Item | Value |
---|---|
geneid | 90342 |
ensemblid | ENSG00000249715.13 |
hgncid | 19044 |
symbol | FER1L5 |
name | fer-1 like family member 5 |
refseq_nuc | NM_001293083.2 |
refseq_prot | NP_001280012.1 |
ensembl_nuc | ENST00000624922.6 |
ensembl_prot | ENSP00000485238.1 |
mane_status | MANE Select |
chr | chr2 |
start | 96642764 |
end | 96704883 |
strand | + |
ver | v1.2 |
region | chr2:96642764-96704883 |
region5000 | chr2:96637764-96709883 |
regionname0 | FER1L5_chr2_96642764_96704883 |
regionname5000 | FER1L5_chr2_96637764_96709883 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2057 | 125 | 60 | 22 | 32 | 5 | 6 | 21 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0002 | 1/1 | 2057 | 68 | 7 | 14 | 29 | 6 | 10 | 19 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0003 | 0/0 | 2057 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0004 | 0/0 | 2057 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0005 | 0/0 | 2057 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0006 | 0/0 | 2057 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0007 | 0/0 | 2057 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0008 | 0/0 | 2057 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0009 | 0/0 | 398 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(393): Show |
chr2 | 96637764 | 96709883 |
a0010 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0011 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0012 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0013 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0014 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0015 | 0/0 | 2057 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
a0016 | 0/0 | 246 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(241): Show |
chr2 | 96637764 | 96709883 |
a0017 | 0/0 | 2057 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | MLRLV others(2052): Show |
chr2 | 96637764 | 96709883 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 6171 | 61 | 16 | 17 | 20 | 5 | 3 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0001c0003 | 0/0 | 6171 | 36 | 35 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0001c0004 | 0/0 | 6171 | 25 | 9 | 4 | 10 | 0 | 2 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0001c0020 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0001c0023 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0001c0024 | 0/0 | 6171 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0002c0001 | 1/1 | 6171 | 61 | 6 | 14 | 24 | 6 | 9 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0002c0006 | 0/0 | 6171 | 6 | 0 | 0 | 5 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0002c0017 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0003c0005 | 0/0 | 6171 | 10 | 9 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0004c0009 | 0/0 | 6171 | 2 | 2 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0004c0012 | 0/0 | 6171 | 2 | 2 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0004c0013 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0005c0007 | 0/0 | 6171 | 3 | 3 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0006c0011 | 0/0 | 6171 | 2 | 0 | 1 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0007c0008 | 0/0 | 6171 | 2 | 0 | 2 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0008c0010 | 0/0 | 6171 | 2 | 0 | 0 | 2 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0009c0025 | 0/0 | 6160 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6155): Show |
chr2 | 96637764 | 96709883 | ||
a0010c0016 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0011c0018 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0012c0022 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0013c0019 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0014c0021 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0015c0015 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0016c0026 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 | ||
a0017c0014 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | ATGCT others(6166): Show |
chr2 | 96637764 | 96709883 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 6438 | 60 | 15 | 17 | 20 | 5 | 3 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0002t0002 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0003t0001 | 0/0 | 6438 | 35 | 34 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0003t0003 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0004t0001 | 0/0 | 6438 | 25 | 9 | 4 | 10 | 0 | 2 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0020t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0023t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0001c0024t0001 | 0/0 | 6438 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0002c0001t0001 | 1/1 | 6438 | 61 | 6 | 14 | 24 | 6 | 9 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0002c0006t0001 | 0/0 | 6438 | 6 | 0 | 0 | 5 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0002c0017t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0003c0005t0001 | 0/0 | 6438 | 10 | 9 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0004c0009t0001 | 0/0 | 6438 | 2 | 2 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0004c0012t0001 | 0/0 | 6438 | 2 | 2 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0004c0013t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0005c0007t0001 | 0/0 | 6438 | 3 | 3 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0006c0011t0001 | 0/0 | 6438 | 2 | 0 | 1 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0007c0008t0001 | 0/0 | 6438 | 2 | 0 | 2 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0008c0010t0001 | 0/0 | 6438 | 2 | 0 | 0 | 2 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0009c0025t0001 | 0/0 | 6427 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6422): Show |
chr2 | 96637764 | 96709883 |
a0010c0016t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0011c0018t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0012c0022t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0013c0019t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0014c0021t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0015c0015t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0016c0026t0001 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
a0017c0014t0001 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | CTTGG others(6433): Show |
chr2 | 96637764 | 96709883 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0020t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0023t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0001c0024t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0002c0017t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0003c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0004c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0004c0009t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0004c0012t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0004c0012t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0004c0013t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0005c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0005c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0005c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0006c0011t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0006c0011t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0007c0008t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0007c0008t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0008c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0008c0010t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0009c0025t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0010c0016t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0011c0018t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0012c0022t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0013c0019t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0014c0021t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0015c0015t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0016c0026t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
a0017c0014t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0009 | c0025 | t0001 | g0153 | EUR | GBR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0058 | EUR | GBR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0165 | EUR | GBR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0097 | EUR | GBR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00323 | hp1 | a0002 | c0001 | t0001 | g0041 | EUR | FIN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0056 | EUR | FIN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00597 | hp1 | a0010 | c0016 | t0001 | g0113 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00597 | hp2 | a0001 | c0004 | t0001 | g0108 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0210 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0067 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0194 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0063 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0132 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01243 | hp2 | a0006 | c0011 | t0001 | g0216 | AMR | PUR | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0168 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0163 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01358 | hp2 | a0003 | c0005 | t0001 | g0212 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0193 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0053 | EUR | IBS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0147 | EUR | IBS | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0159 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01975 | hp2 | a0007 | c0008 | t0001 | g0133 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0142 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02004 | hp2 | a0007 | c0008 | t0001 | g0129 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0060 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02055 | hp1 | a0011 | c0018 | t0001 | g0190 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02055 | hp2 | a0002 | c0001 | t0001 | g0149 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02132 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | KHV | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02145 | hp1 | a0005 | c0007 | t0001 | g0139 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02145 | hp2 | a0004 | c0009 | t0001 | g0035 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | CDX | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | CDX | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CDX | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02165 | hp2 | a0006 | c0011 | t0001 | g0136 | EAS | CDX | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0201 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0090 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02258 | hp2 | a0003 | c0005 | t0001 | g0070 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02280 | hp2 | a0002 | c0001 | t0001 | g0145 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0143 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0195 | AMR | PEL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0127 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02602 | hp2 | a0002 | c0006 | t0001 | g0061 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0045 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0037 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02717 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02717 | hp2 | a0004 | c0009 | t0001 | g0125 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02886 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0054 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02895 | hp2 | a0003 | c0005 | t0001 | g0076 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02896 | hp1 | a0004 | c0012 | t0001 | g0005 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02897 | hp1 | a0004 | c0012 | t0001 | g0004 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02897 | hp2 | a0003 | c0005 | t0001 | g0077 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02922 | hp1 | a0003 | c0005 | t0001 | g0183 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0074 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0213 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0175 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03017 | hp2 | a0001 | c0004 | t0001 | g0018 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03041 | hp1 | a0003 | c0005 | t0001 | g0072 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03130 | hp2 | a0002 | c0001 | t0001 | g0224 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03139 | hp1 | a0003 | c0005 | t0001 | g0071 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03195 | hp2 | a0002 | c0001 | t0001 | g0223 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03209 | hp1 | a0012 | c0022 | t0001 | g0182 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03209 | hp2 | a0005 | c0007 | t0001 | g0217 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03225 | hp1 | a0003 | c0005 | t0001 | g0069 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03486 | hp2 | a0005 | c0007 | t0001 | g0138 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0200 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | GWD | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03579 | hp1 | a0013 | c0019 | t0001 | g0075 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | MSL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0177 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03669 | hp1 | a0001 | c0024 | t0001 | g0021 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0166 | SAS | PJL | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0150 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0154 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0160 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG04184 | hp2 | a0001 | c0004 | t0001 | g0015 | SAS | BEB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18612 | hp1 | a0008 | c0010 | t0001 | g0148 | EAS | CHB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18612 | hp2 | a0002 | c0006 | t0001 | g0048 | EAS | CHB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | CHB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | CHB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0180 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18906 | hp2 | a0004 | c0013 | t0001 | g0019 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18942 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18945 | hp2 | a0002 | c0006 | t0001 | g0049 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18950 | hp1 | a0001 | c0004 | t0001 | g0033 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18962 | hp1 | a0008 | c0010 | t0001 | g0140 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18962 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18963 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18963 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0161 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18970 | hp1 | a0002 | c0006 | t0001 | g0043 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18970 | hp2 | a0014 | c0021 | t0001 | g0146 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18973 | hp2 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18979 | hp2 | a0002 | c0006 | t0001 | g0051 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18981 | hp2 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18982 | hp2 | a0002 | c0006 | t0001 | g0032 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18986 | hp1 | a0001 | c0020 | t0001 | g0025 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18986 | hp2 | a0015 | c0015 | t0001 | g0135 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19011 | hp1 | a0016 | c0026 | t0001 | g0219 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19030 | hp1 | a0017 | c0014 | t0001 | g0225 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0181 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19043 | hp2 | a0002 | c0017 | t0001 | g0046 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19070 | hp2 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19077 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19080 | hp1 | a0001 | c0004 | t0001 | g0022 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19080 | hp2 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19085 | hp2 | a0001 | c0023 | t0001 | g0065 | EAS | JPT | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19240 | hp1 | a0003 | c0005 | t0001 | g0068 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | YRI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | ASW | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | ASW | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0064 | EUR | TSI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0092 | EUR | TSI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20805 | hp1 | a0002 | c0001 | t0001 | g0055 | EUR | TSI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0112 | EUR | TSI | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01123 | hp1 | a0001 | c0004 | t0001 | g0047 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | ACB | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | USA | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | USA | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0083 | AFR | USA | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | USA | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0031 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | LWK | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0057 | REF | REF | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0172 | REF | REF | FER1L5_chr2_96637764_96709883 | FER1L5 | chr2 | 96637764 | 96709883 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96654488 | A | T | 1 | a0016 | 1 | NA19011.hp1 | stop_gained | HIGH | c.739A>T | p.Arg247* | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/53 | 812/6438 | 739/6174 | 247/2057 | chr2 | 96654488 | |||
chr2:96661717 | TCAAGTCA others(4): Show |
T | 1 | a0009 | 1 | HG00099.hp1 | frameshift_variant | HIGH | c.945_955delCAAGTCAG others(3): Show |
