG02055.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-6984A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366100 | |||||||
chr2:241366102 | A | AAT | 8 | a0003c0005t0001g0190 a0003c0005t0001g0195 a0003c0005t0001g0196 others(5): Show |
8 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24-6981_-24-6980i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366102 | ||||||
chr2:241366102 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-24-6981_-24-6980i others(30): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366102 | ||||||
chr2:241366102 | A | T | 117 | a0001c0003t0001g0007 a0001c0003t0001g0011 a0001c0003t0001g0012 others(114): Show |
117 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-24-6982A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366102 | |||||||
chr2:241366104 | A | AAATATAT others(2): Show |
11 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(8): Show |
11 | HG01934.hp1 HG02071.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-6979_-24-6978i others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366104 | ||||||
chr2:241366104 | A | AAATATAT others(4): Show |
15 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0074 others(12): Show |
15 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24-6979_-24-6978i others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366104 | ||||||
chr2:241366104 | A | C | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-24-6980A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366104 | |||||||
chr2:241366104 | A | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0135 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-24-6980A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366104 | |||||||
chr2:241366106 | T | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0141 a0004c0007t0001g0096 others(1): Show |
4 | HG01099.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6978T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366106 | |||||||
chr2:241366106 | T | TATATATA others(19): Show |
24 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(21): Show |
24 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366106 | ||||||
chr2:241366108 | T | TATATATA others(17): Show |
2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366108 | ||||||
chr2:241366108 | T | TATATATA others(45): Show |
1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-24-6965_-24-6964i others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366108 | ||||||
chr2:241366109 | A | ATATATAT others(5): Show |
1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-24-6967_-24-6966i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366109 | ||||||
chr2:241366110 | T | TATATATA others(3): Show |
65 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 others(62): Show |
65 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366110 | ||||||
chr2:241366111 | A | ATATATAT others(53): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0188 a0004c0007t0001g0100 others(2): Show |
5 | HG00558.hp1 HG02145.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | ||||||
chr2:241366111 | A | ATATATAT others(55): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0093 others(36): Show |
39 | HG00544.hp1 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | ||||||
chr2:241366111 | A | ATATATAT others(53): Show |
1 | a0010c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-24-6963_-24-6962i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | ||||||
chr2:241366111 | A | ATATATAT others(57): Show |
2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(66): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | ||||||
chr2:241366111 | A | ATATATAT others(57): Show |
5 | a0001c0001t0001g0095 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG01099.hp2 HG02083.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(66): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | ||||||
chr2:241366120 | T | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6964T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366120 | |||||||
chr2:241366122 | C | T | 85 | a0001c0001t0001g0088 a0001c0001t0001g0136 a0001c0001t0001g0158 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.-24-6962C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366122 | |||||||
chr2:241366123 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0136 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.-24-6961G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366123 | |||||||
chr2:241366123 | GTA | G | 27 | a0001c0001t0001g0228 a0001c0001t0001g0304 a0001c0001t0001g0305 others(24): Show |
27 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-24-6946_-24-6945d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366123 | ||||||
chr2:241366124 | T | TATATATA others(5): Show |
1 | a0001c0006t0001g0246 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366124 | ||||||
chr2:241366125 | A | ACACGTAT others(25): Show |
1 | a0001c0003t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24-6959_-24-6958i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366125 | |||||||
chr2:241366125 | A | ATACACGT others(27): Show |
1 | a0006c0009t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-24-6957_-24-6956i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATACGTAT others(25): Show |
33 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(30): Show |
33 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-24-6957_-24-6956i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACAC others(27): Show |
11 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(8): Show |
11 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACGT others(27): Show |
7 | a0001c0003t0001g0033 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
7 | HG00280.hp1 HG02004.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACGT others(53): Show |
1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACGT others(55): Show |
2 | a0001c0003t0001g0054 a0001c0003t0001g0055 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACGT others(107): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(116): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATACGT others(55): Show |
1 | a0001c0003t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAC others(29): Show |
18 | a0001c0004t0001g0164 a0001c0004t0001g0165 a0001c0004t0001g0166 others(15): Show |
18 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24-6953_-24-6952i others(38): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAC others(29): Show |
1 | a0003c0005t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-24-6953_-24-6952i others(38): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(31): Show |
1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(40): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(17): Show |
5 | a0001c0001t0001g0235 a0001c0001t0001g0328 a0001c0001t0001g0330 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6951_-24-6950i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(3): Show |
4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6951_-24-6950i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(31): Show |
1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(40): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(52): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(19): Show |
69 | a0001c0001t0001g0378 a0001c0001t0002g0372 a0001c0001t0002g0373 others(66): Show |
69 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(45): Show |
2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(71): Show |
21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(80): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(97): Show |
1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(106): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(68): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(73): Show |
3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | NA18982.hp2 NA18995.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(47): Show |
1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(56): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(73): Show |
1 | a0001c0006t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(5): Show |
65 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 others(62): Show |
65 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(83): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(92): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(53): Show |
24 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(21): Show |
24 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366125 | A | ATATATAT others(93): Show |
1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-24-6945_-24-6944i others(102): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | ||||||
chr2:241366127 | A | ACGTATAT others(25): Show |
1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-24-6957_-24-6956i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366127 | |||||||
chr2:241366127 | A | ATATATAT others(17): Show |
9 | a0005c0008t0001g0144 a0005c0008t0001g0148 a0005c0008t0001g0149 others(6): Show |
9 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366127 | ||||||
chr2:241366127 | A | ATATATAT others(3): Show |
1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366127 | ||||||
chr2:241366129 | A | ATATATAC others(15): Show |
1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366129 | ||||||
chr2:241366130 | T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6954T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366130 | |||||||
chr2:241366131 | A | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6953A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366131 | |||||||
chr2:241366133 | A | ATACATAT others(73): Show |
1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366133 | ||||||
chr2:241366138 | T | C | 50 | a0001c0001t0001g0378 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-24-6946T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366138 | |||||||
chr2:241366140 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366140 | |||||||
chr2:241366142 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6942C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366142 | |||||||
chr2:241366146 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6938C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366146 | |||||||
chr2:241366148 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6936C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366148 | |||||||
chr2:241366157 | T | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6927T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366157 | |||||||
chr2:241366158 | TTCTTCCT others(3444): Show |
T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6925_-24-3475d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366158 | |||||||
chr2:241366294 | C | T | 1 | a0003c0005t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-24-6790C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366294 | |||||||
chr2:241366360 | T | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-6724T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366360 | |||||||
chr2:241366440 | A | G | 1 | a0005c0008t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-24-6644A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366440 | |||||||
chr2:241367201 | G | A | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-5883G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241367201 | |||||||
chr2:241367633 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-24-5451G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241367633 | |||||||
chr2:241367875 | C | CT | 14 | a0001c0001t0001g0095 a0001c0001t0001g0103 a0001c0001t0001g0116 others(11): Show |
14 | HG01099.hp2 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-24-5198dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241367875 | ||||||
chr2:241368048 | CATT | C | 35 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(32): Show |
35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-5033_-24-5031d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241368048 | ||||||
chr2:241368188 | G | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-4896G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368188 | |||||||
chr2:241368237 | G | A | 1 | a0003c0005t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-24-4847G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368237 | |||||||
chr2:241368409 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-24-4675G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368409 | |||||||
chr2:241368413 | C | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-24-4671C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368413 | |||||||
chr2:241368547 | C | T | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-4537C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368547 | |||||||
chr2:241368611 | G | A | 1 | a0001c0001t0009g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-4473G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368611 | |||||||
chr2:241368624 | A | T | 287 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-24-4460A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368624 | |||||||
chr2:241368633 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-4451A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368633 | |||||||
chr2:241368700 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-4384A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368700 | |||||||
chr2:241368889 | A | C | 1 | a0001c0003t0001g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-24-4195A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368889 | |||||||
chr2:241369126 | G | A | 1 | a0001c0006t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-24-3958G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369126 | |||||||
chr2:241369202 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24-3882G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369202 | |||||||
chr2:241369210 | GTTTT | G | 5 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0052 others(2): Show |
5 | HG00099.hp1 HG01123.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3871_-24-3868d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241369210 | ||||||
chr2:241369234 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24-3850T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369234 | |||||||
chr2:241369397 | CCTT | C | 35 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(32): Show |
35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-3684_-24-3682d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241369397 | ||||||
chr2:241369571 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-24-3513A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369571 | |||||||
chr2:241369612 | T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3472T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369612 | |||||||
chr2:241369614 | T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3470T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369614 | |||||||
chr2:241369617 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3467A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369617 | |||||||
chr2:241369625 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3459C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369625 | |||||||
chr2:241369626 | T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3458T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369626 | |||||||
chr2:241369629 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3455A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369629 | |||||||
chr2:241369630 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3454G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369630 | |||||||
chr2:241369631 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3453A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369631 | |||||||
chr2:241369633 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3451A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369633 | |||||||
chr2:241369639 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3445A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369639 | |||||||
chr2:241369647 | T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3437T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369647 | |||||||
chr2:241369652 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3432C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369652 | |||||||
chr2:241369654 | G | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3430G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369654 | |||||||
chr2:241369655 | T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3429T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369655 | |||||||
chr2:241369656 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3428A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369656 | |||||||
chr2:241369658 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3426A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369658 | |||||||
chr2:241369662 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3422A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369662 | |||||||
chr2:241369671 | A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3413A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369671 | |||||||
chr2:241369721 | G | A | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-3363G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369721 | |||||||
chr2:241369803 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-24-3281T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369803 | |||||||
chr2:241369841 | T | C | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-24-3243T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369841 | |||||||
chr2:241369998 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-3086A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369998 | |||||||
chr2:241370375 | C | T | 48 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-2709C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370375 | |||||||
chr2:241370703 | A | G | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-24-2381A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370703 | |||||||
chr2:241370759 | T | C | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-24-2325T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370759 | |||||||
chr2:241370846 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-2238A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370846 | |||||||
chr2:241370896 | T | C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | NA18953.hp1 NA19000.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2188T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370896 | |||||||
chr2:241371006 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-24-2078G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371006 | |||||||
chr2:241371011 | G | A | 4 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(1): Show |
4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-2073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371011 | |||||||
chr2:241371040 | G | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-2044G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371040 | |||||||
chr2:241371208 | G | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-1876G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371208 | |||||||
chr2:241371438 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-24-1646G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371438 | |||||||
chr2:241371479 | G | A | 1 | a0001c0004t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-24-1605G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371479 | |||||||
chr2:241371562 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-24-1522C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371562 | |||||||
chr2:241371579 | C | T | 10 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(7): Show |
10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-1505C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371579 | |||||||
chr2:241371713 | G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24-1371G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371713 | |||||||
chr2:241372090 | CAT | C | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-24-992_-24-991del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241372090 | ||||||
chr2:241372094 | G | A | 5 | a0006c0009t0001g0183 a0006c0009t0001g0184 a0006c0009t0001g0185 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-990G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372094 | |||||||
chr2:241372273 | G | T | 3 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-24-811G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372273 | |||||||
chr2:241372430 | C | T | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-24-654C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372430 | |||||||
chr2:241372601 | G | A | 35 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(32): Show |
35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-483G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372601 | |||||||
chr2:241372717 | G | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-24-367G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372717 | |||||||
chr2:241372731 | G | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-353G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372731 | |||||||
chr2:241372937 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-24-147A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372937 | |||||||
chr2:241372938 | C | CT | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-24-143dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241372938 | ||||||
chr2:241372962 | C | T | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-24-122C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372962 | |||||||
chr2:241372995 | C | T | 1 | a0003c0005t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-24-89C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372995 | |||||||
chr2:241373044 | T | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-40T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241373044 | |||||||
chr2:241373052 | C | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-24-32C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241373052 | |||||||
chr2:241373062 | G | GT | 108 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0092 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
splice_region_variant&intron_variant | LOW | c.-24-9dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241373062 | ||||||
chr2:241373506 | G | A | 1 | a0004c0007t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.183+216G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373506 | |||||||
chr2:241373642 | G | A | 1 | a0001c0006t0001g0247 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.183+352G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373642 | |||||||
chr2:241373948 | A | G | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.183+658A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373948 | |||||||
chr2:241374043 | T | C | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.183+753T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374043 | |||||||
chr2:241374229 | C | T | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+939C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374229 | |||||||
chr2:241374714 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+1424T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374714 | |||||||
chr2:241374745 | G | A | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+1455G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374745 | |||||||
chr2:241374814 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+1524T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374814 | |||||||
chr2:241374858 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1568G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374858 | |||||||
chr2:241374971 | G | A | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+1681G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374971 | |||||||
chr2:241375092 | G | A | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.183+1802G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375092 | |||||||
chr2:241375197 | C | T | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+1907C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375197 | |||||||
chr2:241375408 | C | CT | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2128dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241375408 | ||||||
chr2:241375513 | C | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+2223C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375513 | |||||||
chr2:241375608 | A | G | 4 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0004t0001g0171 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2318A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375608 | |||||||
chr2:241375777 | G | T | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+2487G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375777 | |||||||
chr2:241376025 | A | C | 1 | a0003c0005t0001g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.183+2735A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376025 | |||||||
chr2:241376028 | A | G | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+2738A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376028 | |||||||
chr2:241376191 | A | G | 5 | a0001c0004t0001g0361 a0001c0004t0001g0362 a0001c0010t0001g0363 others(2): Show |
5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+2901A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376191 | |||||||
chr2:241376221 | G | A | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+2931G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376221 | |||||||
chr2:241376404 | A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+3114A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376404 | |||||||
chr2:241376499 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.183+3209T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376499 | |||||||
chr2:241376526 | TC | T | 287 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.183+3241delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241376526 | ||||||
chr2:241376617 | G | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+3327G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376617 | |||||||
chr2:241376646 | G | T | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+3356G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376646 | |||||||
chr2:241376659 | C | T | 1 | a0003c0005t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+3369C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376659 | |||||||
chr2:241376672 | C | T | 1 | a0001c0006t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.183+3382C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376672 | |||||||
chr2:241376748 | G | A | 3 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+3458G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376748 | |||||||
chr2:241376787 | G | A | 3 | a0001c0001t0009g0106 a0001c0011t0001g0107 a0001c0011t0001g0108 |
3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.183+3497G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376787 | |||||||
chr2:241376969 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+3679A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376969 | |||||||
chr2:241377097 | C | T | 25 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+3807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377097 | |||||||
chr2:241377194 | G | A | 1 | a0013c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.183+3904G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377194 | |||||||
chr2:241377333 | CT | C | 69 | a0001c0001t0001g0270 a0001c0001t0001g0378 a0001c0003t0001g0007 others(66): Show |
69 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.183+4062delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241377333 | ||||||
chr2:241377333 | CTT | C | 28 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(25): Show |
28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.183+4061_183+4062d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241377333 | ||||||
chr2:241377352 | T | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4062T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377352 | |||||||
chr2:241377379 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.183+4089G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377379 | |||||||
chr2:241377428 | G | A | 25 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+4138G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377428 | |||||||
chr2:241377464 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4174C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377464 | |||||||
chr2:241377498 | C | T | 1 | a0001c0001t0002g0375 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183+4208C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377498 | |||||||
chr2:241377686 | C | A | 1 | a0001c0001t0009g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.183+4396C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377686 | |||||||
chr2:241377813 | G | A | 2 | a0001c0001t0001g0158 a0001c0004t0001g0157 |
2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.183+4523G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377813 | |||||||
chr2:241377830 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4540G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377830 | |||||||
chr2:241377859 | G | C | 2 | a0002c0002t0001g0200 a0002c0002t0001g0358 |
2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.183+4569G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377859 | |||||||
chr2:241377864 | A | G | 1 | a0004c0007t0001g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183+4574A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377864 | |||||||
chr2:241377892 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+4602C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377892 | |||||||
chr2:241378109 | A | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4819A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378109 | |||||||
chr2:241378140 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+4850C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378140 | |||||||
chr2:241378270 | AT | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.183+4992delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378270 | ||||||
chr2:241378299 | C | T | 2 | a0001c0006t0001g0242 a0001c0006t0001g0243 |
2 | HG00621.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.183+5009C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378299 | |||||||
chr2:241378300 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.183+5010G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378300 | |||||||
chr2:241378362 | C | G | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+5072C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378362 | |||||||
chr2:241378416 | A | ATTTTTTT others(2): Show |
84 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(81): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.183+5131_183+5139d others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | ||||||
chr2:241378416 | A | ATTTTTTT others(3): Show |
105 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.183+5130_183+5139d others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | ||||||
chr2:241378416 | A | ATTTTTTT others(4): Show |
84 | a0001c0001t0001g0004 a0001c0001t0001g0234 a0001c0001t0001g0235 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.183+5129_183+5139d others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | ||||||
chr2:241378416 | A | ATTTTTTT others(5): Show |
17 | a0001c0001t0001g0158 a0001c0001t0001g0239 a0001c0001t0001g0298 others(14): Show |
17 | HG01071.hp1 HG01175.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+5128_183+5139d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | ||||||
chr2:241378506 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.183+5216G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378506 | |||||||
chr2:241378537 | T | C | 290 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.183+5247T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378537 | |||||||
chr2:241378558 | G | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+5268G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378558 | |||||||
chr2:241378874 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.183+5584T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378874 | |||||||
chr2:241379043 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+5753G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379043 | |||||||
chr2:241379086 | G | C | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+5796G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379086 | |||||||
chr2:241379168 | C | G | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+5878C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379168 | |||||||
chr2:241379368 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+6078G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379368 | |||||||
chr2:241379395 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.183+6105C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379395 | |||||||
chr2:241379449 | C | G | 1 | a0005c0008t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+6159C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379449 | |||||||
chr2:241379774 | A | G | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.183+6484A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379774 | |||||||
chr2:241380084 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+6794A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380084 | |||||||
chr2:241380360 | G | T | 18 | a0002c0002t0001g0339 a0002c0002t0001g0340 a0002c0002t0001g0341 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+7070G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380360 | |||||||
chr2:241380378 | C | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+7088C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380378 | |||||||
chr2:241380574 | C | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+7284C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380574 | |||||||
chr2:241380600 | C | A | 1 | a0001c0006t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.183+7310C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380600 | |||||||
chr2:241380661 | A | G | 1 | a0001c0022t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.183+7371A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380661 | |||||||
chr2:241380690 | ATATAT | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+7411_183+7415d others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241380690 | ||||||
chr2:241380878 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+7588C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380878 | |||||||
chr2:241380906 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.183+7616G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380906 | |||||||
chr2:241381187 | T | C | 2 | a0001c0003t0001g0060 a0001c0003t0008g0061 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.183+7897T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381187 | |||||||
chr2:241381235 | C | T | 17 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(14): Show |
17 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+7945C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381235 | |||||||
chr2:241381320 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0109 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+8030G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381320 | |||||||
chr2:241381363 | G | C | 1 | a0001c0004t0001g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.183+8073G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381363 | |||||||
chr2:241381404 | G | A | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.183+8114G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381404 | |||||||
chr2:241381607 | T | G | 2 | a0001c0004t0001g0359 a0001c0004t0001g0360 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+8317T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381607 | |||||||
chr2:241381611 | G | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.183+8321G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381611 | |||||||
chr2:241381656 | G | A | 5 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 others(2): Show |
5 | HG03139.hp1 NA18972.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+8366G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381656 | |||||||
chr2:241381658 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.183+8368A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381658 | |||||||
chr2:241381668 | G | A | 369 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.183+8378G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381668 | |||||||
chr2:241381756 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.183+8466T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381756 | |||||||
chr2:241381828 | G | A | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+8538G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381828 | |||||||
chr2:241381943 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+8653C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381943 | |||||||
chr2:241382170 | A | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+8880A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382170 | |||||||
chr2:241382185 | G | A | 4 | a0005c0008t0001g0144 a0005c0008t0001g0148 a0005c0008t0001g0149 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+8895G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382185 | |||||||
chr2:241382288 | A | ATC | 44 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0234 others(41): Show |
44 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.183+9000_183+9001d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382288 | ||||||
chr2:241382290 | C | CAA | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9000_183+9001i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382290 | |||||||
chr2:241382290 | C | CTCT | 3 | a0001c0001t0001g0238 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG03688.hp1 NA18943.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.183+9001_183+9002i others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382290 | ||||||
chr2:241382291 | T | TC | 38 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0232 others(35): Show |
38 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+9001_183+9002i others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382291 | |||||||
chr2:241382292 | A | AT | 67 | a0001c0001t0001g0091 a0001c0001t0001g0103 a0001c0001t0001g0109 others(64): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.183+9022dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382292 | ||||||
chr2:241382292 | A | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG01070.hp2 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+9002A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382292 | |||||||
chr2:241382292 | A | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0202 a0001c0001t0001g0204 others(89): Show |
92 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.183+9002A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382292 | |||||||
chr2:241382349 | C | T | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+9059C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382349 | |||||||
chr2:241382407 | C | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9117C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382407 | |||||||
chr2:241382410 | A | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9120A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382410 | |||||||
chr2:241382475 | G | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9185G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382475 | |||||||
chr2:241382483 | A | G | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9193A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382483 | |||||||
chr2:241382768 | C | T | 52 | a0001c0001t0001g0378 a0001c0006t0001g0236 a0001c0006t0001g0240 others(49): Show |
52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.183+9478C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382768 | |||||||
chr2:241383015 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+9725G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383015 | |||||||
chr2:241383163 | C | T | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.183+9873C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383163 | |||||||
chr2:241383171 | G | A | 30 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.183+9881G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383171 | |||||||
chr2:241383225 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9935C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383225 | |||||||
chr2:241383236 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.183+9946C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383236 | |||||||
chr2:241383252 | A | G | 369 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.183+9962A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383252 | |||||||
chr2:241383258 | C | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+9968C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383258 | |||||||
chr2:241383265 | T | C | 180 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(177): Show |
180 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.183+9975T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383265 | |||||||
chr2:241383337 | A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+10047A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383337 | |||||||
chr2:241383520 | G | A | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+10230G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383520 | |||||||
chr2:241383702 | G | T | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+10412G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383702 | |||||||
chr2:241383813 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.183+10523G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383813 | |||||||
chr2:241383918 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0226 |
2 | HG03654.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.183+10628C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383918 | |||||||
chr2:241383938 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.183+10648G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383938 | |||||||
chr2:241384108 | A | G | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
9 | HG00639.hp2 HG01167.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+10818A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384108 | |||||||
chr2:241384201 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+10911G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384201 | |||||||
chr2:241384222 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+10932A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384222 | |||||||
chr2:241384360 | C | A | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+11070C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384360 | |||||||
chr2:241384363 | G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183+11073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384363 | |||||||
chr2:241384487 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.183+11197G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384487 | |||||||
chr2:241384524 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+11234C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384524 | |||||||
chr2:241384583 | C | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+11293C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384583 | |||||||
chr2:241384931 | A | G | 1 | a0001c0003t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.183+11641A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384931 | |||||||
chr2:241384964 | A | G | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.183+11674A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384964 | |||||||
chr2:241385272 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+11982A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385272 | |||||||
chr2:241385345 | A | C | 85 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.183+12055A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385345 | |||||||
chr2:241385348 | G | A | 85 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(82): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.183+12058G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385348 | |||||||
chr2:241385356 | T | C | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.183+12066T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385356 | |||||||
chr2:241385472 | G | A | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+12182G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385472 | |||||||
chr2:241385669 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.183+12379G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385669 | |||||||
chr2:241385685 | A | G | 1 | a0002c0002t0001g0261 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.183+12395A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385685 | |||||||
chr2:241385772 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+12482T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385772 | |||||||
chr2:241385966 | T | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+12676T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385966 | |||||||
chr2:241386385 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+13095C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386385 | |||||||
chr2:241386408 | A | G | 323 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(320): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.183+13118A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386408 | |||||||
chr2:241386432 | T | C | 3 | a0002c0002t0001g0335 a0002c0002t0001g0336 a0002c0002t0001g0353 |
3 | NA18952.hp2 NA18963.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.183+13142T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386432 | |||||||
chr2:241386497 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0109 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+13207C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386497 | |||||||
chr2:241386560 | G | C | 7 | a0001c0001t0001g0270 a0001c0001t0001g0278 a0001c0001t0001g0280 others(4): Show |
7 | NA18946.hp2 NA18949.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+13270G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386560 | |||||||
chr2:241386565 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.183+13275G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386565 | |||||||
chr2:241386654 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+13364C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386654 | |||||||
chr2:241386908 | A | G | 289 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.183+13618A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386908 | |||||||
chr2:241386935 | A | G | 1 | a0001c0003t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.183+13645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386935 | |||||||
chr2:241387236 | C | T | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.183+13946C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387236 | |||||||
chr2:241387373 | T | A | 1 | a0003c0005t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+14083T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387373 | |||||||
chr2:241387454 | C | T | 323 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(320): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.183+14164C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387454 | |||||||
chr2:241387532 | G | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG00621.hp1 HG02273.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.183+14242G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387532 | |||||||
chr2:241387570 | G | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.183+14280G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387570 | |||||||
chr2:241387606 | A | G | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.183+14316A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387606 | |||||||
chr2:241387661 | T | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+14371T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387661 | |||||||
chr2:241387705 | A | T | 1 | a0002c0002t0001g0352 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.183+14415A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387705 | |||||||
chr2:241387748 | G | A | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.183+14458G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387748 | |||||||
chr2:241387790 | CA | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(172): Show |
175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.183+14519delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241387790 | ||||||
chr2:241387803 | A | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+14513A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387803 | |||||||
chr2:241387809 | A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+14519A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387809 | |||||||
chr2:241387878 | C | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+14588C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387878 | |||||||
chr2:241388234 | T | C | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+14944T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388234 | |||||||
chr2:241388292 | G | A | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+15002G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388292 | |||||||
chr2:241388318 | A | C | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+15028A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388318 | |||||||
chr2:241388399 | C | T | 2 | a0003c0005t0001g0198 a0003c0005t0001g0199 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.183+15109C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388399 | |||||||
chr2:241388558 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.183+15268A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388558 | |||||||
chr2:241388662 | C | T | 1 | a0001c0011t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-15166C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388662 | |||||||
chr2:241388663 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-15165G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388663 | |||||||
chr2:241388840 | C | G | 4 | a0003c0005t0001g0042 a0003c0005t0001g0043 a0003c0005t0001g0044 others(1): Show |
4 | NA18953.hp2 NA18963.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-14988C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388840 | |||||||
chr2:241388973 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.184-14855T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388973 | |||||||
chr2:241388997 | G | A | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184-14831G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388997 | |||||||
chr2:241389270 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.184-14558C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241389270 | |||||||
chr2:241389991 | A | G | 16 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(13): Show |
16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.184-13837A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241389991 | |||||||
chr2:241390039 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.184-13789A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390039 | |||||||
chr2:241390086 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-13742C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390086 | |||||||
chr2:241390138 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.184-13690G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390138 | |||||||
chr2:241390174 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.184-13654C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390174 | |||||||
chr2:241390402 | A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.184-13426A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390402 | |||||||
chr2:241390663 | A | G | 4 | a0003c0005t0001g0042 a0003c0005t0001g0043 a0003c0005t0001g0044 others(1): Show |
4 | NA18953.hp2 NA18963.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-13165A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390663 | |||||||
chr2:241390777 | G | T | 291 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0158 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.184-13051G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390777 | |||||||
chr2:241390919 | T | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-12909T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390919 | |||||||
chr2:241390981 | C | G | 1 | a0002c0002t0001g0351 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.184-12847C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390981 | |||||||
chr2:241391336 | A | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-12492A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391336 | |||||||
chr2:241391700 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-12128C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391700 | |||||||
chr2:241391852 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.184-11976G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391852 | |||||||
chr2:241391860 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-11968G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391860 | |||||||
chr2:241391861 | C | A | 1 | a0001c0022t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.184-11967C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391861 | |||||||
chr2:241391907 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.184-11921T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391907 | |||||||
chr2:241392200 | C | T | 4 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-11628C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392200 | |||||||
chr2:241392272 | G | A | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184-11556G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392272 | |||||||
chr2:241392796 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-11032A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392796 | |||||||
chr2:241392842 | C | T | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-10986C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392842 | |||||||
chr2:241392949 | G | GA | 30 | a0001c0001t0001g0209 a0003c0005t0001g0010 a0003c0005t0001g0039 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.184-10868dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241392949 | ||||||
chr2:241393023 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.184-10805T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393023 | |||||||
chr2:241393180 | C | T | 42 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0237 others(39): Show |
42 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-10648C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393180 | |||||||
chr2:241393300 | G | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-10528G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393300 | |||||||
chr2:241393300 | G | T | 33 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(30): Show |
33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.184-10528G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393300 | |||||||
chr2:241393340 | A | G | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.184-10488A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393340 | |||||||
chr2:241393575 | C | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184-10253C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393575 | |||||||
chr2:241393661 | A | G | 1 | a0001c0004t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-10167A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393661 | |||||||
chr2:241393709 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.184-10119A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393709 | |||||||
chr2:241393775 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-10053A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393775 | |||||||
chr2:241393999 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-9829G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393999 | |||||||
chr2:241394055 | T | C | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-9773T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394055 | |||||||
chr2:241394058 | A | C | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-9770A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394058 | |||||||
chr2:241394171 | G | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-9657G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394171 | |||||||
chr2:241394387 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.184-9441G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394387 | |||||||
chr2:241394474 | C | A | 99 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.184-9354C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394474 | |||||||
chr2:241394517 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-9311C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394517 | |||||||
chr2:241394517 | C | CA | 30 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0133 others(27): Show |
30 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.184-9294dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241394517 | ||||||
chr2:241394517 | CA | C | 52 | a0001c0001t0001g0201 a0001c0001t0001g0303 a0001c0001t0001g0377 others(49): Show |
52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.184-9294delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241394517 | ||||||
chr2:241394605 | C | T | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-9223C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394605 | |||||||
chr2:241394920 | G | A | 110 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.184-8908G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394920 | |||||||
chr2:241395034 | G | T | 1 | a0001c0006t0001g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.184-8794G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395034 | |||||||
chr2:241395044 | A | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-8784A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395044 | |||||||
chr2:241395080 | G | A | 1 | a0003c0005t0001g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.184-8748G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395080 | |||||||
chr2:241395093 | A | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.184-8735A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395093 | |||||||
chr2:241395187 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.184-8641C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395187 | |||||||
chr2:241395193 | G | T | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.184-8635G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395193 | |||||||
chr2:241395220 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184-8608G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395220 | |||||||
chr2:241395342 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.184-8486A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395342 | |||||||
chr2:241395550 | C | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-8278C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395550 | |||||||
chr2:241395760 | A | G | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.184-8068A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395760 | |||||||
chr2:241395928 | G | A | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-7900G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395928 | |||||||
chr2:241396009 | T | C | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-7819T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396009 | |||||||
chr2:241396044 | T | A | 1 | a0001c0001t0001g0283 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.184-7784T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396044 | |||||||
chr2:241396095 | G | C | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-7733G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396095 | |||||||
chr2:241396270 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.184-7558A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396270 | |||||||
chr2:241396345 | A | C | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-7483A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396345 | |||||||
chr2:241396425 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-7403A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396425 | |||||||
chr2:241396507 | T | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG00733.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.184-7321T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396507 | |||||||
chr2:241396517 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.184-7311G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396517 | |||||||
chr2:241396587 | T | G | 2 | a0001c0006t0001g0244 a0001c0006t0001g0245 |
2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.184-7241T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396587 | |||||||
chr2:241396625 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-7203C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396625 | |||||||
chr2:241396884 | C | T | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.184-6944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396884 | |||||||
chr2:241396958 | G | GATTAAGA others(11): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-6867_184-6850d others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241396958 | ||||||
chr2:241396984 | G | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-6844G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396984 | |||||||
chr2:241396996 | A | G | 1 | a0001c0004t0001g0179 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.184-6832A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396996 | |||||||
chr2:241397030 | T | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-6798T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397030 | |||||||
chr2:241397143 | G | A | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-6685G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397143 | |||||||
chr2:241397192 | G | C | 1 | a0003c0005t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.184-6636G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397192 | |||||||
chr2:241397199 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.184-6629G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397199 | |||||||
chr2:241397441 | C | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.184-6387C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397441 | |||||||
chr2:241397791 | C | G | 2 | a0003c0005t0001g0046 a0003c0005t0001g0047 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.184-6037C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397791 | |||||||
chr2:241397831 | C | CT | 53 | a0001c0001t0001g0133 a0001c0001t0001g0204 a0001c0001t0001g0217 others(50): Show |
53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.184-5979dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | ||||||
chr2:241397831 | C | CTT | 28 | a0002c0002t0001g0343 a0002c0002t0001g0357 a0003c0005t0001g0010 others(25): Show |
28 | HG00099.hp1 HG01123.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.184-5980_184-5979d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | ||||||
chr2:241397831 | CT | C | 79 | a0001c0001t0001g0158 a0001c0001t0001g0366 a0001c0001t0001g0367 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-5979delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | ||||||
chr2:241397868 | C | T | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.184-5960C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397868 | |||||||
chr2:241397884 | C | T | 17 | a0001c0004t0001g0165 a0001c0004t0001g0166 a0001c0004t0001g0167 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.184-5944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397884 | |||||||
chr2:241397974 | C | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-5854C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397974 | |||||||
chr2:241397996 | A | AT | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-5824dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397996 | ||||||
chr2:241398021 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184-5807T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398021 | |||||||
chr2:241398036 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.184-5792T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398036 | |||||||
chr2:241398218 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184-5610A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398218 | |||||||
chr2:241398233 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-5595T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398233 | |||||||
chr2:241398245 | C | T | 1 | a0001c0003t0001g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.184-5583C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398245 | |||||||
chr2:241398268 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184-5560C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398268 | |||||||
chr2:241398307 | G | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.184-5521G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398307 | |||||||
chr2:241398428 | G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.184-5400G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398428 | |||||||
chr2:241398572 | C | CT | 40 | a0001c0001t0001g0005 a0002c0002t0001g0200 a0002c0002t0001g0253 others(37): Show |
40 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.184-5241dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398572 | ||||||
chr2:241398572 | C | CTT | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.184-5242_184-5241d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398572 | ||||||
chr2:241398666 | T | C | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184-5162T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398666 | |||||||
chr2:241398812 | G | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-5016G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398812 | |||||||
chr2:241398838 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.184-4990G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398838 | |||||||
chr2:241398876 | C | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-4952C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398876 | |||||||
chr2:241398899 | A | G | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-4929A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398899 | |||||||
chr2:241398980 | ATAC | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184-4846_184-4844d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398980 | ||||||
chr2:241399220 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.184-4608C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399220 | |||||||
chr2:241399394 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.184-4434T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399394 | |||||||
chr2:241399431 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.184-4397A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399431 | |||||||
chr2:241399733 | G | T | 1 | a0001c0003t0001g0027 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-4095G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399733 | |||||||
chr2:241399802 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-4026G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399802 | |||||||
chr2:241399988 | CTG | C | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-3837_184-3836d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241399988 | ||||||
chr2:241400027 | G | A | 2 | a0001c0004t0001g0359 a0001c0004t0001g0360 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-3801G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400027 | |||||||
chr2:241400059 | G | C | 2 | a0001c0003t0001g0020 a0001c0003t0001g0021 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.184-3769G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400059 | |||||||
chr2:241400120 | G | T | 1 | a0001c0006t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.184-3708G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400120 | |||||||
chr2:241400170 | G | C | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184-3658G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400170 | |||||||
chr2:241400229 | A | AAG | 221 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(218): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.184-3598_184-3597d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241400229 | ||||||
chr2:241400234 | T | G | 290 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.184-3594T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400234 | |||||||
chr2:241400241 | A | G | 84 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(81): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.184-3587A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400241 | |||||||
chr2:241400321 | G | C | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-3507G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400321 | |||||||
chr2:241401125 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2703G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401125 | |||||||
chr2:241401259 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2569C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401259 | |||||||
chr2:241401573 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-2255G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401573 | |||||||
chr2:241401662 | T | A | 1 | a0001c0003t0001g0027 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-2166T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401662 | |||||||
chr2:241401806 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184-2022C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401806 | |||||||
chr2:241401807 | G | A | 1 | a0013c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.184-2021G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401807 | |||||||
chr2:241401818 | C | CTT | 290 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.184-2010_184-2009i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401818 | |||||||
chr2:241401844 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.184-1984G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401844 | |||||||
chr2:241402021 | C | T | 2 | a0001c0004t0001g0359 a0001c0004t0001g0360 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402021 | |||||||
chr2:241402091 | A | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-1737A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402091 | |||||||
chr2:241402159 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.184-1669G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402159 | |||||||
chr2:241402485 | G | A | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.184-1343G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402485 | |||||||
chr2:241402834 | A | ATT | 7 | a0001c0001t0001g0283 a0001c0001t0001g0296 a0001c0001t0001g0307 others(4): Show |
7 | HG00099.hp1 HG01993.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-992_184-991dup others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402834 | ||||||
chr2:241402836 | T | TTATA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0141 |
3 | HG04228.hp1 HG04228.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.184-950_184-947dup others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0135 a0001c0001t0001g0188 a0001c0011t0001g0108 |
3 | HG00544.hp1 HG00558.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.184-954_184-947dup others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTATATAT others(3): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0010c0020t0001g0155 |
3 | HG00323.hp1 HG02135.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.184-956_184-947dup others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTATATAT others(5): Show |
1 | a0001c0019t0001g0111 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.184-958_184-947dup others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTATATAT others(9): Show |
1 | a0001c0022t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.184-962_184-947dup others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTTTATAT others(5): Show |
2 | a0001c0001t0001g0204 a0003c0005t0001g0051 |
2 | HG03669.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.184-991_184-990ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | T | TTTTATAT others(13): Show |
3 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0012c0030t0001g0006 |
3 | HG02486.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.184-991_184-990ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTA | T | 11 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(8): Show |
11 | HG00408.hp2 HG00733.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-948_184-947del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0223 a0001c0004t0001g0164 a0003c0005t0001g0057 |
3 | HG01123.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.184-956_184-947del others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTATATAT others(5): Show |
T | 9 | a0001c0001t0001g0368 a0001c0004t0001g0162 a0001c0004t0001g0163 others(6): Show |
9 | HG00642.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-958_184-947del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTATATAT others(11): Show |
T | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.184-964_184-947del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTATATAT others(13): Show |
T | 11 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0020 others(8): Show |
11 | HG01255.hp2 HG02129.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-966_184-947del others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402836 | TTATATAT others(17): Show |
T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-970_184-947del others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | ||||||
chr2:241402838 | A | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.184-990A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402838 | |||||||
chr2:241402840 | A | T | 6 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0319 others(3): Show |
6 | HG00408.hp2 HG00733.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-988A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402840 | |||||||
chr2:241402844 | A | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.184-984A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402844 | |||||||
chr2:241402844 | A | T | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.184-984A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402844 | |||||||
chr2:241402845 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402845 | ||||||
chr2:241402845 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0080 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.184-964_184-963ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402845 | ||||||
chr2:241402846 | A | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-982A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402846 | |||||||
chr2:241402847 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0079 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.184-968_184-967ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402847 | ||||||
chr2:241402847 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.184-966_184-965ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402847 | ||||||
chr2:241402848 | A | T | 2 | a0001c0004t0001g0164 a0003c0005t0001g0057 |
2 | HG01123.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.184-980A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402848 | |||||||
chr2:241402849 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402849 | ||||||
chr2:241402850 | A | T | 8 | a0001c0004t0001g0162 a0001c0004t0001g0163 a0001c0004t0001g0168 others(5): Show |
8 | HG00642.hp1 HG01169.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-978A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402850 | |||||||
chr2:241402853 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402853 | ||||||
chr2:241402856 | A | T | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.184-972A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402856 | |||||||
chr2:241402858 | A | T | 11 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0020 others(8): Show |
11 | HG01255.hp2 HG02129.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-970A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402858 | |||||||
chr2:241402858 | ATATATAT others(21): Show |
A | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.184-968_184-941del others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402858 | ||||||
chr2:241402859 | TATATATA others(10): Show |
T | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184-968_184-952del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402859 | |||||||
chr2:241402859 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.184-968_184-950del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402859 | |||||||
chr2:241402860 | A | C | 35 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0256 others(32): Show |
35 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.184-968A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402860 | |||||||
chr2:241402860 | ATATATAT others(14): Show |
A | 2 | a0007c0028t0001g0018 a0013c0031t0001g0019 |
2 | HG02055.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.184-966_184-946del others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402860 | ||||||
chr2:241402861 | TATATATA others(12): Show |
T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0036 |
2 | HG00609.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.184-966_184-948del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402861 | |||||||
chr2:241402862 | A | C | 1 | a0002c0002t0001g0254 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.184-966A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402862 | |||||||
chr2:241402862 | ATATATAT others(12): Show |
A | 2 | a0001c0003t0001g0023 a0001c0003t0001g0060 |
2 | HG01192.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.184-964_184-946del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402862 | ||||||
chr2:241402862 | ATATATAT others(13): Show |
A | 9 | a0001c0001t0001g0125 a0001c0003t0001g0007 a0001c0003t0001g0022 others(6): Show |
9 | HG00280.hp1 HG01106.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-964_184-945del others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402862 | ||||||
chr2:241402863 | T | C | 21 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0067 others(18): Show |
21 | HG00280.hp2 HG00323.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.184-965T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402863 | |||||||
chr2:241402863 | TATATATA others(10): Show |
T | 3 | a0001c0001t0001g0312 a0001c0001t0001g0378 a0001c0003t0001g0008 |
3 | HG02083.hp1 HG02258.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.184-964_184-948del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402863 | |||||||
chr2:241402864 | ATATATAT others(11): Show |
A | 5 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0014 others(2): Show |
5 | HG03486.hp1 NA18955.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-962_184-945del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402864 | ||||||
chr2:241402864 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0269 a0005c0008t0001g0147 |
2 | HG02451.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.184-962_184-944del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402864 | ||||||
chr2:241402865 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.184-963T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402865 | |||||||
chr2:241402866 | ATATATAT others(9): Show |
A | 2 | a0005c0008t0001g0153 a0005c0008t0001g0154 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.184-960_184-945del others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402866 | ||||||
chr2:241402866 | ATATATAT others(10): Show |
A | 1 | a0005c0008t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.184-960_184-944del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402866 | ||||||
chr2:241402867 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0091 |
2 | HG02071.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.184-961T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | |||||||
chr2:241402867 | TATATATA others(4): Show |
T | 5 | a0003c0005t0001g0192 a0003c0005t0001g0195 a0003c0005t0001g0196 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-960_184-950del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | |||||||
chr2:241402867 | TATATATA others(6): Show |
T | 1 | a0006c0009t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.184-960_184-948del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | |||||||
chr2:241402868 | ATATATAT others(6): Show |
A | 1 | a0001c0004t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.184-958_184-946del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | ||||||
chr2:241402868 | ATATATAT others(7): Show |
A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.184-958_184-945del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | ||||||
chr2:241402868 | ATATATAT others(8): Show |
A | 1 | a0001c0003t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.184-958_184-944del others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | ||||||
chr2:241402868 | ATATATAT others(9): Show |