p.Lys316fs | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1018/6438 | 945/6174 | 315/2057 | chr2 | 96661717 | |||
chr2:96661731 | G | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.958G>T | p.Val320Phe | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1031/6438 | 958/6174 | 320/2057 | chr2 | 96661731 | |||
chr2:96661732 | T | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.959T>A | p.Val320Asp | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1032/6438 | 959/6174 | 320/2057 | chr2 | 96661732 | |||
chr2:96661735 | C | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.962C>A | p.Pro321Gln | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1035/6438 | 962/6174 | 321/2057 | chr2 | 96661735 | |||
chr2:96661741 | A | C | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.968A>C | p.Asn323Thr | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1041/6438 | 968/6174 | 323/2057 | chr2 | 96661741 | |||
chr2:96661743 | A | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.970A>T | p.Met324Leu | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1043/6438 | 970/6174 | 324/2057 | chr2 | 96661743 | |||
chr2:96661745 | G | C | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.972G>C | p.Met324Ile | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1045/6438 | 972/6174 | 324/2057 | chr2 | 96661745 | |||
chr2:96661746 | G | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.973G>T | p.Ala325Ser | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1046/6438 | 973/6174 | 325/2057 | chr2 | 96661746 | |||
chr2:96661751 | C | G | 1 | a0009 | 1 | HG00099.hp1 | stop_gained | HIGH | c.978C>G | p.Tyr326* | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1051/6438 | 978/6174 | 326/2057 | chr2 | 96661751 | |||
chr2:96661752 | T | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.979T>A | p.Leu327Ile | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1052/6438 | 979/6174 | 327/2057 | chr2 | 96661752 | |||
chr2:96661753 | T | G | 1 | a0009 | 1 | HG00099.hp1 | stop_gained | HIGH | c.980T>G | p.Leu327* | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1053/6438 | 980/6174 | 327/2057 | chr2 | 96661753 | |||
chr2:96661755 | C | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.982C>A | p.Gln328Lys | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1055/6438 | 982/6174 | 328/2057 | chr2 | 96661755 | |||
chr2:96661756 | A | G | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.983A>G | p.Gln328Arg | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1056/6438 | 983/6174 | 328/2057 | chr2 | 96661756 | |||
chr2:96661759 | T | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.986T>A | p.Leu329His | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1059/6438 | 986/6174 | 329/2057 | chr2 | 96661759 | |||
chr2:96661766 | C | G | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.993C>G | p.Ile331Met | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1066/6438 | 993/6174 | 331/2057 | chr2 | 96661766 | |||
chr2:96661767 | T | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.994T>A | p.Tyr332Asn | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1067/6438 | 994/6174 | 332/2057 | chr2 | 96661767 | |||
chr2:96661769 | C | G | 1 | a0009 | 1 | HG00099.hp1 | stop_gained | HIGH | c.996C>G | p.Tyr332* | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1069/6438 | 996/6174 | 332/2057 | chr2 | 96661769 | |||
chr2:96661773 | G | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1000G>T | p.Ala334Ser | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1073/6438 | 1000/6174 | 334/2057 | chr2 | 96661773 | |||
chr2:96661776 | G | T | 1 | a0009 | 1 | HG00099.hp1 | stop_gained | HIGH | c.1003G>T | p.Glu335* | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1076/6438 | 1003/6174 | 335/2057 | chr2 | 96661776 | |||
chr2:96661779 | G | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1006G>A | p.Asp336Asn | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1079/6438 | 1006/6174 | 336/2057 | chr2 | 96661779 | |||
chr2:96661782 | C | G | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1009C>G | p.Leu337Val | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1082/6438 | 1009/6174 | 337/2057 | chr2 | 96661782 | |||
chr2:96661783 | T | G | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1010T>G | p.Leu337Arg | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1083/6438 | 1010/6174 | 337/2057 | chr2 | 96661783 | |||
chr2:96661785 | C | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1012C>T | p.His338Tyr | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1085/6438 | 1012/6174 | 338/2057 | chr2 | 96661785 | |||
chr2:96661786 | A | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1013A>T | p.His338Leu | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1086/6438 | 1013/6174 | 338/2057 | chr2 | 96661786 | |||
chr2:96661789 | T | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant&splice_region_variant | MODERATE | c.1016T>A | p.Leu339His | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1089/6438 | 1016/6174 | 339/2057 | chr2 | 96661789 | |||
chr2:96662257 | T | C | 1 | a0007 | 2 | HG01975.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.1061T>C | p.Ile354Thr | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/53 | 1134/6438 | 1061/6174 | 354/2057 | chr2 | 96662257 | |||
chr2:96685998 | T | C | 1 | a0004 | 5 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.1954T>C | p.Trp652Arg | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 22/53 | 2027/6438 | 1954/6174 | 652/2057 | chr2 | 96685998 | |||
chr2:96686103 | A | G | 10 | a0001 a0003 a0004 others(7): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
missense_variant | MODERATE | c.2059A>G | p.Thr687Ala | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 22/53 | 2132/6438 | 2059/6174 | 687/2057 | chr2 | 96686103 | |||
chr2:96686240 | G | A | 1 | a0017 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2119G>A | p.Glu707Lys | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/53 | 2192/6438 | 2119/6174 | 707/2057 | chr2 | 96686240 | |||
chr2:96689289 | T | C | 3 | a0006 a0008 a0015 |
5 | HG01243.hp2 HG02165.hp2 NA18612.hp1 others(2): Show |
missense_variant | MODERATE | c.2438T>C | p.Met813Thr | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 25/53 | 2511/6438 | 2438/6174 | 813/2057 | chr2 | 96689289 | |||
chr2:96691312 | G | A | 1 | a0015 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.2866G>A | p.Glu956Lys | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 28/53 | 2939/6438 | 2866/6174 | 956/2057 | chr2 | 96691312 | |||
chr2:96691922 | C | A | 1 | a0011 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.3173C>A | p.Thr1058Asn | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 30/53 | 3246/6438 | 3173/6174 | 1058/2057 | chr2 | 96691922 | |||
chr2:96693685 | T | G | 2 | a0003 a0013 |
11 | HG01358.hp2 HG02258.hp2 HG02895.hp2 others(8): Show |
missense_variant&splice_region_variant | MODERATE | c.3472T>G | p.Trp1158Gly | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 32/53 | 3545/6438 | 3472/6174 | 1158/2057 | chr2 | 96693685 | |||
chr2:96695641 | T | C | 1 | a0010 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.3874T>C | p.Ser1292Pro | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 35/53 | 3947/6438 | 3874/6174 | 1292/2057 | chr2 | 96695641 | |||
chr2:96697678 | G | A | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.4153G>A | p.Val1385Met | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 39/53 | 4226/6438 | 4153/6174 | 1385/2057 | chr2 | 96697678 | |||
chr2:96698104 | A | G | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.4304A>G | p.Lys1435Arg | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 40/53 | 4377/6438 | 4304/6174 | 1435/2057 | chr2 | 96698104 | |||
chr2:96702718 | C | T | 1 | a0012 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.5374C>T | p.Arg1792Cys | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 48/53 | 5447/6438 | 5374/6174 | 1792/2057 | chr2 | 96702718 | |||
chr2:96703624 | T | A | 1 | a0005 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.5793T>A | p.His1931Gln | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/53 | 5866/6438 | 5793/6174 | 1931/2057 | chr2 | 96703624 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96661694 | C | T | 1 | a0004c0012 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.921C>T | p.Thr307Thr | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 994/6438 | 921/6174 | 307/2057 | chr2 | 96661694 | |||
chr2:96661736 | G | T | 1 | a0009c0025 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.963G>T | p.Pro321Pro | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1036/6438 | 963/6174 | 321/2057 | chr2 | 96661736 | |||
chr2:96661760 | C | A | 1 | a0009c0025 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.987C>A | p.Leu329Leu | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1060/6438 | 987/6174 | 329/2057 | chr2 | 96661760 | |||
chr2:96661763 | C | T | 1 | a0009c0025 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.990C>T | p.Phe330Phe | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1063/6438 | 990/6174 | 330/2057 | chr2 | 96661763 | |||
chr2:96661781 | C | T | 1 | a0009c0025 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1008C>T | p.Asp336Asp | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1081/6438 | 1008/6174 | 336/2057 | chr2 | 96661781 | |||
chr2:96661790 | C | G | 1 | a0009c0025 | 1 | HG00099.hp1 | splice_region_variant&synonymous_variant | LOW | c.1017C>G | p.Leu339Leu | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/53 | 1090/6438 | 1017/6174 | 339/2057 | chr2 | 96661790 | |||
chr2:96668937 | C | T | 1 | a0001c0024 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1236C>T | p.Asn412Asn | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 16/53 | 1309/6438 | 1236/6174 | 412/2057 | chr2 | 96668937 | |||
chr2:96669095 | T | C | 1 | a0004c0013 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1320T>C | p.His440His | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 17/53 | 1393/6438 | 1320/6174 | 440/2057 | chr2 | 96669095 | |||
chr2:96686078 | G | A | 1 | a0002c0006 | 6 | HG02602.hp2 NA18612.hp2 NA18945.hp2 others(3): Show |
synonymous_variant | LOW | c.2034G>A | p.Ala678Ala | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 22/53 | 2107/6438 | 2034/6174 | 678/2057 | chr2 | 96686078 | |||
chr2:96689755 | C | T | 1 | a0001c0023 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.2637C>T | p.Asp879Asp | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/53 | 2710/6438 | 2637/6174 | 879/2057 | chr2 | 96689755 | |||
chr2:96693627 | A | G | 6 | a0001c0003 a0001c0004 a0001c0023 others(3): Show |
66 | HG00597.hp2 HG00642.hp2 HG01071.hp1 others(63): Show |
synonymous_variant | LOW | c.3414A>G | p.Pro1138Pro | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 32/53 | 3487/6438 | 3414/6174 | 1138/2057 | chr2 | 96693627 | |||
chr2:96699718 | C | T | 1 | a0001c0020 | 1 | NA18986.hp1 | splice_region_variant&synonymous_variant | LOW | c.4779C>T | p.Cys1593Cys | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 43/53 | 4852/6438 | 4779/6174 | 1593/2057 | chr2 | 96699718 | |||
chr2:96700351 | T | C | 1 | a0001c0004 | 25 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(22): Show |
synonymous_variant | LOW | c.4950T>C | p.Val1650Val | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/53 | 5023/6438 | 4950/6174 | 1650/2057 | chr2 | 96700351 | |||
chr2:96704338 | G | A | 1 | a0002c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.5925G>A | p.Leu1975Leu | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 52/53 | 5998/6438 | 5925/6174 | 1975/2057 | chr2 | 96704338 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96704790 | T | G | 1 | a0001c0002t0002 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 53/53 | 98 | chr2 | 96704790 | ||||||
chr2:96704867 | A | G | 1 | a0001c0003t0003 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 53/53 | 175 | chr2 | 96704867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96643445 | G | A | 1 | a0001c0004t0001g0002 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.85+524G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643445 | |||||||
chr2:96643512 | G | A | 1 | a0002c0001t0001g0003 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.85+591G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643512 | |||||||
chr2:96643513 | C | A | 1 | a0002c0001t0001g0003 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.85+592C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643513 | |||||||
chr2:96643538 | C | T | 3 | a0002c0001t0001g0223 a0002c0001t0001g0224 a0017c0014t0001g0225 |
3 | HG03130.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.85+617C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643538 | |||||||
chr2:96643639 | C | T | 4 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0222 others(1): Show |
4 | HG00558.hp2 HG00621.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+718C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643639 | |||||||
chr2:96643808 | G | T | 3 | a0001c0002t0001g0218 a0005c0007t0001g0217 a0006c0011t0001g0216 |
3 | HG01243.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.85+887G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643808 | |||||||
chr2:96643852 | A | G | 1 | a0002c0001t0001g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.85+931A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643852 | |||||||
chr2:96643959 | G | C | 37 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(34): Show |
37 | HG00558.hp2 HG00621.hp2 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.85+1038G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96643959 | |||||||
chr2:96644080 | G | A | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.85+1159G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644080 | |||||||
chr2:96644174 | C | CA | 28 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.85+1269dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr2 | 96644174 | ||||||
chr2:96644187 | A | G | 1 | a0002c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.85+1266A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644187 | |||||||
chr2:96644310 | C | T | 1 | a0001c0004t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.85+1389C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644310 | |||||||
chr2:96644322 | C | CA | 12 | a0001c0003t0001g0073 a0001c0004t0001g0038 a0002c0001t0001g0067 others(9): Show |
12 | HG00741.hp2 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.85+1413dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr2 | 96644322 | ||||||
chr2:96644357 | A | T | 1 | a0003c0005t0001g0212 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.85+1436A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644357 | |||||||
chr2:96644814 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.86-1587G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644814 | |||||||
chr2:96644816 | G | A | 2 | a0004c0012t0001g0004 a0004c0012t0001g0005 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.86-1585G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644816 | |||||||
chr2:96644957 | A | T | 1 | a0001c0002t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.86-1444A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96644957 | |||||||
chr2:96645220 | C | A | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.86-1181C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96645220 | |||||||
chr2:96645488 | C | T | 1 | a0001c0003t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.86-913C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96645488 | |||||||
chr2:96645516 | G | A | 1 | a0001c0003t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.86-885G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96645516 | |||||||
chr2:96645657 | C | T | 37 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.86-744C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96645657 | |||||||
chr2:96645784 | T | TCA | 50 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(47): Show |
50 | HG00558.hp2 HG00621.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.86-602_86-601dupCA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr2 | 96645784 | ||||||
chr2:96645996 | CT | C | 198 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0014 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.86-385delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr2 | 96645996 | ||||||
chr2:96646002 | T | C | 11 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0181 others(8): Show |
11 | HG00642.hp2 HG01358.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-399T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96646002 | |||||||
chr2:96646018 | T | A | 1 | a0001c0004t0001g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.86-383T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96646018 | |||||||
chr2:96646019 | G | C | 1 | a0001c0004t0001g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.86-382G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96646019 | |||||||
chr2:96646148 | G | A | 1 | a0016c0026t0001g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.86-253G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96646148 | |||||||
chr2:96646278 | G | A | 1 | a0001c0003t0001g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.86-123G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 1/52 | chr2 | 96646278 | |||||||
chr2:96646893 | C | T | 1 | a0001c0004t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-171C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 2/52 | chr2 | 96646893 | |||||||
chr2:96646908 | G | GCAAA | 6 | a0001c0003t0001g0006 a0001c0003t0001g0081 a0001c0003t0001g0082 others(3): Show |
6 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-154_139-151dup others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr2 | 96646908 | ||||||
chr2:96646914 | G | A | 1 | a0001c0004t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-150G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 2/52 | chr2 | 96646914 | |||||||
chr2:96646946 | G | A | 1 | a0001c0003t0001g0179 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-118G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 2/52 | chr2 | 96646946 | |||||||
chr2:96647013 | T | G | 1 | a0001c0004t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.139-51T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 2/52 | chr2 | 96647013 | |||||||
chr2:96647250 | A | C | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.230+95A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 3/52 | chr2 | 96647250 | |||||||
chr2:96647504 | C | T | 3 | a0001c0002t0001g0170 a0001c0004t0001g0168 a0001c0004t0001g0169 |
3 | HG01099.hp1 HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.231-274C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 3/52 | chr2 | 96647504 | |||||||
chr2:96647713 | C | G | 51 | a0001c0002t0001g0156 a0001c0002t0001g0164 a0001c0002t0001g0165 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.231-65C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 3/52 | chr2 | 96647713 | |||||||
chr2:96647714 | C | T | 35 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(32): Show |
35 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.231-64C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 3/52 | chr2 | 96647714 | |||||||
chr2:96647737 | C | A | 5 | a0001c0003t0001g0081 a0001c0003t0001g0082 a0001c0003t0001g0084 others(2): Show |
5 | HG02809.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-41C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 3/52 | chr2 | 96647737 | |||||||
chr2:96648373 | C | T | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.339+487C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | chr2 | 96648373 | |||||||
chr2:96648434 | G | GAAAGAAG others(25): Show |
1 | a0002c0001t0001g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.339+549_339+580dup others(32): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr2 | 96648434 | ||||||
chr2:96648438 | G | A | 38 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(35): Show |
38 | HG00558.hp2 HG00621.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.339+552G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | chr2 | 96648438 | |||||||
chr2:96648943 | A | G | 1 | a0002c0001t0001g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.340-680A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | chr2 | 96648943 | |||||||
chr2:96649039 | G | T | 1 | a0001c0002t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.340-584G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | chr2 | 96649039 | |||||||
chr2:96649190 | G | A | 2 | a0001c0002t0001g0187 a0001c0002t0001g0199 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.340-433G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 4/52 | chr2 | 96649190 | |||||||
chr2:96649709 | G | A | 2 | a0001c0002t0001g0187 a0001c0002t0001g0199 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.394+32G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 5/52 | chr2 | 96649709 | |||||||
chr2:96649833 | C | T | 48 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(45): Show |
48 | HG00099.hp2 HG00323.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.394+156C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 5/52 | chr2 | 96649833 | |||||||
chr2:96650455 | G | A | 1 | a0001c0003t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.504+166G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96650455 | |||||||
chr2:96650600 | T | C | 1 | a0003c0005t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.504+311T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96650600 | |||||||
chr2:96651237 | C | CTCTT | 27 | a0001c0002t0001g0117 a0001c0002t0001g0119 a0001c0002t0001g0120 others(24): Show |
27 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.505-594_505-591dup others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | C | CTCTTTCT others(1): Show |
9 | a0001c0002t0001g0040 a0001c0002t0001g0218 a0001c0003t0001g0196 others(6): Show |
9 | HG02723.hp1 HG02897.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-598_505-591dup others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | C | CTCTTTCT others(5): Show |
2 | a0001c0002t0001g0222 a0004c0012t0001g0005 |
2 | HG00621.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.505-602_505-591dup others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTT | C | 50 | a0001c0002t0001g0020 a0001c0002t0001g0103 a0001c0002t0001g0104 others(47): Show |
50 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.505-594_505-591del others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTTTCT others(1): Show |
C | 40 | a0001c0002t0001g0014 a0001c0002t0001g0017 a0001c0002t0001g0095 others(37): Show |
40 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.505-598_505-591del others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTTTCT others(5): Show |
C | 19 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0123 others(16): Show |
19 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.505-602_505-591del others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTTTCT others(9): Show |
C | 10 | a0001c0002t0001g0009 a0001c0002t0001g0086 a0001c0002t0001g0087 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.505-606_505-591del others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTTTCT others(13): Show |
C | 3 | a0001c0002t0001g0001 a0001c0002t0001g0085 a0001c0003t0001g0008 |
4 | HG01256.hp2 HG01258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-610_505-591del others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651237 | CTCTTTCT others(17): Show |
C | 1 | a0006c0011t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.505-614_505-591del others(24): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651237 | ||||||
chr2:96651248 | T | C | 2 | a0003c0005t0001g0076 a0003c0005t0001g0077 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.505-644T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651248 | |||||||
chr2:96651252 | T | C | 6 | a0001c0003t0001g0073 a0003c0005t0001g0068 a0003c0005t0001g0071 others(3): Show |
6 | HG02723.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-640T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651252 | |||||||
chr2:96651256 | T | C | 2 | a0003c0005t0001g0069 a0003c0005t0001g0070 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.505-636T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651256 | |||||||
chr2:96651303 | T | C | 1 | a0001c0002t0001g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.505-589T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651303 | |||||||
chr2:96651387 | TTTCCTTC others(30): Show |
T | 1 | a0001c0004t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.505-462_505-426del others(37): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651387 | ||||||
chr2:96651403 | CTTCT | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0012 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.505-474_505-471del others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | INFO_REALIGN_3_PRIME | chr2 | 96651403 | ||||||
chr2:96651630 | A | G | 10 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0181 others(7): Show |
10 | HG01358.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.505-262A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651630 | |||||||
chr2:96651883 | C | T | 1 | a0002c0001t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.505-9C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 6/52 | chr2 | 96651883 | |||||||
chr2:96652087 | G | A | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.633+67G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96652087 | |||||||
chr2:96652329 | T | C | 37 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.633+309T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96652329 | |||||||
chr2:96652482 | G | A | 37 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.633+462G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96652482 | |||||||
chr2:96652844 | T | C | 10 | a0001c0003t0001g0073 a0003c0005t0001g0068 a0003c0005t0001g0069 others(7): Show |
10 | HG02258.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-796T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96652844 | |||||||
chr2:96653046 | C | G | 1 | a0002c0001t0001g0161 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.634-594C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653046 | |||||||
chr2:96653079 | C | G | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.634-561C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653079 | |||||||
chr2:96653195 | C | G | 1 | a0003c0005t0001g0212 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.634-445C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653195 | |||||||
chr2:96653220 | C | A | 3 | a0001c0002t0001g0123 a0001c0004t0001g0047 a0001c0004t0001g0054 |
3 | HG01123.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.634-420C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653220 | |||||||
chr2:96653243 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.634-397C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653243 | |||||||
chr2:96653343 | A | C | 1 | a0001c0004t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.634-297A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653343 | |||||||
chr2:96653347 | GGAATATT others(17): Show |
G | 1 | a0007c0008t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.634-291_634-268del others(24): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr2 | 96653347 | ||||||
chr2:96653507 | T | C | 10 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0181 others(7): Show |
10 | HG01358.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-133T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 7/52 | chr2 | 96653507 | |||||||
chr2:96653797 | G | C | 50 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.696+95G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 8/52 | chr2 | 96653797 | |||||||
chr2:96653999 | T | C | 1 | a0001c0003t0001g0179 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.696+297T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 8/52 | chr2 | 96653999 | |||||||
chr2:96654172 | A | ACGTTGAG others(8): Show |
1 | a0001c0004t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.697-272_697-258dup others(15): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 8/52 | INFO_REALIGN_3_PRIME | chr2 | 96654172 | ||||||
chr2:96654289 | GAGTGAAA others(5): Show |
G | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.697-155_697-144del others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 8/52 | INFO_REALIGN_3_PRIME | chr2 | 96654289 | ||||||
chr2:96654301 | AACACCCA others(11): Show |
A | 1 | a0001c0002t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.697-144_697-127del others(18): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 8/52 | chr2 | 96654301 | |||||||
chr2:96654898 | C | CA | 50 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0020 others(47): Show |
50 | HG00558.hp2 HG00621.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.747+422dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96654898 | ||||||
chr2:96654898 | C | CAAAAAAA others(2649): Show |
1 | a0001c0002t0001g0188 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.747+419_747+420ins others(2656): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96654898 | ||||||
chr2:96654898 | CA | C | 8 | a0001c0002t0001g0211 a0001c0004t0001g0038 a0002c0001t0001g0041 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+422delA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96654898 | ||||||
chr2:96654916 | A | AG | 4 | a0001c0002t0001g0017 a0001c0003t0001g0008 a0001c0003t0001g0011 others(1): Show |
4 | HG02922.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+420_747+421ins others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96654916 | |||||||
chr2:96655000 | T | G | 183 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.747+504T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96655000 | |||||||
chr2:96655060 | TAACGTTT others(3): Show |
T | 1 | a0016c0026t0001g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.747+567_747+576del others(10): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96655060 | ||||||
chr2:96655573 | GACAGAGA others(4): Show |
G | 1 | a0008c0010t0001g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.747+1079_747+1089d others(13): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96655573 | ||||||
chr2:96655615 | G | A | 2 | a0001c0004t0001g0010 a0001c0004t0001g0012 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.747+1119G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96655615 | |||||||
chr2:96655726 | T | G | 1 | a0001c0003t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.747+1230T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96655726 | |||||||
chr2:96656013 | G | A | 2 | a0001c0002t0001g0187 a0001c0002t0001g0199 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.747+1517G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656013 | |||||||
chr2:96656102 | T | A | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+1606T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656102 | |||||||
chr2:96656125 | C | CCTTCACC others(17): Show |
1 | a0007c0008t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.747+1631_747+1654d others(26): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96656125 | ||||||
chr2:96656270 | A | G | 1 | a0002c0001t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.747+1774A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656270 | |||||||
chr2:96656290 | T | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+1794T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656290 | |||||||
chr2:96656366 | G | GTGGCTCA others(19): Show |
1 | a0002c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.747+1872_747+1897d others(28): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96656366 | ||||||
chr2:96656411 | C | T | 3 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0003g0083 |
3 | HG02809.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.747+1915C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656411 | |||||||
chr2:96656748 | CT | C | 14 | a0001c0002t0001g0027 a0001c0002t0001g0056 a0001c0002t0001g0085 others(11): Show |
14 | HG00323.hp2 HG01496.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.747+2268delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96656748 | ||||||
chr2:96656845 | T | A | 1 | a0004c0013t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.747+2349T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96656845 | |||||||
chr2:96656904 | TGAACCAA others(33): Show |
T | 1 | a0015c0015t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.747+2412_747+2451d others(42): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96656904 | ||||||
chr2:96657015 | A | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2519A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657015 | |||||||
chr2:96657017 | T | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2521T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657017 | |||||||
chr2:96657041 | G | GT | 4 | a0001c0002t0001g0115 a0001c0004t0001g0013 a0002c0001t0001g0130 others(1): Show |
4 | HG00558.hp1 NA18979.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+2552dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657041 | ||||||
chr2:96657065 | T | TTA | 62 | a0001c0002t0001g0056 a0001c0002t0001g0164 a0001c0002t0001g0165 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.747+2586_747+2587d others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657065 | ||||||
chr2:96657065 | T | TTATA | 4 | a0001c0002t0002g0094 a0001c0003t0001g0141 a0001c0004t0001g0007 others(1): Show |
4 | HG02622.hp1 HG03453.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+2584_747+2587d others(6): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657065 | ||||||
chr2:96657084 | G | T | 1 | a0002c0001t0001g0151 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.747+2588G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657084 | |||||||
chr2:96657215 | C | A | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2719C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657215 | |||||||
chr2:96657218 | G | A | 2 | a0001c0003t0001g0030 a0001c0004t0001g0024 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.747+2722G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657218 | |||||||
chr2:96657221 | C | T | 51 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.747+2725C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657221 | |||||||
chr2:96657276 | T | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2780T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657276 | |||||||
chr2:96657298 | C | A | 2 | a0002c0001t0001g0166 a0009c0025t0001g0153 |
2 | HG00099.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.747+2802C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657298 | |||||||
chr2:96657318 | G | C | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2822G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657318 | |||||||
chr2:96657375 | C | T | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2879C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657375 | |||||||
chr2:96657376 | T | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2880T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657376 | |||||||
chr2:96657377 | G | T | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.747+2881G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657377 | |||||||
chr2:96657459 | T | TA | 3 | a0001c0002t0001g0156 a0001c0004t0001g0013 a0002c0001t0001g0215 |
3 | NA19000.hp1 NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.748-2877dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657459 | ||||||
chr2:96657576 | TCCCATCC others(5): Show |
T | 1 | a0002c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.748-2762_748-2751d others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657576 | ||||||
chr2:96657798 | ATTGCTGA others(25): Show |
A | 1 | a0001c0002t0001g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.748-2541_748-2510d others(34): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96657798 | ||||||
chr2:96657939 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-2402G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96657939 | |||||||