A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.184-958_184-943del others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | ||||||
chr2:241402868 | ATATATAT others(12): Show |
A | 2 | a0001c0006t0001g0246 a0001c0006t0001g0251 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.184-958_184-940del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | ||||||
chr2:241402869 | TATATATA others(4): Show |
T | 2 | a0003c0005t0001g0045 a0003c0005t0001g0193 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.184-958_184-948del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402869 | |||||||
chr2:241402870 | ATATATAT others(4): Show |
A | 5 | a0001c0025t0001g0160 a0003c0005t0001g0197 a0006c0009t0001g0183 others(2): Show |
5 | HG01123.hp2 HG01168.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-956_184-946del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | ||||||
chr2:241402870 | ATATATAT others(5): Show |
A | 4 | a0001c0004t0001g0166 a0001c0004t0001g0167 a0001c0004t0001g0179 others(1): Show |
4 | HG01433.hp2 HG03017.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-956_184-945del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | ||||||
chr2:241402870 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.184-956_184-943del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | ||||||
chr2:241402870 | ATATATAT others(11): Show |
A | 1 | a0001c0006t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.184-956_184-939del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | ||||||
chr2:241402870 | ATATATAT others(12): Show |
A | 3 | a0001c0006t0001g0236 a0001c0006t0001g0247 a0001c0006t0001g0248 |
3 | NA18984.hp2 NA19077.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.184-956_184-938del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | ||||||
chr2:241402872 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.184-956A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402872 | |||||||
chr2:241402872 | ATATATAT others(4): Show |
A | 2 | a0001c0004t0001g0177 a0001c0004t0001g0180 |
2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.184-954_184-944del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | ||||||
chr2:241402872 | ATATATAT others(5): Show |
A | 2 | a0001c0004t0001g0178 a0001c0004t0001g0181 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.184-954_184-943del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | ||||||
chr2:241402872 | ATATATAT others(7): Show |
A | 2 | a0001c0006t0001g0241 a0001c0006t0001g0250 |
2 | HG02056.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.184-954_184-941del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | ||||||
chr2:241402874 | ATATATAT others(4): Show |
A | 2 | a0002c0002t0001g0257 a0002c0002t0001g0358 |
2 | HG02080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.184-952_184-942del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | ||||||
chr2:241402874 | ATATATAT others(5): Show |
A | 9 | a0002c0002t0001g0253 a0002c0002t0001g0258 a0002c0002t0001g0259 others(6): Show |
9 | HG00609.hp2 NA18942.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-952_184-941del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | ||||||
chr2:241402874 | ATATATAT others(6): Show |
A | 2 | a0001c0006t0001g0244 a0002c0002t0001g0200 |
2 | HG00408.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.184-952_184-940del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | ||||||
chr2:241402874 | ATATATAT others(8): Show |
A | 1 | a0001c0006t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.184-952_184-938del others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | ||||||
chr2:241402875 | TATA | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0313 a0007c0021t0003g0334 |
3 | HG00140.hp2 HG01070.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.184-952_184-950del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402875 | |||||||
chr2:241402876 | A | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0306 a0001c0004t0001g0157 others(1): Show |
4 | HG00738.hp1 HG01516.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-952A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402876 | |||||||
chr2:241402876 | ATATATTT others(3): Show |
A | 3 | a0002c0002t0001g0254 a0002c0002t0001g0260 a0011c0017t0001g0255 |
3 | HG00597.hp1 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.184-950_184-941del others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | ||||||
chr2:241402876 | ATATATTT others(4): Show |
A | 3 | a0002c0002t0001g0256 a0002c0002t0001g0261 a0002c0002t0001g0340 |
3 | HG00639.hp1 HG02293.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.184-950_184-940del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | ||||||
chr2:241402876 | ATATATTT others(5): Show |
A | 14 | a0002c0002t0001g0335 a0002c0002t0001g0339 a0002c0002t0001g0341 others(11): Show |
14 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.184-950_184-939del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | ||||||
chr2:241402876 | ATATATTT others(6): Show |
A | 2 | a0001c0006t0001g0245 a0002c0002t0001g0350 |
2 | HG00597.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.184-950_184-938del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | ||||||
chr2:241402878 | A | T | 20 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0216 others(17): Show |
20 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.184-950A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402878 | |||||||
chr2:241402878 | ATAT | A | 7 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0001g0279 others(4): Show |
7 | NA18960.hp2 NA18971.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-948_184-946del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402878 | ||||||
chr2:241402878 | ATATTTTT others(4): Show |
A | 4 | a0001c0006t0001g0242 a0002c0002t0001g0342 a0002c0002t0001g0343 others(1): Show |
4 | HG00621.hp2 HG01175.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-948_184-938del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402878 | ||||||
chr2:241402879 | TA | T | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0004g0265 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-948delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402879 | |||||||
chr2:241402880 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0207 a0001c0001t0001g0213 |
2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0303 |
2 | HG01891.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0082 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(27): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0224 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(19): Show |
1 | a0004c0007t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0212 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(17): Show |
1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0206 |
2 | HG03942.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0209 |
2 | NA18971.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(10): Show |
8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG02056.hp2 HG03927.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0085 a0001c0001t0001g0090 |
3 | HG01934.hp1 NA18962.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | NA18979.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(13): Show |
1 | a0004c0007t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0137 a0003c0005t0001g0052 others(1): Show |
4 | HG02074.hp1 HG02559.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0071 a0003c0005t0003g0058 |
2 | HG02004.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0222 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0232 a0003c0005t0001g0044 |
2 | HG02257.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(5): Show |
1 | a0001c0003t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0210 a0004c0007t0001g0130 |
2 | HG01109.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATAT others(3): Show |
2 | a0001c0011t0001g0107 a0003c0005t0001g0369 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATTT others(3): Show |
1 | a0004c0007t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | ||||||
chr2:241402880 | A | T | 55 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(52): Show |
55 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.184-948A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402880 | |||||||
chr2:241402881 | T | TA | 4 | a0001c0001t0001g0298 a0001c0001t0002g0373 a0008c0013t0001g0029 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(1): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATA | 5 | a0001c0001t0001g0113 a0001c0001t0001g0268 a0001c0001t0001g0285 others(2): Show |
5 | HG00558.hp2 HG02735.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATA | 5 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0003t0001g0053 others(2): Show |
5 | HG01243.hp2 HG01928.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0120 a0001c0001t0001g0284 |
3 | HG02074.hp2 HG03491.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(4): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0208 a0001c0001t0002g0375 |
3 | HG00544.hp2 HG02572.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0302 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402881 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(23): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | |||||||
chr2:241402882 | T | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0123 others(14): Show |
17 | HG00323.hp1 HG00558.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.184-946T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402882 | |||||||
chr2:241402883 | T | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0120 a0001c0001t0001g0124 others(10): Show |
13 | HG00558.hp2 HG01168.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.184-945T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402883 | |||||||
chr2:241402884 | T | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0229 a0001c0001t0001g0278 others(5): Show |
8 | HG00323.hp1 HG02027.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-944T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402884 | |||||||
chr2:241402885 | T | A | 9 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0001t0001g0235 others(6): Show |
9 | HG01928.hp1 HG02572.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-943T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402885 | |||||||
chr2:241402886 | T | A | 2 | a0001c0001t0001g0229 a0001c0004t0001g0143 |
2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-942T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402886 | |||||||
chr2:241402887 | T | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0235 a0001c0001t0001g0333 others(1): Show |
4 | HG02965.hp2 HG03017.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-941T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402887 | |||||||
chr2:241402888 | T | A | 2 | a0001c0001t0001g0229 a0001c0004t0001g0143 |
2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-940T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402888 | |||||||
chr2:241402889 | T | A | 2 | a0001c0001t0001g0142 a0015c0023t0001g0203 |
2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-939T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402889 | |||||||
chr2:241402890 | T | A | 2 | a0001c0001t0001g0229 a0001c0004t0001g0143 |
2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-938T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402890 | |||||||
chr2:241402891 | T | A | 2 | a0001c0001t0001g0142 a0015c0023t0001g0203 |
2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-937T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402891 | |||||||
chr2:241402892 | T | A | 2 | a0001c0001t0001g0229 a0001c0004t0001g0143 |
2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-936T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402892 | |||||||
chr2:241402893 | T | A | 2 | a0001c0001t0001g0142 a0015c0023t0001g0203 |
2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-935T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402893 | |||||||
chr2:241402895 | T | A | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184-933T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402895 | |||||||
chr2:241402911 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.184-917T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402911 | |||||||
chr2:241402964 | C | G | 26 | a0001c0001t0001g0268 a0001c0001t0001g0304 a0001c0001t0001g0305 others(23): Show |
26 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.184-864C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402964 | |||||||
chr2:241403254 | A | G | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.184-574A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403254 | |||||||
chr2:241403353 | T | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.184-475T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403353 | |||||||
chr2:241403375 | C | T | 2 | a0001c0006t0001g0246 a0001c0006t0001g0251 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.184-453C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403375 | |||||||
chr2:241403505 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-323C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403505 | |||||||
chr2:241403543 | C | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-285C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403543 | |||||||
chr2:241403569 | T | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.184-259T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403569 | |||||||
chr2:241403989 | C | T | 29 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(26): Show |
29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.288+57C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241403989 | |||||||
chr2:241404058 | G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.288+126G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404058 | |||||||
chr2:241404201 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.288+269C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404201 | |||||||
chr2:241404289 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.288+357T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404289 | |||||||
chr2:241404380 | C | A | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.289-419C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404380 | |||||||
chr2:241404388 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.289-411T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404388 | |||||||
chr2:241404622 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.289-177G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404622 | |||||||
chr2:241404670 | G | C | 2 | a0003c0005t0001g0046 a0003c0005t0001g0047 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.289-129G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404670 | |||||||
chr2:241404713 | T | C | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.289-86T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404713 | |||||||
chr2:241404754 | G | T | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289-45G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404754 | |||||||
chr2:241404918 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.331+77A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241404918 | |||||||
chr2:241404969 | C | T | 1 | a0001c0003t0001g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.331+128C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241404969 | |||||||
chr2:241405078 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.331+237G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405078 | |||||||
chr2:241405184 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.331+343T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405184 | |||||||
chr2:241405261 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.331+420C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405261 | |||||||
chr2:241405280 | T | C | 4 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0004t0001g0171 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+439T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405280 | |||||||
chr2:241405370 | C | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.331+529C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405370 | |||||||
chr2:241405371 | G | A | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.331+530G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405371 | |||||||
chr2:241405434 | A | G | 5 | a0005c0008t0001g0147 a0005c0008t0001g0151 a0005c0008t0001g0153 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+593A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405434 | |||||||
chr2:241405452 | T | A | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+611T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405452 | |||||||
chr2:241405507 | A | G | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.331+666A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405507 | |||||||
chr2:241405622 | A | T | 1 | a0001c0001t0001g0295 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.331+781A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405622 | |||||||
chr2:241405715 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.331+874C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405715 | |||||||
chr2:241405725 | G | A | 6 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0003c0005t0001g0049 others(3): Show |
6 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+884G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405725 | |||||||
chr2:241405745 | C | T | 1 | a0002c0002t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.331+904C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405745 | |||||||
chr2:241405795 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.331+954G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405795 | |||||||
chr2:241405802 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.331+961C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405802 | |||||||
chr2:241405817 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.331+976T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405817 | |||||||
chr2:241405865 | C | T | 1 | a0002c0002t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.331+1024C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405865 | |||||||
chr2:241405891 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.331+1050A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405891 | |||||||
chr2:241405938 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.331+1097A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405938 | |||||||
chr2:241405972 | T | A | 2 | a0003c0005t0001g0195 a0016c0027t0001g0145 |
2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331+1131T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405972 | |||||||
chr2:241406086 | A | C | 9 | a0001c0001t0001g0098 a0001c0001t0002g0372 a0001c0004t0001g0359 others(6): Show |
9 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+1245A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406086 | |||||||
chr2:241406099 | C | T | 31 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+1258C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406099 | |||||||
chr2:241406114 | T | C | 3 | a0001c0001t0001g0329 a0001c0004t0001g0168 a0003c0005t0001g0194 |
3 | HG01934.hp2 HG02895.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.331+1273T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406114 | |||||||
chr2:241406119 | T | C | 41 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0205 others(38): Show |
41 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.331+1278T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406119 | |||||||
chr2:241406128 | T | C | 5 | a0001c0004t0001g0178 a0001c0004t0001g0180 a0001c0004t0001g0181 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+1287T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406128 | |||||||
chr2:241406132 | C | T | 12 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0119 others(9): Show |
12 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+1291C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406132 | |||||||
chr2:241406157 | G | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0116 others(14): Show |
17 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+1316G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406157 | |||||||
chr2:241406179 | G | A | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.331+1338G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406179 | |||||||
chr2:241406200 | C | T | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.332-1337C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406200 | |||||||
chr2:241406257 | G | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-1280G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406257 | |||||||
chr2:241406265 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.332-1272G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406265 | |||||||
chr2:241406367 | TTA | T | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
9 | HG00639.hp2 HG01167.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.332-1156_332-1155d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406367 | ||||||
chr2:241406411 | G | GTA | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0188 others(1): Show |
4 | HG00558.hp1 HG02083.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1117_332-1116d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406411 | ||||||
chr2:241406420 | T | TAG | 13 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0004c0007t0001g0096 others(10): Show |
13 | HG01099.hp1 HG01109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-1100_332-1099d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406420 | ||||||
chr2:241406420 | TAG | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(225): Show |
228 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.332-1100_332-1099d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406420 | ||||||
chr2:241406422 | G | T | 86 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0003t0001g0007 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.332-1115G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406422 | |||||||
chr2:241406424 | G | T | 142 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(139): Show |
142 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.332-1113G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406424 | |||||||
chr2:241406426 | G | T | 73 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(70): Show |
73 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.332-1111G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406426 | |||||||
chr2:241406628 | G | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-909G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406628 | |||||||
chr2:241406630 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-907G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406630 | |||||||
chr2:241406642 | C | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-895C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406642 | |||||||
chr2:241406642 | C | T | 25 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.332-895C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406642 | |||||||
chr2:241406655 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.332-882G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406655 | |||||||
chr2:241406831 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-706G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406831 | |||||||
chr2:241406876 | C | T | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.332-661C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406876 | |||||||
chr2:241406941 | G | C | 1 | a0001c0003t0001g0027 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.332-596G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406941 | |||||||
chr2:241406965 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.332-572G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406965 | |||||||
chr2:241406968 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.332-569C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406968 | |||||||
chr2:241406991 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-546A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406991 | |||||||
chr2:241407001 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-536G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407001 | |||||||
chr2:241407009 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0366 a0001c0001t0001g0367 |
3 | HG01167.hp1 HG01169.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.332-528T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407009 | |||||||
chr2:241407010 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407010 | |||||||
chr2:241407011 | T | G | 17 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(14): Show |
17 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-526T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407011 | |||||||
chr2:241407012 | G | A | 5 | a0001c0001t0001g0109 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-525G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | |||||||
chr2:241407012 | G | C | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.332-525G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | |||||||
chr2:241407012 | G | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.332-525G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | |||||||
chr2:241407019 | A | G | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.332-518A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407019 | |||||||
chr2:241407056 | C | G | 95 | a0001c0001t0001g0223 a0001c0001t0001g0268 a0001c0001t0001g0304 others(92): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.332-481C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407056 | |||||||
chr2:241407090 | G | C | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.332-447G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407090 | |||||||
chr2:241407100 | G | T | 1 | a0001c0001t0005g0126 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.332-437G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407100 | |||||||
chr2:241407104 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.332-433A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407104 | |||||||
chr2:241407118 | T | C | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.332-419T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407118 | |||||||
chr2:241407788 | A | G | 2 | a0001c0001t0001g0071 a0019c0024t0001g0087 |
2 | NA18970.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.410+173A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241407788 | |||||||
chr2:241408049 | G | T | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+434G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408049 | |||||||
chr2:241408186 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.410+571A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408186 | |||||||
chr2:241408199 | C | T | 20 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(17): Show |
20 | HG00099.hp1 HG01123.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+584C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408199 | |||||||
chr2:241408243 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.410+628G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408243 | |||||||
chr2:241408307 | G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.410+692G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408307 | |||||||
chr2:241408466 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.410+851C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408466 | |||||||
chr2:241408492 | G | A | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.410+877G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408492 | |||||||
chr2:241408541 | CA | C | 228 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.410+941delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241408541 | ||||||
chr2:241408541 | CAA | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0085 a0001c0001t0001g0201 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.410+940_410+941del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241408541 | ||||||
chr2:241408556 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+941A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408556 | |||||||
chr2:241408577 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.410+962C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408577 | |||||||
chr2:241408667 | C | T | 1 | a0004c0007t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.410+1052C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408667 | |||||||
chr2:241408756 | A | G | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.410+1141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408756 | |||||||
chr2:241408835 | G | A | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.410+1220G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408835 | |||||||
chr2:241408858 | T | C | 4 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+1243T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408858 | |||||||
chr2:241409004 | A | G | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.410+1389A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409004 | |||||||
chr2:241409038 | T | TGATA | 145 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(142): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.410+1460_410+1463d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | ||||||
chr2:241409038 | T | TGATAGAT others(1): Show |
82 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0086 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.410+1456_410+1463d others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | ||||||
chr2:241409038 | T | TGATAGAT others(5): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.410+1452_410+1463d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | ||||||
chr2:241409038 | T | TGATAGAT others(9): Show |
2 | a0001c0001t0001g0098 a0003c0005t0001g0194 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.410+1448_410+1463d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | ||||||
chr2:241409038 | TGATA | T | 30 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0004t0001g0177 others(27): Show |
30 | HG00597.hp1 HG01243.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.410+1460_410+1463d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | ||||||
chr2:241409199 | AT | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.410+1586delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409199 | ||||||
chr2:241409245 | T | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.410+1630T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409245 | |||||||
chr2:241409416 | G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.411-1617G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409416 | |||||||
chr2:241409506 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.411-1527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409506 | |||||||
chr2:241409831 | T | C | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.411-1202T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409831 | |||||||
chr2:241409846 | A | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-1187A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409846 | |||||||
chr2:241409852 | C | T | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-1181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409852 | |||||||
chr2:241409918 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.411-1115A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409918 | |||||||
chr2:241409932 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.411-1101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409932 | |||||||
chr2:241410038 | CAG | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-994_411-993del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410038 | |||||||
chr2:241410043 | G | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.411-990G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410043 | |||||||
chr2:241410182 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-851T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410182 | |||||||
chr2:241410233 | C | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.411-800C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410233 | |||||||
chr2:241410237 | C | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-796C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410237 | |||||||
chr2:241410238 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.411-795C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410238 | |||||||
chr2:241410388 | A | G | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.411-645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410388 | |||||||
chr2:241410433 | C | CT | 260 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.411-586dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241410433 | ||||||
chr2:241410478 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.411-555A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410478 | |||||||
chr2:241410479 | T | C | 4 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(1): Show |
4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-554T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410479 | |||||||
chr2:241410650 | G | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.411-383G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410650 | |||||||
chr2:241410677 | G | GC | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(6): Show |
9 | HG00423.hp1 HG02056.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.411-352dupC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241410677 | ||||||
chr2:241410743 | T | A | 6 | a0001c0003t0001g0007 a0001c0003t0001g0022 a0001c0003t0001g0023 others(3): Show |
6 | NA18949.hp2 NA18951.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-290T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410743 | |||||||
chr2:241410892 | G | A | 1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.411-141G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410892 | |||||||
chr2:241410938 | A | C | 4 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0163 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-95A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410938 | |||||||
chr2:241410974 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-59A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410974 | |||||||
chr2:241411190 | T | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+60T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411190 | |||||||
chr2:241411215 | T | G | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.508+85T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411215 | |||||||
chr2:241411367 | G | A | 2 | a0001c0006t0001g0246 a0001c0006t0001g0251 |
2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.508+237G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411367 | |||||||
chr2:241411506 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.508+376C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411506 | |||||||
chr2:241411522 | A | G | 372 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(369): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.508+392A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411522 | |||||||
chr2:241411529 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.508+399A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411529 | |||||||
chr2:241411571 | C | T | 1 | a0001c0003t0001g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.508+441C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411571 | |||||||
chr2:241411595 | A | G | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.508+465A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411595 | |||||||
chr2:241411651 | A | G | 290 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.508+521A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411651 | |||||||
chr2:241411740 | C | G | 1 | a0005c0008t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508+610C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411740 | |||||||
chr2:241411816 | G | A | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.508+686G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411816 | |||||||
chr2:241411860 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508+730A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411860 | |||||||
chr2:241411964 | T | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.508+834T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411964 | |||||||
chr2:241411970 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.508+840G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411970 | |||||||
chr2:241412065 | C | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.508+935C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412065 | |||||||
chr2:241412224 | C | G | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.509-1083C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412224 | |||||||
chr2:241412264 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.509-1043C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412264 | |||||||
chr2:241412398 | A | G | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.509-909A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412398 | |||||||
chr2:241412471 | A | C | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.509-836A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412471 | |||||||
chr2:241412630 | C | G | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.509-677C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412630 | |||||||
chr2:241412642 | A | T | 1 | a0005c0008t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-665A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412642 | |||||||
chr2:241412693 | A | G | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.509-614A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412693 | |||||||
chr2:241412760 | C | T | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-547C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412760 | |||||||
chr2:241412831 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.509-476C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412831 | |||||||
chr2:241412842 | A | G | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.509-465A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412842 | |||||||
chr2:241413166 | T | C | 2 | a0003c0005t0001g0045 a0003c0005t0001g0048 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509-141T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413166 | |||||||
chr2:241413167 | A | T | 84 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(81): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.509-140A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413167 | |||||||
chr2:241413218 | A | AT | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.509-80dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr2 | 241413218 | ||||||
chr2:241413218 | A | T | 2 | a0001c0001t0001g0113 a0017c0026t0001g0118 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.509-89A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413218 | |||||||
chr2:241413762 | G | C | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+341G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413762 | |||||||
chr2:241413867 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.623+446A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413867 | |||||||
chr2:241413936 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.623+515G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413936 | |||||||
chr2:241413940 | C | CA | 6 | a0001c0001t0001g0088 a0001c0001t0002g0372 a0001c0001t0002g0373 others(3): Show |
6 | HG01261.hp2 HG02523.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+534dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241413940 | ||||||
chr2:241413940 | CA | C | 11 | a0001c0001t0001g0268 a0001c0003t0001g0035 a0003c0005t0001g0046 others(8): Show |
11 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+534delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241413940 | ||||||
chr2:241414078 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.623+657G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414078 | |||||||
chr2:241414289 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.623+868G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414289 | |||||||
chr2:241414409 | G | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+988G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414409 | |||||||
chr2:241414438 | T | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.623+1017T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414438 | |||||||
chr2:241414525 | A | G | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+1104A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414525 | |||||||