chr2:96658012 | T | A | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.748-2329T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658012 | |||||||
chr2:96658020 | C | CT | 12 | a0001c0002t0001g0218 a0001c0003t0001g0023 a0001c0003t0001g0141 others(9): Show |
12 | HG01358.hp2 HG01943.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.748-2307dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658020 | ||||||
chr2:96658020 | CT | C | 7 | a0001c0002t0001g0039 a0001c0003t0001g0084 a0001c0004t0001g0168 others(4): Show |
7 | HG00558.hp1 HG01099.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-2307delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658020 | ||||||
chr2:96658086 | G | A | 1 | a0001c0003t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748-2255G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658086 | |||||||
chr2:96658204 | GACAGGTT others(6): Show |
G | 1 | a0010c0016t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.748-2135_748-2123d others(15): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658204 | ||||||
chr2:96658293 | T | TGCGTGAG others(17): Show |
1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.748-2047_748-2024d others(26): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658293 | ||||||
chr2:96658318 | C | CT | 40 | a0001c0002t0001g0091 a0001c0002t0001g0107 a0001c0002t0001g0119 others(37): Show |
40 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.748-2007dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658318 | ||||||
chr2:96658465 | C | T | 21 | a0001c0002t0001g0014 a0001c0002t0001g0027 a0001c0002t0001g0220 others(18): Show |
21 | HG00558.hp2 HG00621.hp2 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.748-1876C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658465 | |||||||
chr2:96658550 | A | G | 1 | a0002c0001t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.748-1791A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658550 | |||||||
chr2:96658561 | A | T | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-1780A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658561 | |||||||
chr2:96658564 | C | A | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-1777C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658564 | |||||||
chr2:96658565 | T | C | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-1776T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658565 | |||||||
chr2:96658595 | T | C | 1 | a0003c0005t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.748-1746T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658595 | |||||||
chr2:96658618 | C | G | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.748-1723C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658618 | |||||||
chr2:96658933 | GTTTTGT | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0003g0083 |
3 | HG02809.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.748-1385_748-1380d others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658933 | ||||||
chr2:96658954 | T | G | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-1387T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658954 | |||||||
chr2:96658956 | G | GT | 6 | a0001c0002t0001g0102 a0001c0004t0001g0059 a0002c0001t0001g0130 others(3): Show |
6 | HG00558.hp1 HG02486.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-1378dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96658956 | ||||||
chr2:96658971 | A | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748-1370A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96658971 | |||||||
chr2:96659004 | GGTGTGAT others(33): Show |
G | 1 | a0002c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.748-1336_748-1297d others(42): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659004 | |||||||
chr2:96659039 | G | T | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-1302G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659039 | |||||||
chr2:96659081 | A | G | 1 | a0001c0002t0001g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.748-1260A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659081 | |||||||
chr2:96659134 | C | T | 1 | a0002c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.748-1207C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659134 | |||||||
chr2:96659135 | G | A | 4 | a0001c0002t0001g0211 a0002c0001t0001g0124 a0002c0001t0001g0214 others(1): Show |
4 | HG02165.hp2 HG03834.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-1206G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659135 | |||||||
chr2:96659144 | A | T | 1 | a0002c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.748-1197A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659144 | |||||||
chr2:96659189 | TC | T | 3 | a0001c0002t0001g0110 a0001c0020t0001g0025 a0002c0001t0001g0130 |
3 | HG00558.hp1 NA18939.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.748-1149delC | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659189 | ||||||
chr2:96659236 | C | G | 1 | a0002c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.748-1105C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659236 | |||||||
chr2:96659254 | G | C | 48 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(45): Show |
48 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.748-1087G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659254 | |||||||
chr2:96659262 | C | T | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-1079C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659262 | |||||||
chr2:96659263 | A | C | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-1078A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659263 | |||||||
chr2:96659264 | T | A | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-1077T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659264 | |||||||
chr2:96659273 | A | T | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748-1068A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659273 | |||||||
chr2:96659288 | G | GCCTGCCT others(5): Show |
1 | a0001c0004t0001g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.748-1052_748-1051i others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659288 | ||||||
chr2:96659288 | G | GCTTTTCT others(103): Show |
1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1049_748-1048i others(112): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659288 | ||||||
chr2:96659288 | GCTTT | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0222 a0001c0004t0001g0024 |
3 | HG00621.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.748-1051_748-1048d others(6): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659288 | ||||||
chr2:96659290 | T | C | 36 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(33): Show |
36 | HG00558.hp2 HG01243.hp2 HG02155.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-1051T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659290 | |||||||
chr2:96659290 | T | TTTCCTTC others(7): Show |
1 | a0002c0001t0001g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.748-1043_748-1042i others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | T | TTTCCTTC others(5): Show |
2 | a0001c0002t0001g0102 a0001c0002t0001g0156 |
2 | HG02486.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.748-987_748-976dup others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | T | TTTCCTTC others(94): Show |
1 | a0002c0001t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.748-1004_748-1003i others(103): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(68): Show |
T | 1 | a0001c0003t0001g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.748-1048_748-974de others(76): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(72): Show |
T | 2 | a0001c0003t0001g0201 a0001c0003t0001g0203 |
2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.748-1048_748-970de others(80): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(76): Show |
T | 2 | a0001c0003t0001g0080 a0001c0003t0001g0207 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.748-1048_748-966de others(84): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(84): Show |
T | 2 | a0001c0003t0001g0200 a0001c0003t0001g0205 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.748-1048_748-958de others(92): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(88): Show |
T | 2 | a0001c0003t0001g0206 a0001c0003t0001g0208 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.748-1048_748-954de others(96): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(96): Show |
T | 2 | a0001c0002t0001g0191 a0001c0003t0001g0198 |
2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.748-1048_748-946de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(100): Show |
T | 2 | a0001c0003t0001g0197 a0003c0005t0001g0212 |
2 | HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.748-1048_748-942de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(104): Show |
T | 10 | a0001c0002t0001g0192 a0001c0002t0001g0209 a0001c0003t0001g0178 others(7): Show |
10 | HG00642.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.748-1048_748-938de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(108): Show |
T | 6 | a0001c0002t0001g0188 a0001c0003t0001g0179 a0002c0001t0001g0195 others(3): Show |
6 | HG02055.hp1 HG02300.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-1048_748-934de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(112): Show |
T | 1 | a0002c0001t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.748-1048_748-930de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659290 | TTTCCTTC others(124): Show |
T | 1 | a0001c0002t0001g0189 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.748-1048_748-918de others(1): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659290 | ||||||
chr2:96659291 | TTCCTTCC others(64): Show |
T | 1 | a0001c0003t0001g0204 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.748-1048_748-978de others(72): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659291 | ||||||
chr2:96659292 | T | G | 8 | a0001c0002t0001g0027 a0001c0002t0002g0094 a0001c0003t0001g0008 others(5): Show |
8 | HG01243.hp2 HG02155.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-1049T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659292 | |||||||
chr2:96659292 | T | TTCTTTCT others(111): Show |
1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1049_748-1048i others(120): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659292 | |||||||
chr2:96659293 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1048C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659293 | |||||||
chr2:96659294 | C | T | 1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1047C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659294 | |||||||
chr2:96659296 | T | C | 6 | a0001c0003t0001g0006 a0001c0003t0001g0081 a0001c0003t0001g0082 others(3): Show |
6 | HG02145.hp2 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.748-1045T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659296 | |||||||
chr2:96659296 | T | G | 2 | a0001c0002t0001g0027 a0002c0001t0001g0028 |
2 | HG02155.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.748-1045T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659296 | |||||||
chr2:96659297 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1044C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659297 | |||||||
chr2:96659298 | C | T | 1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1043C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659298 | |||||||
chr2:96659300 | T | G | 1 | a0002c0001t0001g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.748-1041T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659300 | |||||||
chr2:96659301 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1040C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659301 | |||||||
chr2:96659302 | C | T | 1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1039C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659302 | |||||||
chr2:96659305 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1036C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659305 | |||||||
chr2:96659306 | C | T | 1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1035C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659306 | |||||||
chr2:96659309 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.748-1032C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659309 | |||||||
chr2:96659310 | C | T | 1 | a0001c0003t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.748-1031C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659310 | |||||||
chr2:96659310 | CT | C | 2 | a0002c0001t0001g0158 a0002c0001t0001g0159 |
2 | HG01943.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.748-1029delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659310 | ||||||
chr2:96659314 | C | T | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1027C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659314 | |||||||
chr2:96659318 | C | T | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1023C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659318 | |||||||
chr2:96659322 | C | T | 3 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0006c0011t0001g0136 |
3 | HG01891.hp1 HG02165.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1019C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659322 | |||||||
chr2:96659326 | C | T | 3 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0006c0011t0001g0136 |
3 | HG01891.hp1 HG02165.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1015C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659326 | |||||||
chr2:96659327 | T | TTCCTTCC others(21): Show |
1 | a0001c0004t0001g0047 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.748-987_748-986ins others(28): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659327 | ||||||
chr2:96659330 | C | T | 3 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0006c0011t0001g0136 |
3 | HG01891.hp1 HG02165.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1011C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659330 | |||||||
chr2:96659333 | C | CCTTCCTT others(4): Show |
1 | a0001c0004t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.748-1006_748-996du others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659333 | ||||||
chr2:96659334 | C | CTTCCTTC others(66): Show |
1 | a0014c0021t0001g0146 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.748-996_748-995ins others(73): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659334 | ||||||
chr2:96659334 | C | T | 3 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0006c0011t0001g0136 |
3 | HG01891.hp1 HG02165.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.748-1007C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659334 | |||||||
chr2:96659337 | C | CTTCCTGT others(341): Show |
1 | a0015c0015t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.748-1004_748-1003i others(350): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659337 | |||||||
chr2:96659338 | C | T | 4 | a0001c0002t0001g0165 a0001c0003t0001g0078 a0001c0003t0001g0079 others(1): Show |
4 | HG00140.hp1 HG01891.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-1003C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659338 | |||||||
chr2:96659339 | T | TTCCTTCC others(13): Show |
1 | a0001c0004t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.748-983_748-982ins others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659339 | ||||||
chr2:96659341 | C | T | 1 | a0015c0015t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.748-1000C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659341 | |||||||
chr2:96659342 | C | CTTTCTTT others(155): Show |
1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.748-997_748-996ins others(162): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659342 | ||||||
chr2:96659342 | C | CTTTCTTT others(154): Show |
1 | a0001c0002t0001g0165 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.748-997_748-996ins others(161): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659342 | ||||||
chr2:96659342 | C | T | 11 | a0001c0003t0001g0078 a0001c0003t0001g0079 a0001c0004t0001g0108 others(8): Show |
11 | HG00597.hp2 HG01515.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-999C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659342 | |||||||
chr2:96659345 | C | T | 1 | a0015c0015t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.748-996C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659345 | |||||||
chr2:96659346 | C | CTTCTTTC others(314): Show |
1 | a0002c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.748-992_748-991ins others(321): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659346 | ||||||
chr2:96659346 | C | CTTTCTTC others(358): Show |
1 | a0002c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.748-993_748-992ins others(365): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659346 | ||||||
chr2:96659346 | C | CTTTCTTT others(199): Show |
1 | a0007c0008t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.748-993_748-992ins others(206): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659346 | ||||||
chr2:96659346 | C | CTTTCTTT others(107): Show |
1 | a0002c0001t0001g0147 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.748-993_748-992ins others(114): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659346 | ||||||
chr2:96659346 | C | T | 27 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.748-995C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659346 | |||||||
chr2:96659348 | T | C | 1 | a0002c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.748-993T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659348 | |||||||
chr2:96659349 | C | T | 3 | a0002c0001t0001g0037 a0002c0001t0001g0150 a0015c0015t0001g0135 |
3 | HG02698.hp2 HG03834.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.748-992C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659349 | |||||||
chr2:96659350 | C | CT | 9 | a0002c0001t0001g0130 a0002c0001t0001g0137 a0002c0001t0001g0145 others(6): Show |
9 | HG00558.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-989dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTCTTTC others(5): Show |