chr2:241414606 | C | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.623+1185C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414606 | |||||||
chr2:241414608 | G | A | 1 | a0003c0005t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+1187G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414608 | |||||||
chr2:241414715 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.623+1294A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414715 | |||||||
chr2:241414725 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.623+1304G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414725 | |||||||
chr2:241414752 | G | A | 6 | a0001c0001t0001g0271 a0001c0001t0002g0372 a0001c0001t0002g0373 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+1331G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414752 | |||||||
chr2:241414956 | A | G | 22 | a0001c0003t0001g0062 a0002c0002t0001g0200 a0002c0002t0001g0339 others(19): Show |
22 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.623+1535A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414956 | |||||||
chr2:241415088 | C | T | 1 | a0001c0003t0001g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.623+1667C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415088 | |||||||
chr2:241415181 | G | C | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+1760G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415181 | |||||||
chr2:241415217 | T | C | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.623+1796T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415217 | |||||||
chr2:241415232 | A | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+1811A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415232 | |||||||
chr2:241415235 | C | T | 1 | a0009c0012t0001g0002 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.623+1814C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415235 | |||||||
chr2:241415413 | A | G | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.623+1992A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415413 | |||||||
chr2:241415431 | C | G | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.623+2010C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415431 | |||||||
chr2:241415463 | A | C | 1 | a0003c0005t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+2042A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415463 | |||||||
chr2:241415564 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 others(80): Show |
83 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.623+2143C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415564 | |||||||
chr2:241415576 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.623+2155G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415576 | |||||||
chr2:241415779 | T | A | 1 | a0003c0005t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624-2183T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415779 | |||||||
chr2:241415885 | A | C | 1 | a0003c0005t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.624-2077A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415885 | |||||||
chr2:241415987 | T | TTC | 22 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0003t0001g0007 others(19): Show |
22 | HG00621.hp2 HG00639.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1973_624-1972d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415987 | ||||||
chr2:241415989 | C | CTCTCTG | 4 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0009c0012t0001g0001 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTCTG | 17 | a0001c0001t0001g0205 a0001c0001t0001g0209 a0001c0001t0001g0220 others(14): Show |
17 | HG00609.hp1 HG01106.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTCTGTG | 18 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0210 others(15): Show |
18 | HG00423.hp2 HG00544.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0001g0214 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.624-1972_624-1971i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTG | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0063 others(47): Show |
50 | HG00323.hp2 HG00423.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.624-1929_624-1928d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTGTG | 22 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0094 others(19): Show |
22 | HG00280.hp2 HG00544.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1931_624-1928d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTGTGTG | 25 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0124 others(22): Show |
25 | HG00558.hp1 HG01099.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.624-1933_624-1928d others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTGTGTGT others(1): Show |
6 | a0003c0005t0001g0045 a0003c0005t0001g0052 a0003c0005t0001g0059 others(3): Show |
6 | HG01496.hp2 HG01934.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-1935_624-1928d others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTGTGTGT others(3): Show |
6 | a0003c0005t0001g0039 a0003c0005t0001g0042 a0003c0005t0001g0046 others(3): Show |
6 | HG00099.hp1 HG02004.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-1937_624-1928d others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | C | CTGTGTGT others(5): Show |
1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.624-1939_624-1928d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTG | C | 19 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0092 others(16): Show |
19 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.624-1929_624-1928d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTGTG | C | 53 | a0001c0001t0001g0136 a0001c0001t0001g0201 a0001c0001t0001g0202 others(50): Show |
53 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.624-1931_624-1928d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTGTGTG | C | 22 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0262 others(19): Show |
22 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1933_624-1928d others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0378 a0005c0008t0001g0146 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.624-1941_624-1928d others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTGTGTGT others(13): Show |
C | 35 | a0001c0001t0001g0158 a0001c0001t0001g0309 a0001c0001t0001g0315 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.624-1947_624-1928d others(22): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415989 | CTGTGTGT others(15): Show |
C | 4 | a0001c0001t0001g0268 a0001c0001t0001g0312 a0001c0001t0001g0326 others(1): Show |
4 | HG02083.hp1 NA18747.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1949_624-1928d others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | ||||||
chr2:241415991 | G | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0237 a0001c0001t0001g0239 others(55): Show |
58 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.624-1971G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415991 | |||||||
chr2:241415993 | G | C | 52 | a0001c0001t0001g0206 a0001c0001t0001g0234 a0001c0001t0001g0238 others(49): Show |
52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.624-1969G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415993 | |||||||
chr2:241415994 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.624-1968T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415994 | |||||||
chr2:241415995 | G | C | 77 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(74): Show |
77 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.624-1967G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415995 | |||||||
chr2:241415997 | G | C | 24 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0262 others(21): Show |
24 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.624-1965G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415997 | |||||||
chr2:241415999 | G | C | 8 | a0001c0001t0001g0264 a0001c0004t0001g0359 a0001c0004t0001g0360 others(5): Show |
8 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.624-1963G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415999 | |||||||
chr2:241416001 | G | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-1961G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416001 | |||||||
chr2:241416005 | G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-1957G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416005 | |||||||
chr2:241416007 | G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-1955G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416007 | |||||||
chr2:241416011 | G | C | 4 | a0001c0001t0001g0309 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1951G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416011 | |||||||
chr2:241416013 | G | C | 4 | a0001c0001t0001g0268 a0001c0001t0001g0312 a0001c0001t0001g0326 others(1): Show |
4 | HG02083.hp1 NA18747.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1949G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416013 | |||||||
chr2:241416119 | CTG | C | 111 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(108): Show |
111 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.624-1836_624-1835d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241416119 | ||||||
chr2:241416137 | T | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-1825T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416137 | |||||||
chr2:241416254 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.624-1708G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416254 | |||||||
chr2:241416283 | A | G | 1 | a0020c0016t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.624-1679A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416283 | |||||||
chr2:241416286 | G | A | 29 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(26): Show |
29 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.624-1676G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416286 | |||||||
chr2:241416314 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.624-1648A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416314 | |||||||
chr2:241416321 | T | C | 1 | a0003c0005t0001g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.624-1641T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416321 | |||||||
chr2:241416343 | C | T | 1 | a0001c0001t0009g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624-1619C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416343 | |||||||
chr2:241416400 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0113 a0001c0001t0001g0131 others(2): Show |
5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-1562T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416400 | |||||||
chr2:241416432 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.624-1530A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416432 | |||||||
chr2:241416680 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.624-1282A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416680 | |||||||
chr2:241416710 | G | A | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.624-1252G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416710 | |||||||
chr2:241416779 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.624-1183C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416779 | |||||||
chr2:241416824 | G | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.624-1138G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416824 | |||||||
chr2:241417022 | C | T | 2 | a0001c0004t0001g0370 a0005c0008t0001g0151 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.624-940C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417022 | |||||||
chr2:241417025 | G | A | 4 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 others(1): Show |
4 | NA18972.hp1 NA18986.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.624-937G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417025 | |||||||
chr2:241417076 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624-886G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417076 | |||||||
chr2:241417085 | G | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.624-877G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417085 | |||||||
chr2:241417240 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.624-722G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417240 | |||||||
chr2:241417309 | G | A | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-653G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417309 | |||||||
chr2:241417310 | A | G | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-652A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417310 | |||||||
chr2:241417360 | T | C | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-602T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417360 | |||||||
chr2:241417361 | C | T | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-601C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417361 | |||||||
chr2:241417414 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417414 | |||||||
chr2:241417472 | G | A | 63 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.624-490G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417472 | |||||||
chr2:241417479 | C | T | 17 | a0001c0004t0001g0165 a0001c0004t0001g0166 a0001c0004t0001g0167 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.624-483C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417479 | |||||||
chr2:241417588 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.624-374G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417588 | |||||||
chr2:241417642 | A | AT | 275 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(272): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.624-318dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241417642 | ||||||
chr2:241417694 | G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.624-268G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417694 | |||||||
chr2:241417900 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.624-62C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417900 | |||||||
chr2:241418188 | T | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+79T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418188 | |||||||
chr2:241418268 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771+159C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418268 | |||||||
chr2:241418393 | C | G | 4 | a0001c0004t0001g0362 a0001c0010t0001g0363 a0001c0010t0001g0364 others(1): Show |
4 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+284C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418393 | |||||||
chr2:241418494 | GTC | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.771+389_771+390del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241418494 | ||||||
chr2:241418537 | T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.771+428T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418537 | |||||||
chr2:241418857 | C | T | 5 | a0001c0004t0001g0361 a0001c0004t0001g0362 a0001c0010t0001g0363 others(2): Show |
5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+748C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418857 | |||||||
chr2:241418865 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.771+756A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418865 | |||||||
chr2:241418884 | G | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.771+775G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418884 | |||||||
chr2:241419001 | A | G | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+892A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419001 | |||||||
chr2:241419069 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+960A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419069 | |||||||
chr2:241419204 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.771+1095G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419204 | |||||||
chr2:241419525 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+1416G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419525 | |||||||
chr2:241419544 | A | T | 1 | a0001c0004t0001g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.771+1435A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419544 | |||||||
chr2:241419662 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+1553A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419662 | |||||||
chr2:241419820 | T | A | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.771+1711T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419820 | |||||||
chr2:241419925 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.771+1816A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419925 | |||||||
chr2:241420168 | T | C | 1 | a0002c0002t0001g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.771+2059T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420168 | |||||||
chr2:241420237 | A | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+2128A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420237 | |||||||
chr2:241420244 | C | G | 2 | a0001c0003t0001g0020 a0001c0003t0001g0021 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.771+2135C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420244 | |||||||
chr2:241420404 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2295G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420404 | |||||||
chr2:241420490 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2381G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420490 | |||||||
chr2:241420605 | C | T | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.771+2496C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420605 | |||||||
chr2:241420670 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0004g0265 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.771+2561A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420670 | |||||||
chr2:241420686 | A | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.771+2577A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420686 | |||||||
chr2:241420830 | T | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0158 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.771+2721T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420830 | |||||||
chr2:241420895 | G | A | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.771+2786G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420895 | |||||||
chr2:241420919 | C | T | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.771+2810C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420919 | |||||||
chr2:241421203 | A | G | 5 | a0001c0004t0001g0361 a0001c0004t0001g0362 a0001c0010t0001g0363 others(2): Show |
5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+3094A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421203 | |||||||
chr2:241421281 | G | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3172G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421281 | |||||||
chr2:241421307 | C | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3198C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421307 | |||||||
chr2:241421309 | C | G | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.771+3200C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421309 | |||||||
chr2:241421504 | G | T | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.771+3395G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421504 | |||||||
chr2:241421552 | G | A | 1 | a0001c0001t0002g0375 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.771+3443G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421552 | |||||||
chr2:241421718 | GAT | G | 272 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.771+3613_771+3614d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241421718 | ||||||
chr2:241421721 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.771+3612A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421721 | |||||||
chr2:241421834 | G | A | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771+3725G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421834 | |||||||
chr2:241421883 | C | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.771+3774C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421883 | |||||||
chr2:241421915 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+3806G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421915 | |||||||
chr2:241422048 | A | G | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3939A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422048 | |||||||
chr2:241422131 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.771+4022C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422131 | |||||||
chr2:241422153 | C | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+4044C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422153 | |||||||
chr2:241422182 | G | A | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.771+4073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422182 | |||||||
chr2:241422200 | A | G | 285 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.771+4091A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422200 | |||||||
chr2:241422260 | C | CA | 11 | a0001c0001t0001g0128 a0001c0004t0001g0174 a0001c0004t0001g0370 others(8): Show |
11 | HG00323.hp1 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+4171dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | ||||||
chr2:241422260 | CA | C | 71 | a0001c0001t0001g0094 a0001c0001t0001g0205 a0001c0001t0001g0206 others(68): Show |
71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.771+4171delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | ||||||
chr2:241422260 | CAA | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0204 others(61): Show |
64 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.771+4170_771+4171d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | ||||||
chr2:241422312 | A | G | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.771+4203A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422312 | |||||||
chr2:241422402 | C | CA | 45 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(42): Show |
45 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.771+4304dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422402 | ||||||
chr2:241422413 | A | C | 3 | a0001c0001t0009g0106 a0001c0011t0001g0107 a0001c0011t0001g0108 |
3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.771+4304A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422413 | |||||||
chr2:241422474 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+4365C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422474 | |||||||
chr2:241422594 | G | A | 1 | a0003c0005t0001g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.771+4485G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422594 | |||||||
chr2:241422753 | C | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.771+4644C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422753 | |||||||
chr2:241422825 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.771+4716A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422825 | |||||||
chr2:241422846 | C | A | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.771+4737C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422846 | |||||||
chr2:241422894 | T | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+4785T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422894 | |||||||
chr2:241423261 | C | T | 1 | a0001c0003t0001g0026 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.771+5152C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423261 | |||||||
chr2:241423296 | G | A | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.771+5187G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423296 | |||||||
chr2:241423605 | A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771+5496A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423605 | |||||||
chr2:241423649 | T | G | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.771+5540T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423649 | |||||||
chr2:241423724 | C | T | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.771+5615C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423724 | |||||||
chr2:241423733 | A | G | 5 | a0005c0008t0001g0144 a0005c0008t0001g0148 a0005c0008t0001g0149 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+5624A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423733 | |||||||
chr2:241423911 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.771+5802T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423911 | |||||||
chr2:241423934 | A | G | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.771+5825A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423934 | |||||||
chr2:241424140 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.771+6031C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424140 | |||||||
chr2:241424149 | A | C | 285 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.771+6040A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424149 | |||||||
chr2:241424196 | G | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.771+6087G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424196 | |||||||
chr2:241424527 | A | G | 1 | a0020c0016t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.771+6418A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424527 | |||||||
chr2:241424692 | AAT | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.771+6585_771+6586d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241424692 | ||||||
chr2:241424704 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.771+6595G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424704 | |||||||
chr2:241424754 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.771+6645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424754 | |||||||
chr2:241424763 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.771+6654G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424763 | |||||||
chr2:241424783 | C | T | 1 | a0010c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.771+6674C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424783 | |||||||
chr2:241424814 | T | G | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.771+6705T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424814 | |||||||
chr2:241424880 | T | C | 285 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.771+6771T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424880 | |||||||
chr2:241425122 | G | A | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.772-6557G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425122 | |||||||
chr2:241425122 | G | T | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.772-6557G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425122 | |||||||
chr2:241425286 | C | T | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.772-6393C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425286 | |||||||
chr2:241425465 | G | A | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-6214G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425465 | |||||||
chr2:241425498 | T | C | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.772-6181T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425498 | |||||||
chr2:241425634 | T | TA | 58 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0081 others(55): Show |
58 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.772-6017dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | ||||||
chr2:241425634 | T | TAA | 10 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0025 others(7): Show |
10 | HG00280.hp1 HG00642.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-6018_772-6017d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | ||||||
chr2:241425634 | TA | T | 76 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0124 others(73): Show |
76 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.772-6017delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | ||||||
chr2:241425634 | TAA | T | 12 | a0001c0004t0001g0370 a0001c0006t0001g0236 a0001c0006t0001g0240 others(9): Show |
12 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.772-6018_772-6017d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | ||||||
chr2:241425688 | A | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772-5991A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425688 | |||||||
chr2:241425713 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.772-5966G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425713 | |||||||
chr2:241425741 | CT | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0142 others(207): Show |
210 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.772-5918delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425741 | ||||||
chr2:241425741 | CTT | C | 76 | a0001c0001t0001g0158 a0001c0001t0001g0206 a0001c0001t0001g0333 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.772-5919_772-5918d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425741 | ||||||
chr2:241425764 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0113 a0001c0001t0001g0131 others(2): Show |
5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-5915G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425764 | |||||||
chr2:241425863 | G | GT | 45 | a0001c0001t0001g0070 a0001c0001t0001g0205 a0001c0001t0001g0206 others(42): Show |
45 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.772-5803dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425863 | ||||||
chr2:241425863 | GT | G | 6 | a0001c0001t0001g0269 a0001c0003t0001g0053 a0001c0004t0001g0175 others(3): Show |
6 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-5803delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425863 | ||||||
chr2:241425864 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.772-5815T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425864 | |||||||
chr2:241425937 | TA | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-5739delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425937 | ||||||
chr2:241425938 | A | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-5741A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425938 | |||||||
chr2:241426228 | C | T | 2 | a0001c0001t0001g0158 a0001c0004t0001g0157 |
2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.772-5451C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426228 | |||||||
chr2:241426520 | G | A | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.772-5159G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426520 | |||||||
chr2:241426538 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-5141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426538 | |||||||
chr2:241426622 | G | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-5057G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426622 | |||||||
chr2:241426640 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-5039G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426640 | |||||||
chr2:241426645 | G | A | 1 | a0018c0018t0001g0338 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.772-5034G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426645 | |||||||
chr2:241426847 | C | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.772-4832C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426847 | |||||||
chr2:241426853 | A | G | 1 | a0002c0002t0001g0343 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.772-4826A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426853 | |||||||
chr2:241426960 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0201 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.772-4719C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426960 | |||||||
chr2:241426962 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-4717C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426962 | |||||||
chr2:241427085 | A | G | 34 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(31): Show |
34 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.772-4594A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427085 | |||||||
chr2:241427189 | C | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.772-4490C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427189 | |||||||
chr2:241427238 | A | AAC | 29 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(26): Show |
29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.772-4427_772-4426d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241427238 | ||||||
chr2:241427384 | C | T | 2 | a0002c0002t0001g0200 a0002c0002t0001g0358 |
2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.772-4295C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427384 | |||||||
chr2:241427449 | G | A | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.772-4230G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427449 | |||||||
chr2:241427693 | T | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.772-3986T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427693 | |||||||
chr2:241427714 | T | A | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-3965T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427714 | |||||||
chr2:241427765 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.772-3914G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427765 | |||||||
chr2:241427829 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.772-3850G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427829 | |||||||
chr2:241427955 | G | A | 4 | a0001c0001t0001g0378 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-3724G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427955 | |||||||
chr2:241427956 | C | T | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.772-3723C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427956 | |||||||
chr2:241427967 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.772-3712T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427967 | |||||||
chr2:241427987 | C | T | 340 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(337): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.772-3692C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427987 | |||||||
chr2:241428001 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772-3678C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428001 | |||||||
chr2:241428009 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3670G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428009 | |||||||
chr2:241428011 | C | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3668C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428011 | |||||||
chr2:241428040 | A | C | 2 | a0006c0009t0001g0183 a0006c0009t0001g0184 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.772-3639A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428040 | |||||||
chr2:241428045 | C | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-3634C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428045 | |||||||
chr2:241428046 | A | C | 26 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.772-3633A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428046 | |||||||
chr2:241428046 | A | G | 10 | a0001c0001t0001g0314 a0001c0004t0001g0359 a0001c0004t0001g0360 others(7): Show |
10 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-3633A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428046 | |||||||
chr2:241428056 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3623A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428056 | |||||||
chr2:241428058 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3621G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428058 | |||||||
chr2:241428062 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3617A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428062 | |||||||
chr2:241428074 | C | T | 29 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.772-3605C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428074 | |||||||
chr2:241428202 | G | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.772-3477G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428202 | |||||||
chr2:241428217 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.772-3462A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428217 | |||||||
chr2:241428234 | C | CT | 225 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0158 others(222): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.772-3427dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428234 | ||||||
chr2:241428234 | C | CTT | 11 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0001g0238 others(8): Show |
11 | HG00639.hp1 HG01358.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-3428_772-3427d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428234 | ||||||
chr2:241428261 | G | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-3418G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428261 | |||||||
chr2:241428282 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0262 others(5): Show |
8 | HG02257.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-3397T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428282 | |||||||
chr2:241428294 | G | A | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.772-3385G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428294 | |||||||
chr2:241428298 | AG | A | 5 | a0006c0009t0001g0183 a0006c0009t0001g0184 a0006c0009t0001g0185 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-3380delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428298 | |||||||
chr2:241428401 | AT | A | 34 | a0001c0001t0001g0080 a0001c0001t0001g0205 a0001c0001t0001g0206 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.772-3263delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428401 | ||||||
chr2:241428440 | C | T | 2 | a0003c0005t0001g0198 a0003c0005t0001g0199 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.772-3239C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428440 | |||||||
chr2:241428451 | C | T | 1 | a0010c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.772-3228C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428451 | |||||||
chr2:241428461 | G | A | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-3218G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428461 | |||||||
chr2:241428498 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | NA18953.hp1 NA19000.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-3181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428498 | |||||||
chr2:241428500 | A | G | 29 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(26): Show |
29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.772-3179A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428500 | |||||||
chr2:241428536 | G | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3143G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428536 | |||||||
chr2:241428590 | GT | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-3086delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428590 | ||||||
chr2:241428625 | AT | A | 7 | a0001c0001t0001g0142 a0001c0001t0001g0378 a0001c0004t0001g0143 others(4): Show |
7 | HG00408.hp1 HG01358.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-3041delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428625 | ||||||
chr2:241428655 | G | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.772-3024G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428655 | |||||||
chr2:241428675 | T | C | 2 | a0001c0003t0001g0060 a0001c0003t0008g0061 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.772-3004T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428675 | |||||||
chr2:241428689 | A | G | 11 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2990A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428689 | |||||||
chr2:241428726 | C | T | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-2953C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428726 | |||||||
chr2:241428800 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-2879G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428800 | |||||||
chr2:241428910 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-2769C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428910 | |||||||
chr2:241428993 | G | A | 6 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0003c0005t0001g0049 others(3): Show |
6 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-2686G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428993 | |||||||
chr2:241429278 | A | G | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.772-2401A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429278 | |||||||
chr2:241429310 | G | A | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-2369G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429310 | |||||||
chr2:241429352 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.772-2327C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429352 | |||||||
chr2:241429443 | G | T | 1 | a0003c0005t0001g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.772-2236G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429443 | |||||||
chr2:241429632 | A | G | 32 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(29): Show |
32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.772-2047A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429632 | |||||||
chr2:241429656 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-2023G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429656 | |||||||