1 | a0001c0004t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.748-988_748-987ins others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(197): Show |
1 | a0001c0002t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.748-989_748-988ins others(204): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(303): Show |
1 | a0002c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.748-989_748-988ins others(310): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(203): Show |
1 | a0001c0004t0001g0002 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(210): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(279): Show |
1 | a0008c0010t0001g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(286): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(164): Show |
1 | a0002c0001t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(171): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(190): Show |
1 | a0002c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(197): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(198): Show |
1 | a0005c0007t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.748-989_748-988ins others(205): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(218): Show |
1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(225): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(238): Show |
1 | a0002c0001t0001g0175 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(245): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | CTTTCTTT others(278): Show |
1 | a0002c0001t0001g0003 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.748-989_748-988ins others(285): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | C | T | 22 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0003t0001g0078 others(19): Show |
22 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.748-991C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659350 | |||||||
chr2:96659350 | CTTCCTTC others(17): Show |
C | 1 | a0001c0003t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.748-987_748-964del others(24): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | CTTCCTTC others(25): Show |
C | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.748-987_748-956del others(32): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659350 | CTTCCTTC others(73): Show |
C | 1 | a0005c0007t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.748-987_748-908del others(80): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659350 | ||||||
chr2:96659353 | C | T | 3 | a0002c0001t0001g0037 a0008c0010t0001g0140 a0015c0015t0001g0135 |
3 | HG02698.hp2 NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.748-988C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659353 | |||||||
chr2:96659354 | C | CT | 3 | a0002c0001t0001g0142 a0002c0001t0001g0143 a0007c0008t0001g0133 |
3 | HG01975.hp2 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.748-985dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | CTTTCTTT others(152): Show |
1 | a0002c0001t0001g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.748-985_748-984ins others(159): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | CTTTCTTT others(179): Show |
1 | a0002c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.748-985_748-984ins others(186): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | CTTTCTTT others(321): Show |
1 | a0002c0001t0001g0152 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.748-985_748-984ins others(328): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | CTTTCTTT others(162): Show |
1 | a0002c0001t0001g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.748-985_748-984ins others(169): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | CTTTCTTT others(178): Show |
1 | a0002c0001t0001g0157 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.748-985_748-984ins others(185): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | C | T | 39 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(36): Show |
39 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.748-987C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659354 | |||||||
chr2:96659354 | CTTCCTTC others(13): Show |
C | 1 | a0002c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.748-983_748-964del others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659354 | CTTCCTTC others(57): Show |
C | 1 | a0002c0006t0001g0051 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.748-983_748-920del others(64): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659354 | ||||||
chr2:96659355 | T | TCTTCTCT others(238): Show |
1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.748-986_748-985ins others(245): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659355 | |||||||
chr2:96659355 | T | TTCTTTCT others(213): Show |
1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-984_748-983ins others(220): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659355 | ||||||
chr2:96659356 | T | TTCTTTCT others(51): Show |
1 | a0008c0010t0001g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.748-985_748-984ins others(58): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659356 | |||||||
chr2:96659357 | C | T | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.748-984C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659357 | |||||||
chr2:96659358 | C | CTTCTCCT others(105): Show |
1 | a0016c0026t0001g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.748-980_748-979ins others(112): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659358 | ||||||
chr2:96659358 | C | CTTCTTTC others(33): Show |
1 | a0001c0004t0001g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.748-980_748-979ins others(40): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659358 | ||||||
chr2:96659358 | C | CTTTCTTT others(380): Show |
1 | a0002c0001t0001g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.748-981_748-980ins others(387): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659358 | ||||||
chr2:96659358 | C | CTTTCTTT others(189): Show |
1 | a0001c0004t0001g0168 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.748-981_748-980ins others(196): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659358 | ||||||
chr2:96659358 | C | T | 50 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.748-983C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659358 | |||||||
chr2:96659361 | C | T | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.748-980C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659361 | |||||||
chr2:96659361 | CCTTCTTT others(6): Show |
C | 1 | a0001c0003t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.748-979_748-967del others(13): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659361 | |||||||
chr2:96659362 | C | CTTCCTTC others(150): Show |
1 | a0001c0002t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(157): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(157): Show |
1 | a0002c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(164): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(27): Show |
1 | a0001c0002t0001g0093 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(34): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(25): Show |
1 | a0001c0023t0001g0065 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(32): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(93): Show |
1 | a0001c0002t0001g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(100): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(148): Show |
1 | a0002c0001t0001g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(155): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(14): Show |
1 | a0001c0004t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(21): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(160): Show |
1 | a0001c0004t0001g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(167): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(21): Show |
1 | a0002c0001t0001g0114 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(28): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(5): Show |
1 | a0003c0005t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCCTTC others(21): Show |
1 | a0002c0001t0001g0026 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(28): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTCTTTC others(165): Show |
1 | a0002c0001t0001g0124 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.748-972_748-971ins others(172): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTTCTTT others(94): Show |
1 | a0002c0001t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.748-977_748-976ins others(101): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | CTTTCTTT others(282): Show |
1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.748-977_748-976ins others(289): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | C | T | 57 | a0001c0002t0001g0096 a0001c0002t0001g0164 a0001c0002t0001g0165 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.748-979C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659362 | |||||||
chr2:96659362 | CTTCTTTC others(1): Show |
C | 4 | a0001c0002t0001g0085 a0001c0002t0001g0089 a0001c0002t0001g0100 others(1): Show |
4 | HG00544.hp2 HG00642.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-839_748-832del others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(5): Show |
C | 5 | a0001c0002t0001g0001 a0001c0002t0001g0087 a0001c0002t0001g0091 others(2): Show |
5 | HG00621.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-843_748-832del others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(9): Show |
C | 2 | a0001c0002t0001g0103 a0001c0002t0001g0171 |
2 | HG01496.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.748-847_748-832del others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(13): Show |
C | 2 | a0001c0002t0001g0099 a0001c0002t0001g0120 |
2 | HG00639.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.748-851_748-832del others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(17): Show |
C | 2 | a0001c0002t0001g0097 a0002c0001t0001g0042 |
2 | HG00140.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.748-855_748-832del others(24): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(25): Show |
C | 2 | a0001c0002t0001g0112 a0002c0001t0001g0041 |
2 | HG00323.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.748-863_748-832del others(32): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(29): Show |
C | 3 | a0001c0002t0001g0101 a0001c0002t0001g0109 a0001c0002t0001g0117 |
3 | HG00673.hp2 HG01358.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.748-867_748-832del others(36): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(33): Show |
C | 1 | a0001c0003t0001g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.748-871_748-832del others(40): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(37): Show |
C | 1 | a0001c0003t0001g0082 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.748-875_748-832del others(44): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659362 | CTTCTTTC others(41): Show |
C | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-879_748-832del others(48): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659362 | ||||||
chr2:96659364 | T | C | 1 | a0002c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.748-977T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659364 | |||||||
chr2:96659364 | T | TCCTTCCT others(6): Show |
1 | a0002c0001t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(13): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659364 | ||||||
chr2:96659365 | C | CCTTCCTT others(78): Show |
1 | a0001c0020t0001g0025 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.748-976_748-975ins others(85): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659365 | |||||||
chr2:96659365 | C | CCTTCCTT others(40): Show |
1 | a0002c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.748-976_748-975ins others(47): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659365 | |||||||
chr2:96659365 | C | T | 1 | a0002c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.748-976C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659365 | |||||||
chr2:96659365 | CTTTCTTT others(14): Show |
C | 1 | a0001c0002t0001g0115 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.748-973_748-953del others(21): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659365 | ||||||
chr2:96659366 | T | A | 1 | a0001c0004t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.748-975T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659366 | |||||||
chr2:96659366 | T | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(64): Show |
67 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.748-975T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659366 | |||||||
chr2:96659369 | C | CCTTCCTT others(14): Show |
1 | a0010c0016t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.748-972_748-971ins others(21): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659369 | |||||||
chr2:96659369 | CTTTCTTT others(18): Show |
C | 1 | a0002c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-969_748-945del others(25): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659369 | ||||||
chr2:96659370 | T | C | 55 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(52): Show |
55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.748-971T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659370 | |||||||
chr2:96659370 | T | TTTCTTTC others(169): Show |
1 | a0002c0001t0001g0143 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.748-936_748-935ins others(176): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659370 | ||||||
chr2:96659371 | T | C | 1 | a0001c0004t0001g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.748-970T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659371 | |||||||
chr2:96659373 | CTTTCTTT others(6): Show |
C | 1 | a0001c0004t0001g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.748-965_748-953del others(13): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659373 | ||||||
chr2:96659373 | CTTTCTTT others(18): Show |
C | 1 | a0001c0003t0003g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.748-965_748-941del others(25): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659373 | ||||||
chr2:96659373 | CTTTCTTT others(26): Show |
C | 1 | a0002c0001t0001g0121 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.748-965_748-933del others(33): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659373 | ||||||
chr2:96659374 | T | C | 43 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(40): Show |
43 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.748-967T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659374 | |||||||
chr2:96659374 | T | TTTCCTTC others(48): Show |
1 | a0002c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.748-964_748-963ins others(55): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659374 | ||||||
chr2:96659374 | TTTCTTTC others(40): Show |
T | 1 | a0001c0002t0001g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.748-964_748-918del others(47): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659374 | ||||||
chr2:96659375 | TTCTTTCT others(11): Show |
T | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.748-964_748-947del others(18): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659375 | ||||||
chr2:96659378 | T | C | 33 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(30): Show |
34 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.748-963T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659378 | |||||||
chr2:96659379 | TTCTTTCT others(15): Show |
T | 1 | a0001c0002t0001g0098 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.748-960_748-939del others(22): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659379 | ||||||
chr2:96659380 | T | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748-961T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659380 | |||||||
chr2:96659381 | CT | C | 3 | a0001c0003t0001g0084 a0001c0004t0001g0013 a0002c0001t0001g0063 |
3 | HG01192.hp1 HG02809.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.748-957delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659381 | ||||||
chr2:96659381 | CTTTCTTT others(22): Show |
C | 1 | a0001c0002t0001g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.748-957_748-929del others(29): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659381 | ||||||
chr2:96659382 | T | C | 25 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(22): Show |
25 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.748-959T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659382 | |||||||
chr2:96659382 | T | TTTCTTTC others(189): Show |
1 | a0002c0001t0001g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.748-910_748-909ins others(196): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659382 | ||||||
chr2:96659382 | TTTCTTTC others(4): Show |
T | 1 | a0001c0003t0001g0023 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748-956_748-946del others(11): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659382 | ||||||
chr2:96659383 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.748-958T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659383 | |||||||
chr2:96659385 | C | T | 1 | a0001c0020t0001g0025 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.748-956C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659385 | |||||||
chr2:96659386 | T | C | 14 | a0001c0002t0001g0001 a0001c0002t0001g0087 a0001c0002t0001g0088 others(11): Show |
14 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.748-955T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659386 | |||||||
chr2:96659387 | T | C | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.748-954T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659387 | |||||||
chr2:96659388 | T | TCTTTCTT others(42): Show |
1 | a0002c0001t0001g0151 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.748-940_748-939ins others(49): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659388 | ||||||
chr2:96659390 | T | C | 12 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0089 others(9): Show |
12 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-951T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659390 | |||||||