chr2:241429709 | C | A | 6 | a0001c0003t0001g0028 a0001c0003t0001g0034 a0001c0003t0001g0035 others(3): Show |
6 | HG02132.hp2 NA18972.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-1970C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429709 | |||||||
chr2:241429868 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-1811A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429868 | |||||||
chr2:241430270 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-1409A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430270 | |||||||
chr2:241430450 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.772-1229C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430450 | |||||||
chr2:241430482 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.772-1197A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430482 | |||||||
chr2:241430733 | A | C | 3 | a0001c0001t0001g0378 a0009c0012t0001g0001 a0009c0012t0001g0002 |
3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-946A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430733 | |||||||
chr2:241430868 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.772-811C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430868 | |||||||
chr2:241430952 | A | T | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.772-727A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430952 | |||||||
chr2:241430999 | C | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-680C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430999 | |||||||
chr2:241431004 | A | G | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-675A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431004 | |||||||
chr2:241431083 | A | T | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.772-596A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431083 | |||||||
chr2:241431148 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | NA18943.hp2 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.772-531A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431148 | |||||||
chr2:241431158 | A | T | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.772-521A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431158 | |||||||
chr2:241431196 | G | C | 1 | a0003c0005t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.772-483G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431196 | |||||||
chr2:241431248 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.772-431A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431248 | |||||||
chr2:241431303 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.772-376C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431303 | |||||||
chr2:241431336 | G | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(172): Show |
175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.772-343G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431336 | |||||||
chr2:241431372 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG00733.hp1 HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.772-307G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431372 | |||||||
chr2:241431540 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.772-139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431540 | |||||||
chr2:241431810 | T | TTTTA | 3 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0001c0003t0001g0053 |
3 | HG01167.hp1 HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.867+56_867+59dupAT others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241431810 | ||||||
chr2:241431826 | A | T | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+52A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431826 | |||||||
chr2:241431830 | A | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0272 a0001c0001t0001g0304 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+56A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431830 | |||||||
chr2:241431842 | C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.867+68C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431842 | |||||||
chr2:241431923 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.867+149G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431923 | |||||||
chr2:241432053 | T | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.867+279T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432053 | |||||||
chr2:241432282 | G | C | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.867+508G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432282 | |||||||
chr2:241432410 | G | A | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.867+636G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432410 | |||||||
chr2:241432596 | G | A | 1 | a0001c0003t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.867+822G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432596 | |||||||
chr2:241432688 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+914A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432688 | |||||||
chr2:241432689 | T | G | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+915T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432689 | |||||||
chr2:241432691 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+917G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432691 | |||||||
chr2:241432880 | A | T | 5 | a0005c0008t0001g0144 a0005c0008t0001g0148 a0005c0008t0001g0149 others(2): Show |
5 | HG02647.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+1106A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432880 | |||||||
chr2:241432953 | A | G | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.867+1179A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432953 | |||||||
chr2:241433011 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.868-1147G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433011 | |||||||
chr2:241433059 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.868-1099A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433059 | |||||||
chr2:241433095 | C | T | 5 | a0005c0008t0001g0146 a0005c0008t0001g0147 a0005c0008t0001g0151 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-1063C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433095 | |||||||
chr2:241433104 | A | G | 3 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.868-1054A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433104 | |||||||
chr2:241433129 | T | TA | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.868-1016dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241433129 | ||||||
chr2:241433155 | T | A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.868-1003T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433155 | |||||||
chr2:241433160 | G | A | 1 | a0002c0002t0001g0347 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.868-998G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433160 | |||||||
chr2:241433316 | T | C | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.868-842T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433316 | |||||||
chr2:241433503 | TATACC | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.868-652_868-648del others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241433503 | ||||||
chr2:241434090 | C | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.868-68C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434090 | |||||||
chr2:241434096 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.868-62T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434096 | |||||||
chr2:241434145 | G | A | 1 | a0017c0026t0001g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.868-13G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434145 | |||||||
chr2:241434335 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1031+14C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434335 | |||||||
chr2:241434566 | T | A | 1 | a0001c0001t0001g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1031+245T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434566 | |||||||
chr2:241434744 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1032-218C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434744 | |||||||
chr2:241434763 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1032-199A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434763 | |||||||
chr2:241434792 | C | T | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1032-170C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434792 | |||||||
chr2:241434800 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1032-162C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434800 | |||||||
chr2:241434823 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1032-139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434823 | |||||||
chr2:241434833 | C | G | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1032-129C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434833 | |||||||
chr2:241434918 | C | G | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1032-44C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434918 | |||||||
chr2:241434943 | T | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1032-19T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434943 | |||||||
chr2:241435038 | C | T | 2 | a0003c0005t0001g0045 a0003c0005t0001g0048 |
2 | HG02055.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1100+8C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435038 | |||||||
chr2:241435104 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1100+74C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435104 | |||||||
chr2:241435130 | G | A | 1 | a0016c0027t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1100+100G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435130 | |||||||
chr2:241435162 | C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1100+132C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435162 | |||||||
chr2:241435198 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1100+168A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435198 | |||||||
chr2:241435218 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1100+188C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435218 | |||||||
chr2:241435243 | A | G | 1 | a0005c0014t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1100+213A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435243 | |||||||
chr2:241435261 | G | GT | 10 | a0002c0002t0001g0344 a0002c0002t0001g0345 a0002c0002t0001g0346 others(7): Show |
10 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+239dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435261 | ||||||
chr2:241435270 | G | GT | 16 | a0001c0001t0001g0080 a0001c0001t0001g0206 a0001c0001t0001g0219 others(13): Show |
16 | HG00642.hp1 HG02056.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1100+254dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435270 | ||||||
chr2:241435294 | C | T | 2 | a0003c0005t0001g0045 a0003c0005t0001g0048 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1100+264C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435294 | |||||||
chr2:241435342 | G | GT | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1100+313dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435342 | ||||||
chr2:241435376 | G | A | 1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1100+346G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435376 | |||||||
chr2:241435452 | A | G | 3 | a0001c0001t0009g0106 a0001c0011t0001g0107 a0001c0011t0001g0108 |
3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1100+422A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435452 | |||||||
chr2:241435510 | A | AT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0201 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1100+499dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435510 | ||||||
chr2:241435593 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1100+563G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435593 | |||||||
chr2:241435598 | G | A | 33 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(30): Show |
33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1100+568G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435598 | |||||||
chr2:241435757 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1101-724C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435757 | |||||||
chr2:241435758 | G | A | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1101-723G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435758 | |||||||
chr2:241435833 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1101-648T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435833 | |||||||
chr2:241435908 | A | AT | 87 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0201 others(84): Show |
87 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1101-551dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | ||||||
chr2:241435908 | A | ATT | 8 | a0001c0001t0001g0270 a0001c0001t0001g0286 a0001c0001t0001g0289 others(5): Show |
8 | HG02135.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1101-552_1101-551d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | ||||||
chr2:241435908 | AT | A | 76 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0112 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1101-551delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | ||||||
chr2:241436014 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1101-467G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436014 | |||||||
chr2:241436248 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1101-233C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436248 | |||||||
chr2:241436398 | A | T | 30 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(27): Show |
30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1101-83A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436398 | |||||||
chr2:241436637 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158+99A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436637 | |||||||
chr2:241436771 | G | T | 39 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(36): Show |
39 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1158+233G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436771 | |||||||
chr2:241436861 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1158+323G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436861 | |||||||
chr2:241436918 | T | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1158+380T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436918 | |||||||
chr2:241436987 | A | G | 4 | a0002c0002t0001g0256 a0002c0002t0001g0260 a0002c0002t0001g0261 others(1): Show |
4 | HG00639.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158+449A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436987 | |||||||
chr2:241437084 | TACTA | T | 44 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1158+551_1158+554d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437084 | ||||||
chr2:241437092 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1158+554A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437092 | |||||||
chr2:241437190 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1158+652T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437190 | |||||||
chr2:241437259 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1158+721A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437259 | |||||||
chr2:241437260 | C | G | 1 | a0005c0008t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1158+722C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437260 | |||||||
chr2:241437276 | C | T | 5 | a0001c0004t0001g0178 a0001c0004t0001g0179 a0001c0004t0001g0180 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158+738C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437276 | |||||||
chr2:241437364 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1158+826G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437364 | |||||||
chr2:241437522 | G | C | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158+984G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437522 | |||||||
chr2:241437576 | AT | A | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1040delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437576 | ||||||
chr2:241437580 | C | G | 15 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(12): Show |
15 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1158+1042C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437580 | |||||||
chr2:241437648 | A | ATATTTAT others(1): Show |
85 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1158+1128_1158+113 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437648 | ||||||
chr2:241437648 | A | ATATTTAT others(5): Show |
3 | a0001c0001t0001g0296 a0001c0001t0001g0310 a0001c0001t0001g0333 |
3 | HG00735.hp2 HG03017.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1158+1124_1158+113 others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437648 | ||||||
chr2:241437648 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1158+1110A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437648 | |||||||
chr2:241437652 | T | A | 38 | a0001c0001t0009g0106 a0001c0011t0001g0107 a0001c0011t0001g0108 others(35): Show |
38 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1158+1114T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437652 | |||||||
chr2:241437658 | A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0343 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1158+1123_1158+112 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437658 | ||||||
chr2:241437662 | A | ATTTTTTT others(2): Show |
17 | a0002c0002t0001g0200 a0002c0002t0001g0258 a0002c0002t0001g0335 others(14): Show |
17 | HG00735.hp1 HG01081.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.1158+1127_1158+112 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437662 | ||||||
chr2:241437662 | A | ATTTTTTT others(3): Show |
2 | a0002c0002t0001g0347 a0002c0002t0001g0358 |
2 | HG01433.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1158+1127_1158+112 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437662 | ||||||
chr2:241437662 | A | T | 6 | a0001c0015t0002g0371 a0002c0002t0001g0257 a0002c0002t0001g0259 others(3): Show |
6 | HG00609.hp2 HG01256.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+1124A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437662 | |||||||
chr2:241437664 | T | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1158+1126T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437664 | |||||||
chr2:241437666 | A | AT | 20 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(17): Show |
20 | HG00140.hp1 HG00423.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1158+1131dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437666 | ||||||
chr2:241437666 | A | ATTTTTTT others(2): Show |
6 | a0001c0001t0001g0206 a0002c0002t0001g0253 a0002c0002t0001g0254 others(3): Show |
6 | HG00597.hp1 HG00738.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+1131_1158+113 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437666 | ||||||
chr2:241437666 | A | T | 39 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0215 others(36): Show |
39 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1158+1128A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437666 | |||||||
chr2:241437670 | A | AT | 10 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(7): Show |
10 | HG00280.hp2 HG00323.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1158+1144dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | ||||||
chr2:241437670 | A | ATTTATTT others(2): Show |
6 | a0001c0006t0001g0244 a0001c0006t0001g0245 a0001c0006t0001g0246 others(3): Show |
6 | HG00408.hp1 HG00597.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+1135_1158+113 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | ||||||
chr2:241437670 | A | ATTTATTT others(1): Show |
6 | a0001c0001t0001g0209 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG01358.hp1 HG02027.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+1135_1158+113 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | ||||||
chr2:241437670 | A | ATTTTTTT others(1): Show |
14 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(11): Show |
14 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1158+1137_1158+114 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | ||||||
chr2:241437670 | A | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0063 a0001c0001t0001g0064 others(105): Show |
108 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1158+1132A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437670 | |||||||
chr2:241437674 | T | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1158+1136T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437674 | |||||||
chr2:241437677 | T | A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1158+1139T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437677 | |||||||
chr2:241437759 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1158+1221T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437759 | |||||||
chr2:241437809 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1158+1271T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437809 | |||||||
chr2:241437825 | T | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1158+1287T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437825 | |||||||
chr2:241437856 | G | A | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158+1318G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437856 | |||||||
chr2:241437862 | T | C | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158+1324T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437862 | |||||||
chr2:241437911 | C | T | 1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1158+1373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437911 | |||||||
chr2:241437916 | C | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1378C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437916 | |||||||
chr2:241437941 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1158+1403A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437941 | |||||||
chr2:241437963 | C | G | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1158+1425C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437963 | |||||||
chr2:241437964 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1158+1426C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437964 | |||||||
chr2:241438079 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1158+1541G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438079 | |||||||
chr2:241438260 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1158+1722T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438260 | |||||||
chr2:241438267 | C | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1158+1729C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438267 | |||||||
chr2:241438284 | A | G | 285 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1158+1746A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438284 | |||||||
chr2:241438371 | A | G | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1833A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438371 | |||||||
chr2:241438405 | A | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1158+1867A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438405 | |||||||
chr2:241438486 | G | A | 1 | a0007c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1158+1948G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438486 | |||||||
chr2:241438547 | A | C | 5 | a0001c0004t0001g0361 a0001c0004t0001g0362 a0001c0010t0001g0363 others(2): Show |
5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158+2009A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438547 | |||||||
chr2:241438581 | G | T | 285 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1158+2043G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438581 | |||||||
chr2:241438585 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1158+2047T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438585 | |||||||
chr2:241438621 | G | GT | 78 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(75): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1158+2095dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241438621 | ||||||
chr2:241438634 | G | GT | 17 | a0001c0001t0001g0083 a0001c0001t0001g0138 a0001c0001t0001g0298 others(14): Show |
17 | HG00140.hp1 HG02451.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1158+2109dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241438634 | ||||||
chr2:241438634 | G | T | 4 | a0001c0001t0001g0378 a0002c0002t0001g0354 a0009c0012t0001g0001 others(1): Show |
4 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158+2096G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438634 | |||||||
chr2:241438638 | T | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1158+2100T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438638 | |||||||
chr2:241438642 | T | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1158+2104T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438642 | |||||||
chr2:241438660 | C | T | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1158+2122C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438660 | |||||||
chr2:241438661 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1158+2123G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438661 | |||||||
chr2:241438693 | G | A | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1158+2155G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438693 | |||||||
chr2:241438723 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1158+2185G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438723 | |||||||
chr2:241438933 | C | T | 25 | a0002c0002t0001g0200 a0002c0002t0001g0335 a0002c0002t0001g0336 others(22): Show |
25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1159-2371C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438933 | |||||||
chr2:241439169 | C | G | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1159-2135C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439169 | |||||||
chr2:241439178 | G | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1159-2126G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439178 | |||||||
chr2:241439179 | C | T | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1159-2125C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439179 | |||||||
chr2:241439339 | C | A | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1159-1965C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439339 | |||||||
chr2:241439490 | T | C | 31 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(28): Show |
31 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1159-1814T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439490 | |||||||
chr2:241439531 | G | A | 1 | a0001c0004t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1159-1773G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439531 | |||||||
chr2:241439571 | C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1159-1733C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439571 | |||||||
chr2:241439625 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(4): Show |
7 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159-1679G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439625 | |||||||
chr2:241439732 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1159-1572C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439732 | |||||||
chr2:241439831 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1159-1473G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439831 | |||||||
chr2:241439833 | G | C | 372 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(369): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1159-1471G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439833 | |||||||
chr2:241440222 | G | A | 9 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159-1082G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440222 | |||||||
chr2:241440278 | G | A | 3 | a0001c0010t0001g0363 a0001c0010t0001g0364 a0001c0010t0001g0365 |
3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1159-1026G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440278 | |||||||
chr2:241440336 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1159-968G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440336 | |||||||
chr2:241440371 | C | T | 1 | a0007c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159-933C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440371 | |||||||
chr2:241440380 | G | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(86): Show |
89 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1159-924G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440380 | |||||||
chr2:241440512 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1159-792A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440512 | |||||||
chr2:241440967 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1159-337T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440967 | |||||||
chr2:241441021 | TG | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1159-282delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241441021 | |||||||
chr2:241441057 | T | C | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1159-247T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241441057 | |||||||
chr2:241441074 | G | GA | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1159-223dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241441074 | ||||||
chr2:241441561 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.1411+5C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241441561 | |||||||
chr2:241441733 | C | T | 2 | a0002c0002t0001g0200 a0002c0002t0001g0358 |
2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1411+177C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241441733 | |||||||
chr2:241442142 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1411+586T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442142 | |||||||
chr2:241442718 | C | T | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+1162C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442718 | |||||||
chr2:241442732 | C | G | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411+1176C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442732 | |||||||
chr2:241442735 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+1179C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442735 | |||||||
chr2:241442777 | C | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1411+1221C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442777 | |||||||
chr2:241442816 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1411+1260G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442816 | |||||||
chr2:241442886 | A | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+1330A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442886 | |||||||
chr2:241443104 | C | T | 1 | a0001c0003t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1411+1548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443104 | |||||||
chr2:241443191 | A | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1411+1635A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443191 | |||||||
chr2:241443242 | A | G | 1 | a0001c0003t0001g0007 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1411+1686A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443242 | |||||||
chr2:241443291 | A | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1411+1735A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443291 | |||||||
chr2:241443301 | T | C | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1411+1745T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443301 | |||||||
chr2:241443449 | C | T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1411+1893C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443449 | |||||||
chr2:241443563 | G | A | 1 | a0002c0002t0001g0341 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1411+2007G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443563 | |||||||
chr2:241443671 | A | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1411+2115A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443671 | |||||||
chr2:241443703 | G | GCC | 4 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(1): Show |
4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+2148_1411+214 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241443703 | ||||||
chr2:241443875 | A | C | 11 | a0004c0007t0001g0096 a0004c0007t0001g0097 a0004c0007t0001g0100 others(8): Show |
11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+2319A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443875 | |||||||
chr2:241443985 | C | G | 4 | a0003c0005t0001g0192 a0003c0005t0001g0198 a0003c0005t0001g0199 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2429C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443985 | |||||||
chr2:241444080 | G | A | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+2524G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444080 | |||||||
chr2:241444134 | T | C | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1411+2578T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444134 | |||||||
chr2:241444168 | TTGA | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1411+2615_1411+261 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241444168 | ||||||
chr2:241444332 | G | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+2776G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444332 | |||||||
chr2:241444513 | G | T | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1411+2957G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444513 | |||||||
chr2:241444639 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+3083A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444639 | |||||||
chr2:241444660 | G | A | 1 | a0015c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1411+3104G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444660 | |||||||
chr2:241444696 | G | A | 3 | a0005c0008t0001g0147 a0005c0008t0001g0151 a0005c0014t0001g0150 |
3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1411+3140G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444696 | |||||||
chr2:241444732 | G | T | 7 | a0001c0004t0001g0359 a0001c0004t0001g0360 a0001c0004t0001g0361 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+3176G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444732 | |||||||
chr2:241444779 | C | G | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1411+3223C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444779 | |||||||
chr2:241444893 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3337T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444893 | |||||||
chr2:241444899 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3343C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444899 | |||||||
chr2:241444900 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3344T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444900 | |||||||
chr2:241444953 | G | A | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1411+3397G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444953 | |||||||
chr2:241444983 | A | C | 1 | a0005c0008t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1411+3427A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444983 | |||||||
chr2:241445043 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1411+3487C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445043 | |||||||
chr2:241445087 | G | A | 1 | a0005c0008t0001g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1411+3531G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445087 | |||||||
chr2:241445160 | G | A | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1411+3604G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445160 | |||||||
chr2:241445166 | C | A | 273 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0201 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1411+3610C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445166 | |||||||
chr2:241445166 | C | G | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+3610C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445166 | |||||||
chr2:241445212 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+3656A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445212 | |||||||
chr2:241445244 | C | CA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 others(121): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1411+3708dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | ||||||
chr2:241445244 | C | CAA | 128 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0069 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1411+3707_1411+370 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | ||||||
chr2:241445244 | C | CAAA | 11 | a0001c0001t0001g0103 a0001c0001t0001g0269 a0001c0001t0001g0286 others(8): Show |
11 | HG01934.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+3706_1411+370 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | ||||||
chr2:241445320 | G | T | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+3764G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445320 | |||||||
chr2:241445377 | G | T | 1 | a0001c0003t0008g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1411+3821G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445377 | |||||||
chr2:241445380 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+3824G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445380 | |||||||
chr2:241445428 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1411+3872C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445428 | |||||||
chr2:241445561 | T | C | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+4005T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445561 | |||||||
chr2:241445851 | A | C | 11 | a0004c0007t0001g0096 a0004c0007t0001g0097 a0004c0007t0001g0100 others(8): Show |
11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+4295A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445851 | |||||||
chr2:241445925 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(86): Show |
89 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1411+4369A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445925 | |||||||
chr2:241446497 | G | GGAGTAAT others(6): Show |
1 | a0004c0007t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1411+4942_1411+495 others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241446497 | ||||||
chr2:241446600 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5044A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446600 | |||||||
chr2:241446601 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5045A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446601 | |||||||
chr2:241446640 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+5084C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446640 | |||||||
chr2:241446685 | A | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5129A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446685 | |||||||
chr2:241446738 | T | TC | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411+5182_1411+518 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446738 | |||||||
chr2:241446765 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1411+5209T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446765 | |||||||
chr2:241447167 | T | C | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411+5611T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447167 | |||||||
chr2:241447239 | A | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+5683A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447239 | |||||||
chr2:241447455 | C | T | 30 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1411+5899C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447455 | |||||||
chr2:241447464 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+5908C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447464 | |||||||
chr2:241447931 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1411+6375G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447931 | |||||||
chr2:241448283 | A | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+6727A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448283 | |||||||
chr2:241448371 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0224 |
2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1411+6815A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448371 | |||||||
chr2:241448407 | G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1411+6851G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448407 | |||||||
chr2:241448527 | A | G | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+6971A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448527 | |||||||
chr2:241448569 | A | G | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+7013A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448569 | |||||||
chr2:241448599 | A | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1411+7043A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448599 | |||||||
chr2:241448756 | C | A | 1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1411+7200C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448756 | |||||||