chr2:96659391 | T | C | 3 | a0001c0003t0001g0202 a0001c0003t0001g0203 a0001c0003t0001g0204 |
3 | HG03130.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.748-950T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659391 | |||||||
chr2:96659393 | CTTTCTTT others(7): Show |
C | 1 | a0001c0002t0001g0088 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.748-946_748-933del others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659393 | ||||||
chr2:96659394 | T | C | 9 | a0001c0002t0001g0029 a0001c0002t0001g0087 a0001c0002t0001g0091 others(6): Show |
9 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-947T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659394 | |||||||
chr2:96659395 | T | C | 4 | a0001c0003t0001g0201 a0001c0003t0001g0202 a0001c0003t0001g0203 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-946T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659395 | |||||||
chr2:96659396 | T | C | 1 | a0002c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.748-945T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659396 | |||||||
chr2:96659396 | T | TTCTTTCT others(270): Show |
1 | a0002c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.748-945_748-944ins others(277): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659396 | |||||||
chr2:96659397 | C | CTTTCTTT others(41): Show |
1 | a0001c0004t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.748-918_748-917ins others(48): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659397 | ||||||
chr2:96659397 | C | T | 1 | a0002c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.748-944C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659397 | |||||||
chr2:96659398 | T | C | 8 | a0001c0002t0001g0087 a0001c0002t0001g0091 a0001c0002t0001g0097 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-943T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659398 | |||||||
chr2:96659399 | T | C | 6 | a0001c0003t0001g0080 a0001c0003t0001g0201 a0001c0003t0001g0202 others(3): Show |
6 | HG02257.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-942T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659399 | |||||||
chr2:96659402 | T | C | 7 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0101 others(4): Show |
7 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-939T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659402 | |||||||
chr2:96659403 | T | C | 8 | a0001c0003t0001g0080 a0001c0003t0001g0200 a0001c0003t0001g0201 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-938T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659403 | |||||||
chr2:96659404 | T | TCCTTTCC others(64): Show |
1 | a0002c0001t0001g0137 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.748-936_748-935ins others(71): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659404 | ||||||
chr2:96659404 | T | TCTTCCTT others(101): Show |
1 | a0001c0004t0001g0108 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.748-934_748-933ins others(108): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659404 | ||||||
chr2:96659406 | T | C | 5 | a0001c0002t0001g0097 a0001c0002t0001g0101 a0001c0002t0001g0117 others(2): Show |
5 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-935T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659406 | |||||||
chr2:96659407 | T | C | 9 | a0001c0003t0001g0080 a0001c0003t0001g0200 a0001c0003t0001g0201 others(6): Show |
9 | HG01884.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-934T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659407 | |||||||
chr2:96659408 | T | C | 2 | a0001c0003t0001g0081 a0002c0001t0001g0137 |
2 | HG03098.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.748-933T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659408 | |||||||
chr2:96659409 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.748-932C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659409 | |||||||
chr2:96659410 | T | A | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.748-931T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659410 | |||||||
chr2:96659410 | T | C | 2 | a0001c0003t0001g0082 a0002c0001t0001g0041 |
2 | HG00323.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.748-931T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659410 | |||||||
chr2:96659411 | T | C | 10 | a0001c0003t0001g0080 a0001c0003t0001g0200 a0001c0003t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-930T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659411 | |||||||
chr2:96659412 | T | C | 1 | a0002c0001t0001g0137 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.748-929T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659412 | |||||||
chr2:96659414 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-927T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659414 | |||||||
chr2:96659415 | T | C | 12 | a0001c0002t0001g0191 a0001c0003t0001g0080 a0001c0003t0001g0198 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-926T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659415 | |||||||
chr2:96659415 | TTCTTTCT others(7): Show |
T | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.748-924_748-911del others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659415 | ||||||
chr2:96659416 | T | C | 1 | a0002c0001t0001g0137 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.748-925T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659416 | |||||||
chr2:96659416 | T | TCCTTCCT others(62): Show |
1 | a0002c0001t0001g0176 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.748-924_748-923ins others(69): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659416 | ||||||
chr2:96659417 | C | CTTCTTTC others(65): Show |
1 | a0002c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.748-922_748-921ins others(72): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659417 | ||||||
chr2:96659418 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-923T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659418 | |||||||
chr2:96659418 | TTTCTTTC others(16): Show |
T | 1 | a0001c0002t0001g0106 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.748-920_748-898del others(23): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659418 | ||||||
chr2:96659419 | T | C | 13 | a0001c0002t0001g0191 a0001c0003t0001g0080 a0001c0003t0001g0198 others(10): Show |
13 | HG01358.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.748-922T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659419 | |||||||
chr2:96659420 | T | C | 2 | a0002c0001t0001g0137 a0002c0001t0001g0176 |
2 | NA18963.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.748-921T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659420 | |||||||
chr2:96659421 | CTT | C | 4 | a0001c0002t0001g0192 a0001c0002t0001g0209 a0001c0003t0001g0185 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-918_748-917del others(2): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659421 | ||||||
chr2:96659422 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-919T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659422 | |||||||
chr2:96659422 | TTTCTTTC others(8): Show |
T | 1 | a0017c0014t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.748-916_748-902del others(15): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659422 | ||||||
chr2:96659423 | T | C | 21 | a0001c0002t0001g0086 a0001c0002t0001g0191 a0001c0003t0001g0080 others(18): Show |
21 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.748-918T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659423 | |||||||
chr2:96659424 | T | C | 2 | a0002c0001t0001g0137 a0002c0001t0001g0176 |
2 | NA18963.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.748-917T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659424 | |||||||
chr2:96659426 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.748-915T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659426 | |||||||
chr2:96659427 | T | C | 28 | a0001c0002t0001g0191 a0001c0002t0001g0192 a0001c0002t0001g0209 others(25): Show |
28 | HG00642.hp2 HG01358.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.748-914T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659427 | |||||||
chr2:96659428 | T | C | 1 | a0002c0001t0001g0176 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.748-913T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659428 | |||||||
chr2:96659429 | C | T | 1 | a0002c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-912C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659429 | |||||||
chr2:96659430 | T | C | 2 | a0001c0002t0001g0110 a0002c0001t0001g0090 |
2 | HG02258.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.748-911T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659430 | |||||||
chr2:96659430 | T | G | 1 | a0002c0006t0001g0048 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.748-911T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659430 | |||||||
chr2:96659430 | TTTCTTTC others(4): Show |
T | 1 | a0001c0004t0001g0118 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.748-908_748-898del others(11): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659430 | ||||||
chr2:96659431 | T | C | 31 | a0001c0002t0001g0188 a0001c0002t0001g0191 a0001c0002t0001g0192 others(28): Show |
31 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-910T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659431 | |||||||
chr2:96659431 | T | TTCTTTCT others(268): Show |
1 | a0002c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.748-893_748-892ins others(275): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659431 | ||||||
chr2:96659432 | T | C | 1 | a0001c0002t0001g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.748-909T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659432 | |||||||
chr2:96659434 | T | G | 1 | a0002c0006t0001g0049 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.748-907T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659434 | |||||||
chr2:96659435 | T | C | 30 | a0001c0002t0001g0188 a0001c0002t0001g0191 a0001c0002t0001g0192 others(27): Show |
30 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.748-906T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659435 | |||||||
chr2:96659438 | T | TTCTTTCT others(3): Show |
1 | a0002c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.748-902_748-901ins others(10): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659438 | ||||||
chr2:96659439 | T | C | 31 | a0001c0002t0001g0188 a0001c0002t0001g0191 a0001c0002t0001g0192 others(28): Show |
31 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.748-902T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659439 | |||||||
chr2:96659442 | T | G | 1 | a0002c0006t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.748-899T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659442 | |||||||
chr2:96659443 | T | C | 28 | a0001c0002t0001g0188 a0001c0002t0001g0191 a0001c0002t0001g0192 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.748-898T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659443 | |||||||
chr2:96659444 | T | C | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-897T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659444 | |||||||
chr2:96659445 | C | T | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-896C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659445 | |||||||
chr2:96659446 | T | G | 1 | a0002c0006t0001g0043 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.748-895T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659446 | |||||||
chr2:96659447 | T | C | 27 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(24): Show |
27 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.748-894T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659447 | |||||||
chr2:96659449 | CTTTCTTT others(55): Show |
C | 1 | a0002c0006t0001g0048 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.748-891_748-830del others(62): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659449 | |||||||
chr2:96659451 | T | C | 23 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(20): Show |
23 | HG00642.hp2 HG01081.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.748-890T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659451 | |||||||
chr2:96659453 | C | CTTTCTTT others(14): Show |
1 | a0001c0004t0001g0033 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.748-885_748-865dup others(21): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659453 | ||||||
chr2:96659453 | C | CTTTCTTT others(15): Show |
1 | a0002c0001t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.748-886_748-865dup others(22): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659453 | ||||||
chr2:96659453 | CT | C | 3 | a0001c0002t0001g0110 a0001c0002t0001g0191 a0002c0001t0001g0158 |
3 | HG02970.hp2 NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.748-885delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659453 | ||||||
chr2:96659453 | CTTTCTTT others(51): Show |
C | 1 | a0002c0006t0001g0049 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.748-887_748-830del others(58): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659453 | |||||||
chr2:96659455 | T | C | 17 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0192 others(14): Show |
17 | HG00642.hp2 HG01081.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.748-886T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659455 | |||||||
chr2:96659457 | C | CTTTCTTT others(15): Show |
1 | a0002c0001t0001g0145 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.748-882_748-861dup others(22): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659457 | ||||||
chr2:96659459 | T | C | 11 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0192 others(8): Show |
11 | HG00642.hp2 HG01081.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.748-882T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659459 | |||||||
chr2:96659461 | CT | C | 3 | a0002c0001t0001g0159 a0002c0001t0001g0160 a0015c0015t0001g0135 |
3 | HG01943.hp1 HG04184.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.748-877delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659461 | ||||||
chr2:96659461 | CTTTCTTT others(43): Show |
C | 1 | a0002c0006t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.748-879_748-830del others(50): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659461 | |||||||
chr2:96659463 | T | C | 6 | a0001c0002t0001g0189 a0001c0003t0001g0197 a0001c0003t0001g0198 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-878T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659463 | |||||||
chr2:96659465 | CTTTCTTT others(39): Show |
C | 2 | a0001c0002t0001g0199 a0002c0006t0001g0043 |
2 | HG03453.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.748-875_748-830del others(46): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659465 | |||||||
chr2:96659467 | T | C | 3 | a0001c0002t0001g0189 a0002c0001t0001g0194 a0002c0001t0001g0195 |
3 | HG01081.hp1 HG02300.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.748-874T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659467 | |||||||
chr2:96659470 | T | C | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.748-871T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659470 | |||||||
chr2:96659474 | T | C | 1 | a0008c0010t0001g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.748-867T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659474 | |||||||
chr2:96659477 | CTTTCTTT others(27): Show |
C | 3 | a0001c0002t0001g0009 a0001c0003t0001g0011 a0001c0003t0001g0030 |
3 | HG02976.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.748-863_748-830del others(34): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659477 | |||||||
chr2:96659478 | T | C | 1 | a0002c0001t0001g0158 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.748-863T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659478 | |||||||
chr2:96659478 | TTTCTTTC others(16): Show |
T | 1 | a0004c0012t0001g0005 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-860_748-838del others(23): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659478 | ||||||
chr2:96659480 | T | C | 1 | a0005c0007t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.748-861T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659480 | |||||||
chr2:96659481 | CTTTCTTT others(23): Show |
C | 2 | a0001c0003t0001g0062 a0001c0003t0001g0196 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.748-859_748-830del others(30): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659481 | |||||||
chr2:96659485 | CTTTCTTT others(19): Show |
C | 6 | a0001c0002t0001g0123 a0001c0002t0002g0094 a0001c0003t0001g0008 others(3): Show |
6 | HG01243.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.748-855_748-830del others(26): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659485 | |||||||
chr2:96659489 | CTTTCTTT others(15): Show |
C | 4 | a0002c0001t0001g0063 a0002c0001t0001g0224 a0003c0005t0001g0074 others(1): Show |
4 | HG01192.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-851_748-830del others(22): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659489 | |||||||
chr2:96659490 | T | G | 1 | a0002c0006t0001g0051 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.748-851T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659490 | |||||||
chr2:96659493 | CTTTCTTT others(11): Show |
C | 5 | a0001c0003t0001g0073 a0001c0004t0001g0010 a0002c0001t0001g0131 others(2): Show |
5 | HG01255.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-847_748-830del others(18): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659493 | |||||||
chr2:96659497 | CTTTCTTT others(7): Show |
C | 3 | a0003c0005t0001g0069 a0003c0005t0001g0076 a0003c0005t0001g0077 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.748-843_748-830del others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659497 | |||||||
chr2:96659498 | T | C | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.748-843T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659498 | |||||||
chr2:96659501 | CTTTCTTT others(3): Show |
C | 3 | a0001c0002t0001g0017 a0001c0004t0001g0024 a0004c0013t0001g0019 |
3 | HG02717.hp1 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.748-839_748-830del others(10): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659501 | |||||||