chr2:241448810 | G | T | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+7254G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448810 | |||||||
chr2:241449015 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0086 |
3 | NA18961.hp2 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1411+7459G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449015 | |||||||
chr2:241449048 | T | G | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1411+7492T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449048 | |||||||
chr2:241449094 | C | T | 3 | a0001c0001t0002g0372 a0001c0001t0002g0374 a0001c0015t0002g0371 |
3 | HG01261.hp2 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1411+7538C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449094 | |||||||
chr2:241449135 | T | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0158 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1411+7579T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449135 | |||||||
chr2:241449270 | G | A | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1412-7477G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449270 | |||||||
chr2:241449375 | G | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0158 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1412-7372G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449375 | |||||||
chr2:241449388 | A | G | 2 | a0001c0001t0001g0142 a0001c0004t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1412-7359A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449388 | |||||||
chr2:241449412 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1412-7335G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449412 | |||||||
chr2:241449515 | CTT | C | 31 | a0001c0001t0001g0158 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-7230_1412-722 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241449515 | ||||||
chr2:241449694 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1412-7053G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449694 | |||||||
chr2:241449725 | G | A | 1 | a0005c0008t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1412-7022G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449725 | |||||||
chr2:241449766 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1412-6981A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449766 | |||||||
chr2:241449811 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0001c0001t0001g0202 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1412-6936A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449811 | |||||||
chr2:241449867 | C | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1412-6880C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449867 | |||||||
chr2:241449876 | G | A | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-6871G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449876 | |||||||
chr2:241449880 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1412-6867G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449880 | |||||||
chr2:241449942 | G | A | 1 | a0002c0002t0001g0337 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1412-6805G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449942 | |||||||
chr2:241450101 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1412-6646G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450101 | |||||||
chr2:241450312 | A | G | 10 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0147 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-6435A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450312 | |||||||
chr2:241450415 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1412-6332C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450415 | |||||||
chr2:241450450 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-6297G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450450 | |||||||
chr2:241450450 | G | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0136 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1412-6297G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450450 | |||||||
chr2:241450557 | TCAGGAGG others(1244): Show |
T | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1412-6186_1412-493 others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241450557 | ||||||
chr2:241450591 | A | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-6156A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450591 | |||||||
chr2:241450640 | C | T | 1 | a0001c0006t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1412-6107C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450640 | |||||||
chr2:241450995 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1412-5752T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450995 | |||||||
chr2:241451066 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-5681C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451066 | |||||||
chr2:241451081 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1412-5666T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451081 | |||||||
chr2:241451111 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18966.hp2 NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1412-5636C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451111 | |||||||
chr2:241451554 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-5193T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451554 | |||||||
chr2:241451647 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
4 | HG01070.hp2 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-5100G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451647 | |||||||
chr2:241451660 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1412-5087A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451660 | |||||||
chr2:241451676 | T | C | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1412-5071T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451676 | |||||||
chr2:241451741 | T | G | 5 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | NA18953.hp1 NA19000.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-5006T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451741 | |||||||
chr2:241451752 | T | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-4995T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451752 | |||||||
chr2:241451762 | T | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1412-4985T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451762 | |||||||
chr2:241451768 | T | G | 57 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(54): Show |
57 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1412-4979T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451768 | |||||||
chr2:241451797 | C | T | 57 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(54): Show |
57 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1412-4950C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451797 | |||||||
chr2:241451817 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-4930C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451817 | |||||||
chr2:241451818 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1412-4929G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451818 | |||||||
chr2:241451885 | G | A | 5 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(2): Show |
5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-4862G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451885 | |||||||
chr2:241451994 | A | C | 18 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(15): Show |
18 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-4753A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451994 | |||||||
chr2:241452203 | A | G | 1 | a0001c0004t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1412-4544A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452203 | |||||||
chr2:241452287 | C | T | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1412-4460C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452287 | |||||||
chr2:241452425 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1412-4322A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452425 | |||||||
chr2:241452643 | A | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-4104A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452643 | |||||||
chr2:241452815 | T | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0158 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1412-3932T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452815 | |||||||
chr2:241452848 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1412-3899C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452848 | |||||||
chr2:241452937 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1412-3810G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452937 | |||||||
chr2:241452942 | CA | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01167.hp1 HG01168.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-3793delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241452942 | ||||||
chr2:241453052 | C | T | 1 | a0005c0008t0001g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1412-3695C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453052 | |||||||
chr2:241453058 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3689G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453058 | |||||||
chr2:241453099 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3648G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453099 | |||||||
chr2:241453135 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1412-3612A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453135 | |||||||
chr2:241453139 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1412-3608G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453139 | |||||||
chr2:241453236 | A | G | 42 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0237 others(39): Show |
42 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-3511A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453236 | |||||||
chr2:241453278 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1412-3469C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453278 | |||||||
chr2:241453312 | A | G | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1412-3435A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453312 | |||||||
chr2:241453344 | T | C | 28 | a0001c0001t0001g0142 a0001c0003t0001g0054 a0001c0003t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00642.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.1412-3403T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453344 | |||||||
chr2:241453360 | T | C | 123 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(120): Show |
123 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1412-3387T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453360 | |||||||
chr2:241453388 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3359C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453388 | |||||||
chr2:241453389 | A | G | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3358A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453389 | |||||||
chr2:241453393 | C | T | 5 | a0001c0001t0001g0309 a0001c0001t0001g0315 a0001c0001t0001g0316 others(2): Show |
5 | HG02132.hp1 HG02135.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-3354C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453393 | |||||||
chr2:241453397 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3350C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453397 | |||||||
chr2:241453398 | A | G | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3349A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453398 | |||||||
chr2:241453418 | C | A | 2 | a0001c0004t0001g0164 a0003c0005t0001g0369 |
2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-3329C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453418 | |||||||
chr2:241453418 | C | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1412-3329C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453418 | |||||||
chr2:241453426 | T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1412-3321T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453426 | |||||||
chr2:241453433 | T | C | 33 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1412-3314T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453433 | |||||||
chr2:241453438 | T | C | 96 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1412-3309T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453438 | |||||||
chr2:241453439 | G | A | 40 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0325 others(37): Show |
40 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1412-3308G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453439 | |||||||
chr2:241453443 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1412-3304A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453443 | |||||||
chr2:241453447 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0327 |
3 | HG01928.hp2 HG01975.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1412-3300C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453447 | |||||||
chr2:241453449 | C | T | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1412-3298C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453449 | |||||||
chr2:241453450 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1412-3297G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453450 | |||||||
chr2:241453451 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0280 |
3 | HG01928.hp2 HG01975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1412-3296T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453451 | |||||||
chr2:241453494 | A | C | 4 | a0001c0001t0001g0271 a0001c0006t0001g0246 a0009c0012t0001g0001 others(1): Show |
4 | HG02630.hp2 HG02698.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-3253A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453494 | |||||||
chr2:241453539 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3208A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453539 | |||||||
chr2:241453546 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3201T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453546 | |||||||
chr2:241453553 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3194C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453553 | |||||||
chr2:241453603 | A | C | 3 | a0007c0021t0003g0334 a0009c0012t0001g0001 a0009c0012t0001g0002 |
3 | HG00140.hp2 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1412-3144A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453603 | |||||||
chr2:241453609 | G | A | 1 | a0007c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1412-3138G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453609 | |||||||
chr2:241453621 | C | CA | 32 | a0001c0001t0001g0228 a0001c0003t0001g0007 a0001c0003t0001g0008 others(29): Show |
32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1412-3113dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453621 | ||||||
chr2:241453672 | C | T | 20 | a0001c0001t0001g0158 a0001c0004t0001g0143 a0001c0004t0001g0157 others(17): Show |
20 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1412-3075C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453672 | |||||||
chr2:241453768 | GGTT | G | 17 | a0001c0004t0001g0370 a0001c0006t0001g0240 a0001c0006t0001g0241 others(14): Show |
17 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | |||||||
chr2:241453768 | GGTTT | G | 35 | a0001c0004t0001g0359 a0001c0006t0001g0236 a0001c0006t0001g0242 others(32): Show |
35 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | |||||||
chr2:241453768 | GGTTTT | G | 21 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | |||||||
chr2:241453768 | GGTTTTT | G | 42 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(39): Show |
42 | HG00423.hp2 HG00639.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | |||||||
chr2:241453768 | GGTTTTTT | G | 46 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0012 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | |||||||
chr2:241453769 | G | GT | 17 | a0001c0001t0001g0093 a0001c0001t0001g0104 a0001c0001t0001g0110 others(14): Show |
17 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1412-2946dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453769 | G | GTT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0378 a0001c0001t0002g0372 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-2947_1412-294 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453769 | G | GTTTTT | 11 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG00280.hp2 HG00323.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2950_1412-294 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453769 | G | GTTTTTT | 16 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0070 others(13): Show |
16 | HG00423.hp1 HG01934.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-2951_1412-294 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453769 | GTT | G | 33 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0001t0001g0262 others(30): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1412-2947_1412-294 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453769 | GTTT | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0158 others(79): Show |
82 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1412-2948_1412-294 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | ||||||
chr2:241453775 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1412-2972T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453775 | |||||||
chr2:241453780 | T | G | 1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1412-2967T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453780 | |||||||
chr2:241453848 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-2899A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453848 | |||||||
chr2:241453885 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18966.hp2 NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1412-2862G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453885 | |||||||
chr2:241453958 | AT | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0142 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1412-2782delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453958 | ||||||
chr2:241454081 | G | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0377 |
2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1412-2666G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454081 | |||||||
chr2:241454159 | T | A | 244 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0142 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-2588T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454159 | |||||||
chr2:241454212 | C | T | 5 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0003c0005t0001g0049 others(2): Show |
5 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-2535C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454212 | |||||||
chr2:241454243 | A | C | 49 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(46): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1412-2504A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454243 | |||||||
chr2:241454380 | G | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(198): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1412-2367G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454380 | |||||||
chr2:241454383 | A | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(119): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1412-2364A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454383 | |||||||
chr2:241454455 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0113 a0001c0001t0001g0131 others(2): Show |
5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-2292G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454455 | |||||||
chr2:241454468 | A | G | 10 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-2279A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454468 | |||||||
chr2:241454588 | T | C | 32 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1412-2159T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454588 | |||||||
chr2:241454726 | G | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0142 others(190): Show |
193 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1412-2021G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454726 | |||||||
chr2:241454727 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1412-2020G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454727 | |||||||
chr2:241454807 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1412-1940A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454807 | |||||||
chr2:241454971 | C | T | 1 | a0001c0022t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-1776C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454971 | |||||||
chr2:241454973 | C | G | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1412-1774C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454973 | |||||||
chr2:241455150 | A | G | 1 | a0001c0006t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1412-1597A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455150 | |||||||
chr2:241455309 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-1438A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455309 | |||||||
chr2:241455452 | C | T | 1 | a0003c0005t0001g0057 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1412-1295C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455452 | |||||||
chr2:241455541 | C | T | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-1206C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455541 | |||||||
chr2:241455735 | C | CT | 74 | a0001c0001t0001g0095 a0001c0001t0001g0113 a0001c0001t0001g0220 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1412-990dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | ||||||
chr2:241455735 | C | CTT | 30 | a0001c0003t0001g0024 a0001c0003t0001g0033 a0001c0003t0007g0037 others(27): Show |
30 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1412-991_1412-990d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | ||||||
chr2:241455735 | CT | C | 72 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1412-990delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | ||||||
chr2:241455735 | CTTTTTTT | C | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-996_1412-990d others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | ||||||
chr2:241455900 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(88): Show |
91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1412-847C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455900 | |||||||
chr2:241455940 | C | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1412-807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455940 | |||||||
chr2:241455999 | T | TAGAAAAA others(1578): Show |
2 | a0006c0009t0001g0183 a0006c0009t0001g0184 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1412-729_1412-728i others(1587): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455999 | ||||||
chr2:241456108 | A | C | 1 | a0001c0001t0001g0294 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-639A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456108 | |||||||
chr2:241456139 | A | G | 70 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(67): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1412-608A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456139 | |||||||
chr2:241456171 | T | G | 36 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0004t0001g0143 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1412-576T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456171 | |||||||
chr2:241456259 | G | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0142 others(210): Show |
213 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1412-488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456259 | |||||||
chr2:241456376 | G | A | 2 | a0001c0004t0001g0175 a0001c0004t0001g0359 |
2 | HG02257.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1412-371G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456376 | |||||||
chr2:241456412 | T | A | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1412-335T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456412 | |||||||
chr2:241456503 | G | C | 31 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-244G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456503 | |||||||
chr2:241456618 | A | G | 63 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0205 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1412-129A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456618 | |||||||
chr2:241456672 | A | T | 113 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0205 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1412-75A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456672 | |||||||
chr2:241456680 | C | T | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1412-67C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456680 | |||||||
chr2:241456731 | C | T | 2 | a0001c0004t0001g0168 a0001c0004t0001g0176 |
2 | HG02895.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1412-16C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456731 | |||||||
chr2:241456966 | G | A | 3 | a0004c0007t0001g0096 a0004c0007t0001g0097 a0004c0007t0001g0105 |
3 | HG01099.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1587+44G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241456966 | |||||||
chr2:241457011 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0231 others(56): Show |
59 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1587+89G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457011 | |||||||
chr2:241457016 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1587+94G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457016 | |||||||
chr2:241457097 | A | G | 3 | a0001c0001t0001g0098 a0001c0003t0001g0038 a0005c0014t0001g0150 |
3 | HG03098.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1587+175A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457097 | |||||||
chr2:241457156 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1587+234G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457156 | |||||||
chr2:241457251 | T | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(197): Show |
200 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1587+329T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457251 | |||||||
chr2:241457260 | T | G | 1 | a0001c0011t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1587+338T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457260 | |||||||
chr2:241457275 | CCCGT | C | 4 | a0003c0005t0001g0369 a0008c0013t0001g0191 a0009c0012t0001g0001 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+356_1587+359d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457275 | ||||||
chr2:241457278 | G | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0098 others(169): Show |
172 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.1587+356G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457278 | |||||||
chr2:241457279 | T | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0098 others(146): Show |
149 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1587+357T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457279 | |||||||
chr2:241457337 | T | C | 1 | a0001c0006t0001g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1587+415T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457337 | |||||||
chr2:241457351 | G | GGAAAGAT others(74): Show |
3 | a0001c0003t0001g0015 a0001c0003t0001g0016 a0001c0003t0001g0017 |
3 | HG00609.hp1 HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1587+466_1587+467i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | ||||||
chr2:241457351 | G | GGAAAGAT others(74): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+466_1587+467i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | ||||||
chr2:241457351 | G | GGAAAGAT others(74): Show |
2 | a0001c0004t0001g0359 a0010c0020t0001g0155 |
2 | HG00323.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1587+456_1587+536d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | ||||||
chr2:241457356 | GATCTGGG others(398): Show |
G | 9 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(6): Show |
9 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587+467_1587+871d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457356 | ||||||
chr2:241457378 | G | A | 7 | a0001c0001t0001g0103 a0001c0025t0001g0160 a0005c0008t0001g0146 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1587+456G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457378 | |||||||
chr2:241457378 | GCACTAGG others(74): Show |
G | 32 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0003t0001g0007 others(29): Show |
32 | HG00280.hp1 HG01106.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1587+467_1587+547d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457378 | ||||||
chr2:241457378 | GCACTAGG others(236): Show |
G | 5 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(2): Show |
5 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+467_1587+709d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457378 | ||||||
chr2:241457389 | T | C | 53 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0001g0103 others(50): Show |
53 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1587+467T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457389 | |||||||
chr2:241457389 | T | TGCTTTGG others(155): Show |
1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1587+495_1587+496i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | ||||||
chr2:241457389 | T | TGCTTTGG others(155): Show |
1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1587+495_1587+496i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | ||||||
chr2:241457389 | TGCTTTGG others(74): Show |
T | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1587+496_1587+576d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | ||||||
chr2:241457402 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1587+480G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457402 | |||||||
chr2:241457402 | G | GGAGAGGC others(74): Show |
2 | a0001c0001t0002g0372 a0001c0015t0002g0371 |
2 | HG01261.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1587+495_1587+496i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457402 | ||||||
chr2:241457402 | G | GGAGAGGC others(398): Show |
2 | a0001c0001t0002g0373 a0001c0001t0002g0375 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1587+495_1587+496i others(407): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457402 | ||||||
chr2:241457418 | A | G | 22 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0296 others(19): Show |
22 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1587+496A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457418 | |||||||
chr2:241457423 | G | A | 19 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0296 others(16): Show |
19 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1587+501G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457423 | |||||||
chr2:241457423 | G | GCCCAGTG others(155): Show |
1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1587+624_1587+785d others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | G | GCCCAGTG others(155): Show |
2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1587+536_1587+537i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | G | GCCCAGTG others(236): Show |
1 | a0003c0005t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | G | GCCCAGTG others(317): Show |
1 | a0005c0014t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1587+536_1587+537i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | G | GCCCAGTG others(74): Show |
3 | a0001c0010t0001g0363 a0001c0010t0001g0364 a0001c0010t0001g0365 |
3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1587+536_1587+537i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | G | GCCCAGTG others(236): Show |
5 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0003c0005t0001g0049 others(2): Show |
5 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457423 | GCCCAGTG others(155): Show |
G | 11 | a0001c0006t0001g0240 a0001c0006t0001g0241 a0001c0006t0001g0242 others(8): Show |
11 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+624_1587+785d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | ||||||
chr2:241457437 | G | C | 6 | a0001c0001t0001g0103 a0001c0025t0001g0160 a0005c0008t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+515G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457437 | |||||||
chr2:241457437 | G | GATCTGGG others(155): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1587+536_1587+537i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457437 | ||||||
chr2:241457459 | A | ACACTAGG others(155): Show |
1 | a0001c0001t0001g0214 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1587+617_1587+618i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | ||||||
chr2:241457459 | A | ACACTAGG others(74): Show |
1 | a0001c0004t0001g0359 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1587+618_1587+698d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | ||||||
chr2:241457459 | A | ACACTAGG others(155): Show |
1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1587+559_1587+560i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | ||||||
chr2:241457459 | A | ACACTAGG others(74): Show |
2 | a0001c0001t0001g0113 a0017c0026t0001g0118 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1587+547_1587+548i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | ||||||
chr2:241457459 | A | G | 203 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1587+537A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457459 | |||||||
chr2:241457459 | A | GCACTAGG others(236): Show |
1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457459 | |||||||
chr2:241457459 | ACACTAGG others(74): Show |
A | 1 | a0001c0006t0001g0247 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1587+618_1587+698d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | ||||||
chr2:241457465 | G | GGGACTGC others(722): Show |
1 | a0002c0002t0001g0350 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1587+547_1587+548i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457465 | ||||||
chr2:241457470 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0113 a0001c0001t0001g0142 others(80): Show |
83 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1587+548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457470 | |||||||
chr2:241457470 | C | TGCTTTGG others(155): Show |
2 | a0001c0001t0002g0374 a0008c0013t0001g0029 |
2 | HG02559.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1587+547_1587+548i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457470 | |||||||
chr2:241457482 | C | T | 2 | a0001c0001t0001g0378 a0002c0002t0001g0350 |
2 | HG01975.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1587+560C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457482 | |||||||
chr2:241457483 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0142 others(79): Show |
82 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1587+561G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457483 | |||||||
chr2:241457483 | G | GGAGAGGC others(74): Show |
1 | a0001c0001t0001g0296 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1587+576_1587+577i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457483 | ||||||
chr2:241457499 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0142 others(82): Show |
85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1587+577G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457499 | |||||||
chr2:241457504 | A | ACCCAGTG others(722): Show |
3 | a0002c0002t0001g0200 a0002c0002t0001g0358 a0018c0018t0001g0338 |
3 | NA18960.hp1 NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1587+617_1587+618i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | ||||||
chr2:241457504 | A | ACCCAGTG others(2342): Show |
1 | a0002c0002t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1587+617_1587+618i others(2351): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | ||||||
chr2:241457504 | A | ACCCAGTG others(74): Show |
1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587+628_1587+629i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | ||||||
chr2:241457504 | A | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0142 others(82): Show |
85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1587+582A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457504 | |||||||
chr2:241457518 | G | C | 4 | a0001c0001t0001g0072 a0005c0008t0001g0144 a0005c0008t0001g0146 others(1): Show |
4 | HG02074.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+596G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457518 | |||||||
chr2:241457518 | G | GATCTGGG others(317): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0313 |
2 | NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1587+657_1587+658i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457518 | ||||||
chr2:241457518 | G | GATCTGGG others(74): Show |
24 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1587+676_1587+677i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457518 | ||||||
chr2:241457540 | G | A | 43 | a0001c0001t0001g0189 a0001c0001t0001g0205 a0001c0001t0001g0206 others(40): Show |
43 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1587+618G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457540 | |||||||
chr2:241457540 | G | GCACTAAG others(317): Show |
2 | a0002c0002t0001g0347 a0002c0002t0001g0349 |
2 | HG01256.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1587+623_1587+624i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAAG others(803): Show |
1 | a0002c0002t0001g0254 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1587+623_1587+624i others(812): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAAG others(722): Show |
5 | a0002c0002t0001g0256 a0002c0002t0001g0260 a0002c0002t0001g0261 others(2): Show |
5 | HG00639.hp1 HG01175.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+623_1587+624i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAAG others(641): Show |
20 | a0002c0002t0001g0253 a0002c0002t0001g0257 a0002c0002t0001g0258 others(17): Show |
20 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1587+623_1587+624i others(650): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAAG others(642): Show |
1 | a0002c0002t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1587+623_1587+624i others(651): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAAG others(236): Show |
2 | a0002c0002t0001g0336 a0002c0002t0001g0353 |
2 | NA18952.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1587+623_1587+624i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | G | GCACTAGG others(560): Show |
2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1587+657_1587+658i others(569): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457540 | GCACTAGG others(74): Show |
G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0093 a0001c0001t0001g0098 others(2): Show |
5 | HG02486.hp1 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+699_1587+779d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | ||||||
chr2:241457546 | G | A | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+624G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457546 | |||||||
chr2:241457546 | G | GGGACCGC others(74): Show |
1 | a0007c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457546 | ||||||
chr2:241457546 | G | GGGACCGC others(236): Show |
1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1587+698_1587+699i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457546 | ||||||
chr2:241457551 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0378 |
2 | HG01167.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1587+629C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457551 | |||||||
chr2:241457563 | C | CGGAGAGG others(155): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+698_1587+699i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457563 | ||||||
chr2:241457563 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1587+641C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457563 | |||||||
chr2:241457573 | C | T | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+651C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457573 | |||||||
chr2:241457580 | G | A | 33 | a0001c0001t0001g0378 a0001c0003t0001g0007 a0001c0003t0001g0008 others(30): Show |
33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+658G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457580 | |||||||
chr2:241457585 | A | ACCCAGTG others(74): Show |
2 | a0001c0004t0001g0143 a0001c0004t0001g0362 |
2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | ||||||
chr2:241457585 | A | ACCCAGTG others(155): Show |
17 | a0001c0004t0001g0157 a0001c0004t0001g0159 a0001c0004t0001g0161 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.1587+698_1587+699i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | ||||||
chr2:241457585 | A | ACCCAGTG others(74): Show |
3 | a0001c0010t0001g0363 a0001c0010t0001g0364 a0001c0010t0001g0365 |
3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | ||||||
chr2:241457585 | A | G | 40 | a0001c0001t0001g0378 a0001c0003t0001g0007 a0001c0003t0001g0008 others(37): Show |
40 | HG00280.hp1 HG00609.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1587+663A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457585 | |||||||
chr2:241457621 | A | ACACTAGG others(74): Show |
3 | a0005c0008t0001g0144 a0005c0008t0001g0146 a0005c0008t0001g0149 |
3 | HG02647.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1587+705_1587+785d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457621 | ||||||
chr2:241457621 | A | ACACTAGG others(317): Show |
1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1587+785_1587+786i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457621 | ||||||
chr2:241457621 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1587+699A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457621 | |||||||
chr2:241457627 | G | A | 38 | a0001c0004t0001g0361 a0002c0002t0001g0200 a0002c0002t0001g0253 others(35): Show |
38 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1587+705G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457627 | |||||||
chr2:241457644 | C | T | 4 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 others(1): Show |
4 | HG00642.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+722C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457644 | |||||||
chr2:241457644 | CGGAGAGG others(74): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1587+758_1587+838d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457644 | ||||||
chr2:241457654 | C | CTTGGGCG others(155): Show |
21 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0042 others(18): Show |
21 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1587+779_1587+780i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | ||||||
chr2:241457654 | C | CTTGGGCG others(236): Show |
1 | a0003c0005t0001g0044 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1587+785_1587+786i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | ||||||
chr2:241457654 | C | CTTGGGCG others(74): Show |
2 | a0003c0005t0001g0051 a0003c0005t0001g0194 |
2 | HG01934.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1587+785_1587+786i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | ||||||
chr2:241457654 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0142 others(93): Show |
96 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1587+732C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457654 | |||||||
chr2:241457661 | G | A | 2 | a0001c0004t0001g0361 a0001c0004t0001g0370 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1587+739G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457661 | |||||||
chr2:241457666 | A | G | 2 | a0001c0004t0001g0361 a0001c0004t0001g0370 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1587+744A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457666 | |||||||
chr2:241457680 | G | C | 5 | a0001c0001t0001g0158 a0001c0003t0001g0011 a0001c0003t0001g0012 others(2): Show |
5 | HG02622.hp2 NA18954.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+758G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457680 | |||||||
chr2:241457702 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+780G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457702 | |||||||
chr2:241457708 | A | AGGACCGC others(74): Show |
1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1587+802_1587+803i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457708 | ||||||
chr2:241457708 | A | G | 76 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(73): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1587+786A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457708 | |||||||
chr2:241457725 | T | C | 7 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0001g0055 others(4): Show |
7 | HG00642.hp2 HG01243.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+803T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457725 | |||||||
chr2:241457742 | G | A | 4 | a0001c0001t0001g0158 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+820G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457742 | |||||||
chr2:241457747 | A | G | 4 | a0001c0001t0001g0158 a0001c0003t0001g0054 a0001c0003t0001g0055 others(1): Show |
4 | HG00642.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+825A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457747 | |||||||
chr2:241457761 | C | G | 7 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 others(4): Show |
7 | HG00642.hp2 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+839C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457761 | |||||||
chr2:241457789 | G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1587+867G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457789 | |||||||
chr2:241457795 | G | A | 35 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(32): Show |
35 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1587+873G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457795 | |||||||
chr2:241457822 | C | T | 24 | a0001c0001t0001g0268 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1587+900C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457822 | |||||||
chr2:241457877 | G | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(253): Show |
256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1587+955G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457877 | |||||||
chr2:241457904 | A | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1587+982A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457904 | |||||||
chr2:241457960 | G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+1038G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457960 | |||||||
chr2:241458029 | A | G | 13 | a0001c0006t0001g0236 a0001c0006t0001g0240 a0001c0006t0001g0241 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1587+1107A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458029 | |||||||
chr2:241458045 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(88): Show |
91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1587+1123A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458045 | |||||||
chr2:241458326 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1587+1404G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458326 | |||||||
chr2:241458336 | A | G | 2 | a0006c0009t0001g0183 a0006c0009t0001g0184 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1587+1414A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458336 | |||||||
chr2:241458355 | G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1587+1433G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458355 | |||||||
chr2:241458411 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1587+1489G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458411 | |||||||
chr2:241458449 | G | A | 1 | a0002c0002t0001g0341 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1587+1527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458449 | |||||||
chr2:241458601 | G | A | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1587+1679G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458601 | |||||||
chr2:241458659 | T | C | 31 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1587+1737T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458659 | |||||||
chr2:241458681 | C | CA | 57 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0006t0001g0236 others(54): Show |
57 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1587+1770dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241458681 | ||||||
chr2:241458970 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1587+2048G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458970 | |||||||
chr2:241459108 | G | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1587+2186G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459108 | |||||||
chr2:241459262 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1587+2340C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459262 | |||||||
chr2:241459281 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1587+2359G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459281 | |||||||
chr2:241459349 | C | T | 1 | a0005c0008t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1587+2427C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459349 | |||||||
chr2:241459454 | C | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1587+2532C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459454 | |||||||
chr2:241459460 | C | T | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1587+2538C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459460 | |||||||
chr2:241459658 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587+2736T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459658 | |||||||
chr2:241459682 | C | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1587+2760C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459682 | |||||||
chr2:241459708 | C | T | 1 | a0003c0005t0001g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1587+2786C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459708 | |||||||
chr2:241459720 | G | T | 1 | a0001c0006t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1587+2798G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459720 | |||||||
chr2:241459839 | G | A | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1588-2684G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459839 | |||||||
chr2:241459860 | C | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1588-2663C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459860 | |||||||
chr2:241460030 | A | G | 32 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(29): Show |
32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-2493A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460030 | |||||||
chr2:241460071 | A | T | 5 | a0001c0003t0001g0007 a0001c0003t0001g0022 a0001c0003t0001g0023 others(2): Show |
5 | NA18949.hp2 NA18951.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-2452A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460071 | |||||||
chr2:241460078 | C | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(82): Show |
85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1588-2445C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460078 | |||||||
chr2:241460103 | C | G | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1588-2420C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460103 | |||||||
chr2:241460286 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0109 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1588-2237G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460286 | |||||||
chr2:241460312 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1588-2211G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460312 | |||||||
chr2:241460447 | C | CT | 32 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-2064dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241460447 | ||||||
chr2:241460448 | T | G | 87 | a0001c0001t0001g0136 a0001c0001t0001g0205 a0001c0001t0001g0206 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1588-2075T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460448 | |||||||
chr2:241460511 | C | T | 1 | a0001c0001t0009g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1588-2012C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460511 | |||||||
chr2:241460512 | G | A | 119 | a0001c0001t0001g0136 a0001c0001t0001g0205 a0001c0001t0001g0206 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1588-2011G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460512 | |||||||
chr2:241460606 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1588-1917T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460606 | |||||||
chr2:241460685 | A | AG | 91 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(88): Show |
91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1588-1837dupG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241460685 | ||||||
chr2:241460846 | A | G | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1588-1677A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460846 | |||||||
chr2:241460858 | C | T | 3 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0357 |
3 | HG00639.hp1 HG01175.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1588-1665C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460858 | |||||||
chr2:241460875 | C | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1648C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460875 | |||||||
chr2:241460876 | G | C | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1588-1647G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460876 | |||||||
chr2:241460891 | C | G | 1 | a0001c0006t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1588-1632C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460891 | |||||||
chr2:241460968 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1555A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460968 | |||||||
chr2:241461066 | G | C | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1588-1457G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461066 | |||||||
chr2:241461182 | A | G | 62 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1588-1341A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461182 | |||||||
chr2:241461211 | C | T | 1 | a0002c0002t0006g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1588-1312C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461211 | |||||||
chr2:241461238 | G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1588-1285G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461238 | |||||||
chr2:241461265 | A | G | 1 | a0001c0003t0001g0026 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1588-1258A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461265 | |||||||
chr2:241461308 | G | A | 87 | a0001c0001t0001g0136 a0001c0001t0001g0205 a0001c0001t0001g0206 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1588-1215G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461308 | |||||||
chr2:241461330 | C | G | 323 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(320): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1588-1193C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461330 | |||||||
chr2:241461333 | CCT | C | 36 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1588-1185_1588-118 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241461333 | ||||||
chr2:241461421 | C | A | 2 | a0001c0001t0002g0373 a0001c0001t0002g0375 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1588-1102C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461421 | |||||||
chr2:241461422 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461422 | |||||||
chr2:241461432 | TC | T | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588-1087delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241461432 | ||||||
chr2:241461538 | G | A | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1588-985G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461538 | |||||||
chr2:241461587 | T | C | 121 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0205 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1588-936T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461587 | |||||||
chr2:241461630 | G | C | 2 | a0002c0002t0001g0342 a0002c0002t0001g0343 |
2 | NA18988.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1588-893G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461630 | |||||||
chr2:241461722 | A | G | 1 | a0001c0003t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1588-801A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461722 | |||||||
chr2:241461751 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-772C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461751 | |||||||
chr2:241462007 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(88): Show |
91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1588-516C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462007 | |||||||
chr2:241462024 | C | A | 32 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(29): Show |
32 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-499C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462024 | |||||||
chr2:241462024 | C | G | 31 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1588-499C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462024 | |||||||
chr2:241462070 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1588-453G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462070 | |||||||
chr2:241462078 | T | G | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1588-445T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462078 | |||||||
chr2:241462138 | G | A | 2 | a0004c0007t0001g0101 a0004c0007t0001g0102 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1588-385G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462138 | |||||||
chr2:241462144 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1588-379G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462144 | |||||||
chr2:241462238 | A | G | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1588-285A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462238 | |||||||
chr2:241462292 | C | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1588-231C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462292 | |||||||
chr2:241462417 | G | A | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1588-106G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462417 | |||||||
chr2:241462646 | T | A | 31 | a0001c0001t0001g0376 a0001c0004t0001g0143 a0001c0004t0001g0157 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1677+34T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462646 | |||||||
chr2:241462647 | A | T | 88 | a0001c0001t0001g0136 a0001c0001t0001g0205 a0001c0001t0001g0206 others(85): Show |
88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1677+35A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462647 | |||||||
chr2:241462672 | G | C | 29 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1677+60G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462672 | |||||||
chr2:241462745 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1677+133G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462745 | |||||||
chr2:241463048 | C | G | 21 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(18): Show |
21 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1678-287C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463048 | |||||||
chr2:241463178 | A | C | 1 | a0002c0002t0001g0339 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1678-157A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463178 | |||||||
chr2:241463255 | T | G | 1 | a0001c0003t0001g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1678-80T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463255 | |||||||
chr2:241463262 | AG | A | 3 | a0002c0002t0001g0200 a0002c0002t0001g0354 a0002c0002t0001g0358 |
3 | NA18960.hp1 NA18972.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1678-71delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 241463262 | ||||||
chr2:241463488 | C | G | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1811+20C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463488 | |||||||
chr2:241463523 | G | A | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1811+55G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463523 | |||||||
chr2:241463665 | G | T | 1 | a0004c0007t0001g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1811+197G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463665 | |||||||
chr2:241463704 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1812-195A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463704 | |||||||
chr2:241464083 | G | GTCCCCTC others(9): Show |
2 | a0003c0005t0001g0043 a0003c0005t0001g0044 |
2 | NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1893+109_1893+124d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464083 | ||||||
chr2:241464215 | C | T | 1 | a0001c0001t0001g0376 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1893+235C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464215 | |||||||
chr2:241464247 | CTCCTCAA others(42): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1893+279_1893+327d others(51): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464247 | ||||||
chr2:241464355 | G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1893+375G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464355 | |||||||
chr2:241464369 | A | AGAGGGAC others(10): Show |
1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1893+389_1893+390i others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464369 | |||||||
chr2:241464480 | C | T | 1 | a0002c0002t0001g0357 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1893+500C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464480 | |||||||
chr2:241464506 | T | A | 155 | a0001c0001t0001g0158 a0001c0001t0001g0205 a0001c0001t0001g0206 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1893+526T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464506 | |||||||
chr2:241464516 | A | AAGCAGGG others(9): Show |
69 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1893+544_1893+545i others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464516 | ||||||
chr2:241464525 | T | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(175): Show |
178 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1893+545T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464525 | |||||||
chr2:241464588 | G | T | 39 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(36): Show |
39 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1893+608G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464588 | |||||||
chr2:241464591 | CTCTCAGA others(9): Show |
C | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1893+620_1893+635d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464591 | ||||||
chr2:241464720 | G | T | 69 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1893+740G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464720 | |||||||
chr2:241464903 | T | A | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1893+923T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464903 | |||||||
chr2:241465000 | C | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00639.hp2 HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1893+1020C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465000 | |||||||
chr2:241465022 | A | G | 31 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1893+1042A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465022 | |||||||
chr2:241465079 | G | A | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1893+1099G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465079 | |||||||
chr2:241465246 | T | C | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1893+1266T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465246 | |||||||
chr2:241465329 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1893+1349T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465329 | |||||||
chr2:241465353 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1893+1373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465353 | |||||||
chr2:241465606 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1893+1626C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465606 | |||||||
chr2:241465694 | G | C | 1 | a0001c0001t0002g0372 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1893+1714G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465694 | |||||||
chr2:241465737 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1893+1757G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465737 | |||||||
chr2:241465755 | C | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1893+1775C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465755 | |||||||
chr2:241466053 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1893+2073A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466053 | |||||||
chr2:241466106 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1894-2034G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466106 | |||||||
chr2:241466319 | C | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1894-1821C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466319 | |||||||
chr2:241466357 | G | A | 86 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(83): Show |
86 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1894-1783G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466357 | |||||||
chr2:241466455 | C | T | 1 | a0001c0004t0001g0359 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1894-1685C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466455 | |||||||
chr2:241466640 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1894-1500C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466640 | |||||||
chr2:241466657 | G | A | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1894-1483G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466657 | |||||||
chr2:241466689 | A | AC | 66 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0068 others(63): Show |
66 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1894-1440dupC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | ||||||
chr2:241466689 | A | ACC | 17 | a0001c0001t0001g0120 a0001c0003t0001g0007 a0001c0003t0001g0008 others(14): Show |
17 | HG01192.hp1 HG01243.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1894-1441_1894-144 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | ||||||
chr2:241466689 | AC | A | 65 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0209 others(62): Show |
65 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1894-1440delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | ||||||
chr2:241466692 | C | T | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1894-1448C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466692 | |||||||
chr2:241466693 | C | G | 30 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1894-1447C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466693 | |||||||
chr2:241466695 | C | G | 1 | a0003c0005t0001g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1894-1445C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466695 | |||||||
chr2:241466696 | C | G | 1 | a0003c0005t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1894-1444C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466696 | |||||||
chr2:241466698 | C | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(120): Show |
123 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.1894-1442C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466698 | |||||||
chr2:241466698 | C | G | 8 | a0001c0025t0001g0160 a0005c0008t0001g0146 a0005c0008t0001g0147 others(5): Show |
8 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1894-1442C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466698 | |||||||
chr2:241466700 | C | T | 1 | a0001c0004t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1894-1440C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466700 | |||||||
chr2:241466830 | C | T | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1894-1310C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466830 | |||||||
chr2:241466947 | T | TAAA | 23 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(20): Show |
23 | HG00544.hp2 HG00639.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1894-1181_1894-117 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466947 | ||||||
chr2:241467131 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1894-1009T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467131 | |||||||
chr2:241467149 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1894-991G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467149 | |||||||
chr2:241467210 | C | T | 1 | a0008c0013t0001g0029 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1894-930C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467210 | |||||||
chr2:241467239 | G | C | 28 | a0001c0001t0001g0098 a0001c0001t0001g0205 a0001c0001t0001g0206 others(25): Show |
28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1894-901G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467239 | |||||||
chr2:241467455 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1894-685G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467455 | |||||||
chr2:241467495 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1894-645A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467495 | |||||||
chr2:241467566 | C | T | 38 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1894-574C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467566 | |||||||
chr2:241467581 | G | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1894-559G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467581 | |||||||
chr2:241467641 | C | CA | 39 | a0001c0001t0001g0086 a0001c0001t0001g0158 a0001c0001t0001g0205 others(36): Show |
39 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1894-482dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241467641 | ||||||
chr2:241467641 | CA | C | 11 | a0001c0001t0001g0067 a0001c0001t0001g0083 a0001c0001t0001g0136 others(8): Show |
11 | HG02965.hp1 HG03491.hp1 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1894-482delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241467641 | ||||||
chr2:241467764 | G | A | 35 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1894-376G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467764 | |||||||
chr2:241467812 | C | T | 59 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(56): Show |
59 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1894-328C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467812 | |||||||
chr2:241468052 | C | T | 36 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1894-88C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241468052 | |||||||
chr2:241468063 | A | G | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1894-77A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241468063 | |||||||
chr2:241468470 | G | A | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2131+93G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468470 | |||||||
chr2:241468475 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2131+98C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468475 | |||||||
chr2:241468547 | C | G | 1 | a0001c0006t0001g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2131+170C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468547 | |||||||
chr2:241468804 | G | A | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2131+427G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468804 | |||||||
chr2:241468942 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2131+565A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468942 | |||||||
chr2:241469092 | G | GT | 36 | a0001c0001t0001g0142 a0001c0001t0001g0205 a0001c0001t0001g0206 others(33): Show |
36 | HG00423.hp2 HG00639.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.2131+726dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241469092 | ||||||
chr2:241469309 | A | G | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2131+932A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469309 | |||||||
chr2:241469533 | C | T | 7 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0163 others(4): Show |
7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+1156C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469533 | |||||||
chr2:241469566 | T | C | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2131+1189T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469566 | |||||||
chr2:241469912 | C | T | 2 | a0001c0001t0002g0373 a0001c0001t0002g0375 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2131+1535C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469912 | |||||||
chr2:241470068 | C | G | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2131+1691C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470068 | |||||||
chr2:241470145 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2131+1768C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470145 | |||||||
chr2:241470286 | A | G | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2131+1909A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470286 | |||||||
chr2:241470480 | A | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+2103A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470480 | |||||||
chr2:241470518 | A | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+2141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470518 | |||||||
chr2:241470522 | G | C | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2131+2145G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470522 | |||||||
chr2:241470603 | C | T | 29 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+2226C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470603 | |||||||
chr2:241470666 | T | C | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+2289T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470666 | |||||||
chr2:241470708 | AG | A | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2131+2335delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241470708 | ||||||
chr2:241470710 | G | C | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2131+2333G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470710 | |||||||
chr2:241470746 | G | C | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2131+2369G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470746 | |||||||
chr2:241470842 | CAGG | C | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+2466_2131+246 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470842 | |||||||
chr2:241470913 | C | G | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2131+2536C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470913 | |||||||
chr2:241470998 | A | T | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2131+2621A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470998 | |||||||
chr2:241471006 | C | G | 92 | a0001c0003t0001g0027 a0001c0004t0001g0143 a0001c0004t0001g0157 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.2131+2629C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471006 | |||||||
chr2:241471120 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2131+2743T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471120 | |||||||
chr2:241471161 | G | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2131+2784G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471161 | |||||||
chr2:241471203 | T | C | 1 | a0002c0002t0001g0256 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2131+2826T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471203 | |||||||
chr2:241471206 | C | T | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2131+2829C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471206 | |||||||
chr2:241471248 | G | T | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2131+2871G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471248 | |||||||
chr2:241471295 | G | A | 1 | a0007c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2131+2918G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471295 | |||||||
chr2:241471343 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2131+2966C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471343 | |||||||
chr2:241471365 | C | G | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2131+2988C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471365 | |||||||
chr2:241471369 | G | A | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+2992G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471369 | |||||||
chr2:241471459 | T | C | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2131+3082T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471459 | |||||||
chr2:241471483 | C | CT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0063 others(112): Show |
115 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.2131+3130dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | ||||||
chr2:241471483 | C | CTT | 105 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0071 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.2131+3129_2131+313 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | ||||||
chr2:241471483 | C | CTTT | 34 | a0001c0001t0001g0089 a0001c0001t0001g0205 a0001c0001t0001g0206 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2131+3128_2131+313 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | ||||||
chr2:241471483 | CT | C | 12 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0025t0001g0160 others(9): Show |
12 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2131+3130delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | ||||||
chr2:241471506 | T | G | 2 | a0001c0006t0001g0236 a0001c0006t0001g0247 |
2 | NA18984.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2131+3129T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471506 | |||||||
chr2:241471506 | T | TG | 12 | a0001c0001t0001g0142 a0001c0003t0001g0027 a0001c0006t0001g0240 others(9): Show |
12 | HG00408.hp1 HG00621.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2131+3129_2131+313 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471506 | |||||||
chr2:241471533 | A | G | 71 | a0001c0001t0001g0119 a0001c0001t0001g0140 a0001c0001t0001g0205 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.2131+3156A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471533 | |||||||
chr2:241471556 | G | C | 1 | a0003c0005t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2131+3179G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471556 | |||||||
chr2:241471563 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2131+3186G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471563 | |||||||
chr2:241471584 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2131+3207C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471584 | |||||||
chr2:241471618 | C | T | 26 | a0001c0004t0001g0157 a0001c0004t0001g0159 a0001c0004t0001g0161 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.2131+3241C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471618 | |||||||
chr2:241471642 | C | T | 31 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2131+3265C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471642 | |||||||
chr2:241471654 | T | C | 150 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2131+3277T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471654 | |||||||
chr2:241471656 | T | G | 150 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2131+3279T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471656 | |||||||
chr2:241471742 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2131+3365G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471742 | |||||||
chr2:241471775 | A | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+3398A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471775 | |||||||
chr2:241471795 | G | A | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3418G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471795 | |||||||
chr2:241471902 | G | GTTCTGTG others(187): Show |
69 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2131+3550_2131+355 others(198): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471902 | ||||||
chr2:241471902 | G | GTTCTGTG others(187): Show |
50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3537_2131+353 others(198): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471902 | ||||||
chr2:241471992 | A | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2131+3615A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471992 | |||||||
chr2:241472027 | C | T | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3650C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472027 | |||||||
chr2:241472101 | G | A | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3724G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472101 | |||||||
chr2:241472132 | T | C | 6 | a0001c0025t0001g0160 a0005c0008t0001g0146 a0005c0008t0001g0147 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2132-3725T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472132 | |||||||
chr2:241472141 | C | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-3716C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472141 | |||||||
chr2:241472142 | C | G | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-3715C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472142 | |||||||
chr2:241472363 | A | C | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2132-3494A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472363 | |||||||
chr2:241472387 | G | A | 9 | a0001c0025t0001g0160 a0005c0008t0001g0144 a0005c0008t0001g0146 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-3470G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472387 | |||||||
chr2:241472412 | T | C | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-3445T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472412 | |||||||
chr2:241472421 | G | A | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2132-3436G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472421 | |||||||
chr2:241472460 | G | C | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2132-3397G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472460 | |||||||