chr2:96659505 | CTTTCGA | C | 9 | a0001c0002t0001g0020 a0001c0002t0001g0027 a0001c0002t0001g0040 others(6): Show |
9 | HG00323.hp2 HG02723.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-835_748-830del others(6): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659505 | |||||||
chr2:96659509 | C | CTT | 3 | a0001c0004t0001g0007 a0003c0005t0001g0068 a0014c0021t0001g0146 |
3 | NA18962.hp2 NA18970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.748-832_748-831ins others(2): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(49): Show |
1 | a0001c0004t0001g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(56): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(246): Show |
1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(253): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(104): Show |
1 | a0001c0003t0001g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(111): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(196): Show |
1 | a0002c0001t0001g0167 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(203): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(83): Show |
1 | a0006c0011t0001g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.748-832_748-831ins others(90): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(91): Show |
1 | a0005c0007t0001g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(98): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(128): Show |
1 | a0002c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(135): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(230): Show |
1 | a0007c0008t0001g0133 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.748-832_748-831ins others(237): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(245): Show |
1 | a0002c0001t0001g0161 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.748-832_748-831ins others(252): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(215): Show |
1 | a0001c0004t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(222): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | CTTTCTTT others(238): Show |
1 | a0002c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.748-832_748-831ins others(245): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | C | T | 1 | a0003c0005t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.748-832C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659509 | |||||||
chr2:96659509 | CGA | C | 110 | a0001c0002t0001g0014 a0001c0002t0001g0029 a0001c0002t0001g0039 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.748-829_748-828del others(2): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659509 | ||||||
chr2:96659510 | G | T | 17 | a0001c0003t0001g0141 a0001c0004t0001g0007 a0001c0004t0001g0022 others(14): Show |
17 | HG00558.hp1 HG01975.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.748-831G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659510 | |||||||
chr2:96659511 | A | C | 16 | a0001c0003t0001g0141 a0001c0004t0001g0007 a0001c0004t0001g0036 others(13): Show |
16 | HG00558.hp1 HG01975.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-830A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659511 | |||||||
chr2:96659511 | A | T | 1 | a0001c0004t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.748-830A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659511 | |||||||
chr2:96659512 | G | A | 4 | a0001c0003t0001g0062 a0002c0001t0001g0223 a0002c0001t0001g0224 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-829G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659512 | |||||||
chr2:96659559 | T | G | 1 | a0002c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-782T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659559 | |||||||
chr2:96659587 | G | T | 1 | a0001c0004t0001g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.748-754G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659587 | |||||||
chr2:96659610 | A | C | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-731A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659610 | |||||||
chr2:96659627 | G | A | 47 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.748-714G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659627 | |||||||
chr2:96659627 | G | C | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.748-714G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659627 | |||||||
chr2:96659633 | AG | A | 3 | a0001c0002t0001g0110 a0002c0001t0001g0155 a0016c0026t0001g0219 |
3 | NA18939.hp2 NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.748-704delG | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659633 | ||||||
chr2:96659637 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0066 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.748-704G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659637 | |||||||
chr2:96659637 | G | GC | 6 | a0001c0004t0001g0015 a0001c0004t0001g0018 a0002c0001t0001g0063 others(3): Show |
6 | HG00558.hp1 HG01192.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.748-701dupC | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659637 | ||||||
chr2:96659646 | C | CA | 2 | a0001c0003t0001g0023 a0002c0001t0001g0161 |
2 | NA18966.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.748-694dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659646 | ||||||
chr2:96659649 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.748-692G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659649 | |||||||
chr2:96659668 | T | A | 1 | a0001c0003t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.748-673T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659668 | |||||||
chr2:96659680 | A | C | 1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-661A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659680 | |||||||
chr2:96659682 | A | C | 1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-659A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659682 | |||||||
chr2:96659709 | T | TC | 3 | a0001c0002t0001g0098 a0001c0002t0001g0106 a0001c0002t0001g0156 |
3 | HG01975.hp1 HG01993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.748-631dupC | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96659709 | ||||||
chr2:96659729 | G | A | 24 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(21): Show |
24 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.748-612G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659729 | |||||||
chr2:96659942 | A | G | 1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-399A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659942 | |||||||
chr2:96659983 | C | A | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.748-358C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96659983 | |||||||
chr2:96660024 | T | C | 1 | a0002c0001t0001g0161 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.748-317T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96660024 | |||||||
chr2:96660034 | C | A | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748-307C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96660034 | |||||||
chr2:96660035 | A | G | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748-306A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96660035 | |||||||
chr2:96660087 | GT | G | 2 | a0002c0001t0001g0090 a0002c0001t0001g0158 |
2 | HG02258.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.748-252delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | INFO_REALIGN_3_PRIME | chr2 | 96660087 | ||||||
chr2:96660252 | C | A | 1 | a0001c0004t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.748-89C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 9/52 | chr2 | 96660252 | |||||||
chr2:96660409 | G | GA | 3 | a0001c0002t0001g0110 a0001c0002t0001g0156 a0002c0001t0001g0215 |
3 | NA18939.hp2 NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.778+43dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | INFO_REALIGN_3_PRIME | chr2 | 96660409 | ||||||
chr2:96660446 | C | G | 3 | a0001c0003t0001g0141 a0005c0007t0001g0138 a0005c0007t0001g0139 |
3 | HG02145.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.778+75C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660446 | |||||||
chr2:96660450 | A | T | 1 | a0001c0003t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778+79A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660450 | |||||||
chr2:96660548 | AT | A | 4 | a0001c0002t0001g0103 a0001c0003t0001g0081 a0001c0004t0001g0066 others(1): Show |
4 | HG02155.hp1 HG02257.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+183delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | INFO_REALIGN_3_PRIME | chr2 | 96660548 | ||||||
chr2:96660549 | T | C | 49 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.778+178T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660549 | |||||||
chr2:96660567 | T | A | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.778+196T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660567 | |||||||
chr2:96660660 | T | A | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.778+289T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660660 | |||||||
chr2:96660846 | A | G | 1 | a0001c0003t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.778+475A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660846 | |||||||
chr2:96660944 | A | T | 1 | a0002c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.779-381A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660944 | |||||||
chr2:96660952 | AT | A | 3 | a0001c0004t0001g0169 a0002c0001t0001g0037 a0002c0001t0001g0158 |
3 | HG01099.hp1 HG02698.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.779-367delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | INFO_REALIGN_3_PRIME | chr2 | 96660952 | ||||||
chr2:96660972 | G | A | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.779-353G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96660972 | |||||||
chr2:96661133 | A | T | 1 | a0002c0001t0001g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.779-192A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96661133 | |||||||
chr2:96661168 | G | A | 1 | a0002c0001t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.779-157G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 10/52 | chr2 | 96661168 | |||||||
chr2:96661451 | C | T | 1 | a0002c0001t0001g0121 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.894+11C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 11/52 | chr2 | 96661451 | |||||||
chr2:96661523 | A | G | 1 | a0001c0003t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.894+83A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 11/52 | chr2 | 96661523 | |||||||
chr2:96661792 | G | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | splice_donor_variant&intron_variant | HIGH | c.1018+1G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661792 | |||||||
chr2:96661798 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.1018+7G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661798 | |||||||
chr2:96661800 | C | G | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+9C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661800 | |||||||
chr2:96661802 | G | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+11G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661802 | |||||||
chr2:96661803 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+12G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661803 | |||||||
chr2:96661804 | G | C | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+13G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661804 | |||||||
chr2:96661805 | T | TATTAAAT others(4): Show |
1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+14_1018+15ins others(11): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661805 | |||||||
chr2:96661806 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+15G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661806 | |||||||
chr2:96661807 | C | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+16C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661807 | |||||||
chr2:96661811 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+20G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661811 | |||||||
chr2:96661812 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+21G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661812 | |||||||
chr2:96661814 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+23G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661814 | |||||||
chr2:96661815 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+24G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661815 | |||||||
chr2:96661818 | G | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+27G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661818 | |||||||
chr2:96661819 | C | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+28C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661819 | |||||||
chr2:96661820 | A | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+29A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661820 | |||||||
chr2:96661821 | G | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+30G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661821 | |||||||
chr2:96661822 | C | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+31C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661822 | |||||||
chr2:96661823 | C | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+32C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661823 | |||||||
chr2:96661824 | C | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+33C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661824 | |||||||
chr2:96661827 | A | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+36A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661827 | |||||||
chr2:96661831 | T | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+40T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661831 | |||||||
chr2:96661832 | C | G | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+41C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661832 | |||||||
chr2:96661833 | C | A | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+42C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661833 | |||||||
chr2:96661834 | C | T | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1018+43C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661834 | |||||||
chr2:96661984 | C | T | 31 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(28): Show |
31 | HG02155.hp2 HG02717.hp1 HG02809.hp2 others(28): Show |
intron_variant | MODIFIER | c.1018+193C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96661984 | |||||||
chr2:96662045 | C | T | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1019-170C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96662045 | |||||||
chr2:96662094 | T | A | 1 | a0001c0002t0001g0165 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1019-121T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96662094 | |||||||
chr2:96662152 | A | C | 1 | a0001c0002t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1019-63A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 12/52 | chr2 | 96662152 | |||||||
chr2:96662354 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1071+87A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662354 | |||||||
chr2:96662421 | C | T | 1 | a0002c0001t0001g0143 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1071+154C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662421 | |||||||
chr2:96662461 | A | C | 1 | a0001c0002t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1071+194A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662461 | |||||||
chr2:96662589 | A | G | 34 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1071+322A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662589 | |||||||
chr2:96662649 | A | G | 1 | a0004c0009t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1071+382A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662649 | |||||||
chr2:96662777 | C | G | 1 | a0001c0003t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1071+510C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662777 | |||||||
chr2:96662784 | A | T | 1 | a0001c0002t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1071+517A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96662784 | |||||||
chr2:96663016 | C | CACAGATA others(5): Show |
1 | a0001c0002t0001g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1072-422_1072-411d others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr2 | 96663016 | ||||||
chr2:96663115 | C | T | 157 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1072-324C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96663115 | |||||||
chr2:96663137 | A | G | 54 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(51): Show |
54 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1072-302A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 13/52 | chr2 | 96663137 | |||||||
chr2:96663674 | C | G | 17 | a0001c0002t0001g0014 a0001c0002t0001g0027 a0001c0004t0001g0007 others(14): Show |
17 | HG02155.hp2 HG03017.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.1140+167C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96663674 | |||||||
chr2:96663844 | A | G | 1 | a0002c0001t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1140+337A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96663844 | |||||||
chr2:96663932 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1140+425A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96663932 | |||||||
chr2:96664170 | G | C | 1 | a0001c0002t0001g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1140+663G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664170 | |||||||
chr2:96664291 | A | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0084 a0001c0003t0003g0083 |
3 | HG02809.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1140+784A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664291 | |||||||
chr2:96664321 | G | A | 8 | a0001c0004t0001g0108 a0002c0001t0001g0067 a0002c0001t0001g0132 others(5): Show |
8 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1140+814G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664321 | |||||||
chr2:96664353 | C | A | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1140+846C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664353 | |||||||