chr2:241472574 | G | A | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2132-3283G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472574 | |||||||
chr2:241472663 | C | T | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-3194C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472663 | |||||||
chr2:241472694 | T | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0158 a0001c0001t0001g0205 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2132-3163T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472694 | |||||||
chr2:241472785 | A | G | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-3072A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472785 | |||||||
chr2:241472851 | G | A | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2132-3006G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472851 | |||||||
chr2:241472943 | A | C | 86 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(83): Show |
86 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2132-2914A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472943 | |||||||
chr2:241473257 | A | G | 38 | a0001c0001t0001g0158 a0001c0003t0001g0007 a0001c0003t0001g0008 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2132-2600A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473257 | |||||||
chr2:241473480 | G | T | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-2377G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473480 | |||||||
chr2:241473505 | C | T | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2132-2352C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473505 | |||||||
chr2:241473560 | G | C | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2132-2297G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473560 | |||||||
chr2:241473858 | C | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-1999C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473858 | |||||||
chr2:241473888 | A | G | 1 | a0003c0005t0001g0010 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2132-1969A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473888 | |||||||
chr2:241474034 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2132-1823C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474034 | |||||||
chr2:241474238 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2132-1619G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474238 | |||||||
chr2:241474305 | G | A | 1 | a0001c0006t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2132-1552G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474305 | |||||||
chr2:241474317 | C | CA | 12 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0131 others(9): Show |
12 | HG00544.hp1 HG00741.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2132-1507dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CA | C | 9 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0098 others(6): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-1507delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAA | C | 19 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0158 others(16): Show |
19 | HG01106.hp1 HG01934.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2132-1508_2132-150 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAA | C | 91 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(88): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2132-1509_2132-150 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAA | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2132-1510_2132-150 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAA | C | 47 | a0001c0001t0001g0142 a0001c0001t0001g0262 a0001c0001t0001g0263 others(44): Show |
47 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2132-1511_2132-150 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAA | C | 6 | a0001c0004t0001g0359 a0001c0004t0001g0370 a0001c0006t0001g0236 others(3): Show |
6 | HG00609.hp2 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2132-1512_2132-150 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAAA others(1): Show |
C | 29 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(26): Show |
29 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2132-1514_2132-150 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2132-1517_2132-150 others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAAA others(10): Show |
C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2132-1523_2132-150 others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2132-1525_2132-150 others(23): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474317 | CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2132-1526_2132-150 others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | ||||||
chr2:241474493 | A | C | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2132-1364A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474493 | |||||||
chr2:241474528 | C | T | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-1329C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474528 | |||||||
chr2:241474676 | C | T | 4 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0004t0001g0171 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.2132-1181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474676 | |||||||
chr2:241474801 | T | TA | 15 | a0001c0001t0001g0378 a0001c0003t0001g0027 a0001c0006t0001g0236 others(12): Show |
15 | HG00621.hp2 HG01192.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2132-1054dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474801 | T | TAAATA | 34 | a0001c0006t0001g0244 a0002c0002t0001g0200 a0002c0002t0001g0253 others(31): Show |
34 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2132-1054_2132-105 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474801 | T | TAATA | 112 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0071 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2132-1021_2132-101 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474801 | T | TAATAAAT others(1): Show |
69 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(66): Show |
69 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2132-1025_2132-101 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474801 | TAATAAAT others(5): Show |
T | 35 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(32): Show |
35 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2132-1029_2132-101 others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474801 | TAATAAAT others(9): Show |
T | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2132-1033_2132-101 others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | ||||||
chr2:241474807 | A | T | 1 | a0001c0003t0001g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2132-1050A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474807 | |||||||
chr2:241474944 | C | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2132-913C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474944 | |||||||
chr2:241475116 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2132-741A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475116 | |||||||
chr2:241475247 | T | C | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-610T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475247 | |||||||
chr2:241475381 | T | A | 3 | a0005c0008t0001g0144 a0005c0008t0001g0148 a0005c0008t0001g0149 |
3 | HG02647.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2132-476T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475381 | |||||||
chr2:241475411 | G | A | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2132-446G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475411 | |||||||
chr2:241475426 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 |
3 | HG03669.hp1 HG03704.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2132-431C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475426 | |||||||
chr2:241475459 | C | T | 31 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0040 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2132-398C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475459 | |||||||
chr2:241475671 | T | C | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2132-186T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475671 | |||||||
chr2:241476061 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2262+74A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476061 | |||||||
chr2:241476108 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2262+121C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476108 | |||||||
chr2:241476202 | A | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2262+215A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476202 | |||||||
chr2:241476214 | TA | T | 140 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0076 others(137): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2262+248delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241476214 | ||||||
chr2:241476214 | TAA | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0377 a0001c0003t0001g0009 others(4): Show |
7 | HG01167.hp2 HG01256.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2262+247_2262+248d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241476214 | ||||||
chr2:241476215 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2262+228A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476215 | |||||||
chr2:241476310 | C | T | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2262+323C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476310 | |||||||
chr2:241476323 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2262+336G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476323 | |||||||
chr2:241476457 | G | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2262+470G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476457 | |||||||
chr2:241476517 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2262+530G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476517 | |||||||
chr2:241476593 | G | A | 4 | a0001c0004t0001g0143 a0001c0004t0001g0360 a0001c0004t0001g0361 others(1): Show |
4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+606G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476593 | |||||||
chr2:241476594 | C | T | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2262+607C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476594 | |||||||
chr2:241476946 | G | C | 27 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0011 others(24): Show |
27 | HG00609.hp1 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.2262+959G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476946 | |||||||
chr2:241477004 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2262+1017T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477004 | |||||||
chr2:241477123 | C | CT | 17 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0001t0001g0103 others(14): Show |
17 | HG01256.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2262+1157dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | ||||||
chr2:241477123 | C | CTT | 47 | a0001c0003t0001g0027 a0001c0004t0001g0359 a0001c0004t0001g0361 others(44): Show |
47 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2262+1156_2262+115 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | ||||||
chr2:241477123 | C | CTTT | 50 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(47): Show |
50 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2262+1155_2262+115 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | ||||||
chr2:241477123 | CT | C | 10 | a0001c0001t0001g0089 a0001c0001t0001g0158 a0001c0001t0001g0233 others(7): Show |
10 | HG00099.hp1 HG02129.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2262+1157delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | ||||||
chr2:241477354 | T | A | 1 | a0013c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2262+1367T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477354 | |||||||
chr2:241477502 | C | G | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2262+1515C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477502 | |||||||
chr2:241477550 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+1563G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477550 | |||||||
chr2:241477698 | C | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2262+1711C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477698 | |||||||
chr2:241477770 | T | G | 2 | a0001c0003t0001g0020 a0001c0003t0001g0021 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2262+1783T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477770 | |||||||
chr2:241477904 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2262+1917T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477904 | |||||||
chr2:241478193 | G | A | 1 | a0010c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2262+2206G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478193 | |||||||
chr2:241478393 | C | T | 30 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2262+2406C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478393 | |||||||
chr2:241478535 | G | A | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2262+2548G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478535 | |||||||
chr2:241478838 | C | G | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2262+2851C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478838 | |||||||
chr2:241478947 | C | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+2960C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478947 | |||||||
chr2:241478964 | A | T | 1 | a0009c0012t0001g0002 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2262+2977A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478964 | |||||||
chr2:241479082 | G | C | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2262+3095G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479082 | |||||||
chr2:241479203 | T | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2262+3216T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479203 | |||||||
chr2:241479258 | A | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0224 |
2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2262+3271A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479258 | |||||||
chr2:241479360 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0281 a0001c0001t0001g0299 |
3 | NA18949.hp1 NA18990.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2262+3373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479360 | |||||||
chr2:241479361 | G | A | 2 | a0002c0002t0001g0256 a0011c0017t0001g0255 |
2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2262+3374G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479361 | |||||||
chr2:241479393 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2262+3406G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479393 | |||||||
chr2:241479393 | G | T | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2262+3406G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479393 | |||||||
chr2:241479453 | G | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+3466G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479453 | |||||||
chr2:241479545 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2262+3558C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479545 | |||||||
chr2:241479734 | GT | G | 30 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2263-3730delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479734 | |||||||
chr2:241480247 | CTCA | C | 29 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2263-3215_2263-321 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241480247 | ||||||
chr2:241480249 | C | T | 2 | a0001c0003t0001g0038 a0005c0014t0001g0150 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2263-3216C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480249 | |||||||
chr2:241480452 | G | A | 31 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2263-3013G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480452 | |||||||
chr2:241480532 | GT | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(280): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2263-2922delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241480532 | ||||||
chr2:241480599 | C | T | 1 | a0002c0002t0001g0253 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2263-2866C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480599 | |||||||
chr2:241480770 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2263-2695T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480770 | |||||||
chr2:241480979 | G | A | 29 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2263-2486G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480979 | |||||||
chr2:241481007 | C | G | 33 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2263-2458C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481007 | |||||||
chr2:241481034 | C | T | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2263-2431C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481034 | |||||||
chr2:241481056 | C | CA | 13 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0127 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2263-2384dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | ||||||
chr2:241481056 | CA | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(162): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2263-2384delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | ||||||
chr2:241481056 | CAA | C | 64 | a0001c0001t0001g0158 a0001c0001t0001g0275 a0001c0003t0001g0007 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2263-2385_2263-238 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | ||||||
chr2:241481056 | CAAAAAAA | C | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2263-2390_2263-238 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | ||||||
chr2:241481056 | CAAAAAAA others(3): Show |
C | 36 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2263-2393_2263-238 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | ||||||
chr2:241481556 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2263-1909G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481556 | |||||||
chr2:241481683 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2263-1782C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481683 | |||||||
chr2:241481899 | G | A | 86 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(83): Show |
86 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2263-1566G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481899 | |||||||
chr2:241482451 | G | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(280): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2263-1014G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482451 | |||||||
chr2:241482457 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2263-1008C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482457 | |||||||
chr2:241482550 | C | T | 9 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(6): Show |
9 | HG01496.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2263-915C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482550 | |||||||
chr2:241482676 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2263-789T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482676 | |||||||
chr2:241482734 | C | T | 3 | a0002c0002t0001g0200 a0002c0002t0001g0354 a0002c0002t0001g0358 |
3 | NA18960.hp1 NA18972.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2263-731C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482734 | |||||||
chr2:241482969 | TTGGTGCT others(55): Show |
T | 26 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2263-476_2263-415d others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241482969 | ||||||
chr2:241482989 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2263-476C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482989 | |||||||
chr2:241482989 | CGGGAGAA others(55): Show |
C | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2263-475_2263-414d others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482989 | |||||||
chr2:241482990 | G | A | 254 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2263-475G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482990 | |||||||
chr2:241483031 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2263-434C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483031 | |||||||
chr2:241483252 | G | A | 1 | a0001c0003t0001g0009 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2263-213G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483252 | |||||||
chr2:241483358 | C | T | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2263-107C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483358 | |||||||
chr2:241483373 | G | A | 2 | a0009c0012t0001g0001 a0009c0012t0001g0002 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2263-92G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483373 | |||||||
chr2:241483381 | G | A | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2263-84G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483381 | |||||||
chr2:241483442 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2263-23G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483442 | |||||||
chr2:241483649 | A | G | 1 | a0001c0003t0001g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2331+116A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241483649 | |||||||
chr2:241483672 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2331+139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241483672 | |||||||
chr2:241484133 | A | G | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2332-109A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241484133 | |||||||
chr2:241484498 | T | A | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2421+167T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484498 | |||||||
chr2:241484695 | T | C | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2421+364T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484695 | |||||||
chr2:241484729 | G | A | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2421+398G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484729 | |||||||
chr2:241484762 | TC | T | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2421+433delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241484762 | ||||||
chr2:241484930 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2421+599G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484930 | |||||||
chr2:241484968 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2421+637C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484968 | |||||||
chr2:241485272 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2421+941A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485272 | |||||||
chr2:241485551 | G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2421+1220G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485551 | |||||||
chr2:241485638 | C | A | 6 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0002g0374 others(3): Show |
6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2421+1307C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485638 | |||||||
chr2:241485819 | G | A | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2421+1488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485819 | |||||||
chr2:241485822 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0086 |
3 | NA18961.hp2 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2421+1491C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485822 | |||||||
chr2:241485969 | G | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2421+1638G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485969 | |||||||
chr2:241485977 | C | T | 7 | a0003c0005t0001g0010 a0003c0005t0001g0039 a0003c0005t0001g0052 others(4): Show |
7 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2421+1646C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485977 | |||||||
chr2:241486170 | T | G | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2421+1839T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486170 | |||||||
chr2:241486287 | C | CT | 118 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0206 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2421+1978dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | ||||||
chr2:241486287 | C | CTT | 26 | a0001c0001t0001g0158 a0001c0003t0001g0027 a0001c0003t0001g0060 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2421+1977_2421+197 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | ||||||
chr2:241486287 | CT | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0134 a0001c0001t0001g0188 others(9): Show |
12 | HG00323.hp1 HG00558.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2421+1978delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | ||||||
chr2:241486410 | C | T | 11 | a0004c0007t0001g0096 a0004c0007t0001g0097 a0004c0007t0001g0100 others(8): Show |
11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2421+2079C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486410 | |||||||
chr2:241486461 | C | CA | 12 | a0001c0001t0001g0284 a0001c0001t0001g0310 a0001c0001t0001g0376 others(9): Show |
12 | HG00735.hp2 HG01123.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2421+2156dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | ||||||
chr2:241486461 | CA | C | 180 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2421+2156delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | ||||||
chr2:241486461 | CAA | C | 116 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(113): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2421+2155_2421+215 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | ||||||
chr2:241486524 | C | CATT | 322 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(319): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2421+2193_2421+219 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486524 | |||||||
chr2:241486602 | G | C | 1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2421+2271G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486602 | |||||||
chr2:241486885 | G | C | 11 | a0004c0007t0001g0096 a0004c0007t0001g0097 a0004c0007t0001g0100 others(8): Show |
11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2421+2554G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486885 | |||||||
chr2:241486933 | AAGCAGCC others(6): Show |
A | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2421+2615_2421+262 others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486933 | ||||||
chr2:241486956 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2421+2625A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486956 | |||||||
chr2:241486984 | G | A | 39 | a0001c0001t0001g0098 a0001c0001t0001g0378 a0001c0001t0002g0372 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2421+2653G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486984 | |||||||
chr2:241487005 | CCT | C | 30 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2421+2675_2421+267 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487005 | |||||||
chr2:241487012 | C | T | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2421+2681C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487012 | |||||||
chr2:241487048 | A | G | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2421+2717A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487048 | |||||||
chr2:241487108 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2421+2777G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487108 | |||||||
chr2:241487277 | A | G | 36 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2422-2685A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487277 | |||||||
chr2:241487529 | G | A | 3 | a0001c0010t0001g0363 a0001c0010t0001g0364 a0001c0010t0001g0365 |
3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2422-2433G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487529 | |||||||
chr2:241487588 | A | ACCTGGGA others(43): Show |
91 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(88): Show |
91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.2422-2367_2422-231 others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487588 | ||||||
chr2:241487666 | C | CA | 333 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(330): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2422-2282dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487666 | ||||||
chr2:241487746 | C | CTTTTT | 62 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(59): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2422-2199_2422-219 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487746 | C | CTTTTTT | 51 | a0001c0001t0001g0084 a0001c0001t0001g0210 a0001c0001t0001g0214 others(48): Show |
51 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2422-2200_2422-219 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487746 | C | CTTTTTTT | 137 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2422-2201_2422-219 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487746 | C | CTTTTTTT others(1): Show |
57 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0081 others(54): Show |
57 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2422-2202_2422-219 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487746 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0158 a0001c0001t0001g0330 a0001c0003t0001g0008 others(10): Show |
13 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2422-2203_2422-219 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487746 | C | CTTTTTTT others(3): Show |
1 | a0001c0003t0001g0031 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2422-2204_2422-219 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | ||||||
chr2:241487840 | C | G | 1 | a0001c0001t0002g0372 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2422-2122C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487840 | |||||||
chr2:241487938 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2422-2024C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487938 | |||||||
chr2:241487984 | G | A | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422-1978G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487984 | |||||||
chr2:241488023 | C | A | 1 | a0001c0001t0001g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2422-1939C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488023 | |||||||
chr2:241488046 | C | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2422-1916C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488046 | |||||||
chr2:241488166 | G | GA | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2422-1791dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241488166 | ||||||
chr2:241488174 | G | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2422-1788G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488174 | |||||||
chr2:241488416 | G | GT | 66 | a0001c0001t0001g0075 a0001c0001t0001g0127 a0001c0001t0001g0281 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.2422-1527dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241488416 | ||||||
chr2:241488550 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2422-1412G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488550 | |||||||
chr2:241488590 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2422-1372C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488590 | |||||||
chr2:241488604 | G | T | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-1358G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488604 | |||||||
chr2:241488611 | A | G | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-1351A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488611 | |||||||
chr2:241488638 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2422-1324G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488638 | |||||||
chr2:241488642 | C | T | 5 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0213 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2422-1320C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488642 | |||||||
chr2:241488646 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2422-1316C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488646 | |||||||
chr2:241488679 | T | C | 34 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2422-1283T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488679 | |||||||
chr2:241488691 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2422-1271T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488691 | |||||||
chr2:241488701 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0231 others(80): Show |
83 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.2422-1261A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488701 | |||||||
chr2:241488968 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0093 |
2 | HG03491.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2422-994C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488968 | |||||||
chr2:241489098 | A | G | 28 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(25): Show |
28 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2422-864A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489098 | |||||||
chr2:241489171 | G | C | 50 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2422-791G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489171 | |||||||
chr2:241489305 | T | C | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422-657T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489305 | |||||||
chr2:241489387 | A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2422-575A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489387 | |||||||
chr2:241489394 | G | T | 119 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2422-568G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489394 | |||||||
chr2:241489426 | G | A | 1 | a0012c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2422-536G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489426 | |||||||
chr2:241489495 | G | A | 110 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2422-467G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489495 | |||||||
chr2:241489498 | G | A | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.2422-464G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489498 | |||||||
chr2:241489657 | C | T | 30 | a0001c0004t0001g0143 a0001c0004t0001g0157 a0001c0004t0001g0159 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2422-305C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489657 | |||||||
chr2:241489744 | G | C | 1 | a0006c0009t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2422-218G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489744 | |||||||
chr2:241489820 | T | G | 3 | a0001c0004t0001g0175 a0001c0004t0001g0359 a0001c0004t0001g0370 |
3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-142T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489820 | |||||||
chr2:241490077 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2504+33C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490077 | |||||||
chr2:241490112 | G | A | 1 | a0019c0024t0001g0087 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2504+68G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490112 | |||||||
chr2:241490217 | G | A | 14 | a0001c0003t0001g0027 a0001c0006t0001g0236 a0001c0006t0001g0240 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2504+173G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490217 | |||||||
chr2:241490392 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2504+348G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490392 | |||||||
chr2:241490443 | CCCAGCCC others(2): Show |
C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0201 others(89): Show |
92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2504+403_2504+411d others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 241490443 | ||||||
chr2:241490550 | A | G | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2504+506A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490550 | |||||||
chr2:241490658 | C | T | 1 | a0014c0029t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2505-403C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490658 | |||||||
chr2:241490669 | C | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2505-392C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490669 | |||||||
chr2:241490670 | C | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(122): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2505-391C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490670 | |||||||
chr2:241490755 | C | T | 77 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(74): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2505-306C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490755 | |||||||
chr2:241490830 | C | G | 36 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2505-231C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490830 | |||||||
chr2:241490911 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2505-150G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490911 | |||||||
chr2:241491205 | G | C | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2623+26G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491205 | |||||||
chr2:241491306 | T | G | 2 | a0001c0003t0001g0016 a0001c0003t0001g0017 |
2 | HG00609.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2623+127T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491306 | |||||||
chr2:241491324 | C | A | 9 | a0003c0005t0001g0190 a0003c0005t0001g0192 a0003c0005t0001g0193 others(6): Show |
9 | HG01496.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+145C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491324 | |||||||
chr2:241491746 | TGAG | T | 36 | a0002c0002t0001g0200 a0002c0002t0001g0253 a0002c0002t0001g0254 others(33): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2787+72_2787+74del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr2 | 241491746 | ||||||
chr2:241492030 | C | T | 55 | a0001c0001t0001g0234 a0001c0001t0001g0237 a0001c0001t0001g0238 others(52): Show |
55 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2787+351C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492030 | |||||||
chr2:241492093 | G | T | 1 | a0001c0003t0001g0027 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2787+414G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492093 | |||||||
chr2:241492170 | C | G | 28 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(25): Show |
28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2787+491C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492170 | |||||||
chr2:241492409 | G | A | 1 | a0001c0003t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2788-520G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492409 | |||||||
chr2:241492534 | G | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2788-395G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492534 | |||||||
chr2:241492575 | C | A | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(35): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2788-354C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492575 | |||||||
chr2:241492696 | T | C | 1 | a0008c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2788-233T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492696 | |||||||
chr2:241492727 | T | C | 27 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2788-202T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492727 | |||||||
chr2:241493115 | G | GTATT | 4 | a0003c0005t0001g0040 a0003c0005t0001g0041 a0003c0005t0001g0049 others(1): Show |
4 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2895+81_2895+84dup others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr2 | 241493115 | ||||||
chr2:241493192 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2896-101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493192 | |||||||
chr2:241493214 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2896-79G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493214 | |||||||
chr2:241493289 | G | C | 110 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
splice_region_variant&intron_variant | LOW | c.2896-4G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493289 | |||||||
chr2:241493597 | G | GT | 90 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0142 others(87): Show |
90 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.3047+167dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | ||||||
chr2:241493597 | G | GTT | 8 | a0001c0001t0001g0263 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG01255.hp1 HG02976.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.3047+166_3047+167d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | ||||||
chr2:241493597 | GT | G | 107 | a0001c0001t0001g0137 a0001c0001t0001g0205 a0001c0001t0001g0206 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3047+167delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | ||||||
chr2:241493655 | T | A | 1 | a0001c0003t0001g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3047+211T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | chr2 | 241493655 | |||||||
chr2:241493933 | A | G | 324 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.3048-75A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | chr2 | 241493933 |