chr2:96664610 | G | A | 3 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0091 |
3 | HG01069.hp2 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1140+1103G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664610 | |||||||
chr2:96664635 | G | A | 1 | a0014c0021t0001g0146 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1140+1128G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664635 | |||||||
chr2:96664695 | T | C | 1 | a0001c0004t0001g0168 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1140+1188T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664695 | |||||||
chr2:96664904 | G | A | 1 | a0002c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1140+1397G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664904 | |||||||
chr2:96664951 | A | T | 1 | a0001c0003t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1140+1444A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96664951 | |||||||
chr2:96665125 | A | G | 1 | a0003c0005t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1140+1618A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96665125 | |||||||
chr2:96665517 | A | G | 4 | a0001c0003t0001g0081 a0001c0003t0001g0082 a0001c0003t0001g0084 others(1): Show |
4 | HG02809.hp1 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+2010A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96665517 | |||||||
chr2:96665848 | A | G | 42 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(39): Show |
42 | HG00558.hp2 HG00621.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1140+2341A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96665848 | |||||||
chr2:96665937 | T | C | 1 | a0001c0003t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1140+2430T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96665937 | |||||||
chr2:96666254 | C | A | 1 | a0006c0011t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1141-2497C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96666254 | |||||||
chr2:96666659 | A | T | 3 | a0001c0003t0001g0081 a0001c0003t0001g0082 a0001c0003t0003g0083 |
3 | HG03098.hp2 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1141-2092A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96666659 | |||||||
chr2:96666659 | AT | A | 7 | a0001c0002t0001g0189 a0002c0001t0001g0067 a0002c0001t0001g0132 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1141-2080delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | INFO_REALIGN_3_PRIME | chr2 | 96666659 | ||||||
chr2:96666663 | T | A | 6 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0003t0001g0205 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141-2088T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96666663 | |||||||
chr2:96666707 | G | A | 1 | a0001c0004t0001g0033 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1141-2044G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96666707 | |||||||
chr2:96667065 | G | C | 10 | a0001c0003t0001g0073 a0003c0005t0001g0068 a0003c0005t0001g0069 others(7): Show |
10 | HG02258.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1141-1686G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667065 | |||||||
chr2:96667139 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1141-1612G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667139 | |||||||
chr2:96667347 | C | CT | 7 | a0001c0003t0001g0200 a0002c0001t0001g0003 a0002c0001t0001g0063 others(4): Show |
7 | HG00544.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1141-1387dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | INFO_REALIGN_3_PRIME | chr2 | 96667347 | ||||||
chr2:96667347 | CT | C | 7 | a0001c0002t0001g0027 a0001c0002t0001g0089 a0001c0002t0001g0189 others(4): Show |
7 | HG00741.hp2 HG01943.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141-1387delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | INFO_REALIGN_3_PRIME | chr2 | 96667347 | ||||||
chr2:96667470 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1141-1281C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667470 | |||||||
chr2:96667489 | A | C | 1 | a0001c0002t0001g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1141-1262A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667489 | |||||||
chr2:96667505 | A | C | 1 | a0001c0004t0001g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1141-1246A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667505 | |||||||
chr2:96667579 | T | G | 24 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(21): Show |
24 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1141-1172T>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667579 | |||||||
chr2:96667755 | A | C | 2 | a0002c0001t0001g0041 a0002c0001t0001g0042 |
2 | HG00323.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1141-996A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96667755 | |||||||
chr2:96667863 | CT | C | 14 | a0001c0002t0001g0014 a0001c0002t0001g0027 a0001c0004t0001g0013 others(11): Show |
14 | HG02155.hp2 HG03017.hp2 HG03669.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-880delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | INFO_REALIGN_3_PRIME | chr2 | 96667863 | ||||||
chr2:96668135 | A | G | 6 | a0002c0001t0001g0067 a0002c0001t0001g0132 a0002c0001t0001g0142 others(3): Show |
6 | HG00639.hp2 HG00741.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1141-616A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96668135 | |||||||
chr2:96668176 | C | T | 1 | a0001c0002t0001g0039 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1141-575C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96668176 | |||||||
chr2:96668361 | C | CA | 39 | a0001c0002t0001g0104 a0001c0002t0001g0123 a0001c0002t0001g0188 others(36): Show |
39 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.1141-377dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | INFO_REALIGN_3_PRIME | chr2 | 96668361 | ||||||
chr2:96668667 | G | A | 1 | a0002c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1141-84G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 14/52 | chr2 | 96668667 | |||||||
chr2:96669533 | G | A | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1362+396G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 17/52 | chr2 | 96669533 | |||||||
chr2:96669773 | T | C | 37 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(34): Show |
37 | HG01243.hp2 HG02145.hp2 HG02155.hp2 others(34): Show |
intron_variant | MODIFIER | c.1363-346T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 17/52 | chr2 | 96669773 | |||||||
chr2:96669801 | A | T | 1 | a0001c0002t0001g0112 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1363-318A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 17/52 | chr2 | 96669801 | |||||||
chr2:96669899 | T | C | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1363-220T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 17/52 | chr2 | 96669899 | |||||||
chr2:96670352 | G | C | 35 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(32): Show |
35 | HG01243.hp2 HG02155.hp2 HG02717.hp1 others(32): Show |
intron_variant | MODIFIER | c.1491+105G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96670352 | |||||||
chr2:96670384 | G | A | 1 | a0002c0006t0001g0048 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1491+137G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96670384 | |||||||
chr2:96670543 | C | T | 13 | a0001c0002t0001g0107 a0001c0002t0001g0109 a0001c0002t0001g0111 others(10): Show |
13 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1491+296C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96670543 | |||||||
chr2:96670982 | C | T | 1 | a0002c0001t0001g0026 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1491+735C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96670982 | |||||||
chr2:96671106 | C | CA | 7 | a0001c0002t0001g0107 a0001c0002t0001g0120 a0001c0002t0001g0222 others(4): Show |
7 | HG00597.hp1 HG00621.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1491+881dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(3): Show |
34 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0004t0001g0002 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1491+872_1491+881d others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(4): Show |
8 | a0001c0002t0001g0170 a0002c0001t0001g0037 a0002c0001t0001g0145 others(5): Show |
8 | HG01123.hp2 HG02280.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1491+871_1491+881d others(13): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(5): Show |
5 | a0001c0003t0001g0141 a0002c0001t0001g0152 a0002c0001t0001g0161 others(2): Show |
5 | HG02622.hp1 HG03486.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1491+870_1491+881d others(14): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(6): Show |
13 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(10): Show |
13 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1491+869_1491+881d others(15): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(7): Show |
29 | a0001c0002t0001g0056 a0001c0002t0001g0187 a0001c0002t0001g0192 others(26): Show |
29 | HG00323.hp1 HG00323.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.1491+868_1491+881d others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(8): Show |
29 | a0001c0002t0001g0017 a0001c0002t0001g0039 a0001c0002t0001g0040 others(26): Show |
29 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1491+867_1491+881d others(17): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(9): Show |
25 | a0001c0002t0001g0014 a0001c0002t0001g0020 a0001c0002t0001g0029 others(22): Show |
25 | HG01192.hp1 HG02040.hp1 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.1491+866_1491+881d others(18): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(10): Show |
17 | a0001c0002t0001g0009 a0001c0003t0001g0006 a0001c0003t0001g0023 others(14): Show |
17 | HG01891.hp1 HG02155.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1491+865_1491+881d others(19): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(11): Show |
6 | a0001c0002t0001g0027 a0003c0005t0001g0070 a0003c0005t0001g0071 others(3): Show |
6 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+864_1491+881d others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(12): Show |
4 | a0003c0005t0001g0068 a0003c0005t0001g0072 a0003c0005t0001g0074 others(1): Show |
4 | HG02970.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1491+863_1491+881d others(21): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671106 | C | CAAAAAAA others(16): Show |
1 | a0003c0005t0001g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1491+881_1491+882i others(25): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96671106 | ||||||
chr2:96671150 | G | A | 1 | a0001c0004t0001g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1491+903G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671150 | |||||||
chr2:96671242 | C | G | 102 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1491+995C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671242 | |||||||
chr2:96671489 | A | C | 1 | a0001c0002t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1491+1242A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671489 | |||||||
chr2:96671754 | G | T | 42 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(39): Show |
42 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1492-1323G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671754 | |||||||
chr2:96671920 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1492-1157G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671920 | |||||||
chr2:96671944 | G | C | 3 | a0002c0001t0001g0144 a0002c0001t0001g0158 a0002c0001t0001g0214 |
3 | NA18939.hp1 NA18947.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1492-1133G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96671944 | |||||||
chr2:96672389 | T | C | 35 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(32): Show |
35 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.1492-688T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96672389 | |||||||
chr2:96672552 | C | A | 1 | a0005c0007t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1492-525C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96672552 | |||||||
chr2:96672614 | C | G | 1 | a0001c0002t0001g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1492-463C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96672614 | |||||||
chr2:96672660 | A | ATG | 66 | a0001c0002t0001g0014 a0001c0002t0001g0039 a0001c0002t0001g0040 others(63): Show |
66 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1492-391_1492-390d others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96672660 | ||||||
chr2:96672660 | A | ATGTG | 13 | a0001c0002t0001g0056 a0001c0002t0001g0218 a0002c0001t0001g0041 others(10): Show |
13 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.1492-393_1492-390d others(6): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr2 | 96672660 | ||||||
chr2:96673003 | T | C | 10 | a0001c0003t0001g0080 a0001c0003t0001g0200 a0001c0003t0001g0201 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492-74T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 18/52 | chr2 | 96673003 | |||||||
chr2:96673342 | A | G | 1 | a0004c0009t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1669+88A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96673342 | |||||||
chr2:96673418 | C | CTG | 179 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1669+165_1669+166i others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96673418 | ||||||
chr2:96673541 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1669+287T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96673541 | |||||||
chr2:96673710 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1669+456A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96673710 | |||||||
chr2:96674036 | A | G | 1 | a0001c0004t0001g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1669+782A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674036 | |||||||
chr2:96674044 | T | C | 179 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1669+790T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674044 | |||||||
chr2:96674297 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1669+1043A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674297 | |||||||
chr2:96674586 | T | C | 1 | a0001c0003t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1669+1332T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674586 | |||||||
chr2:96674613 | T | C | 2 | a0001c0002t0001g0119 a0001c0002t0001g0156 |
2 | HG00544.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1669+1359T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674613 | |||||||
chr2:96674693 | T | C | 6 | a0001c0002t0001g0009 a0001c0002t0001g0020 a0001c0002t0001g0029 others(3): Show |
6 | HG02896.hp1 HG02897.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1669+1439T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674693 | |||||||
chr2:96674730 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0066 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1669+1476G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96674730 | |||||||
chr2:96675026 | G | A | 42 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0056 others(39): Show |
42 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1669+1772G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675026 | |||||||
chr2:96675075 | T | C | 1 | a0001c0002t0001g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1669+1821T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675075 | |||||||
chr2:96675332 | C | G | 1 | a0004c0009t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1669+2078C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675332 | |||||||
chr2:96675415 | T | A | 1 | a0003c0005t0001g0212 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1669+2161T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675415 | |||||||
chr2:96675482 | A | C | 1 | a0008c0010t0001g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1669+2228A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675482 | |||||||
chr2:96675587 | C | T | 47 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1669+2333C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96675587 | |||||||
chr2:96676043 | TG | T | 8 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(5): Show |
8 | HG01081.hp1 HG01496.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1669+2790delG | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676043 | |||||||
chr2:96676288 | C | T | 2 | a0001c0002t0001g0056 a0002c0001t0001g0052 |
2 | HG00323.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1669+3034C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676288 | |||||||
chr2:96676453 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1669+3199C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676453 | |||||||
chr2:96676578 | C | G | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1669+3324C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676578 | |||||||
chr2:96676631 | G | GT | 6 | a0001c0003t0001g0080 a0001c0003t0001g0186 a0001c0004t0001g0059 others(3): Show |
6 | HG00741.hp2 HG01192.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1669+3392dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96676631 | ||||||
chr2:96676683 | G | C | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1669+3429G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676683 | |||||||
chr2:96676736 | A | C | 1 | a0009c0025t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1669+3482A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676736 | |||||||
chr2:96676870 | T | A | 33 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0191 others(30): Show |
33 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.1669+3616T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96676870 | |||||||
chr2:96677084 | C | T | 1 | a0002c0006t0001g0048 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1669+3830C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677084 | |||||||
chr2:96677130 | C | T | 1 | a0002c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1669+3876C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677130 | |||||||
chr2:96677238 | T | C | 1 | a0001c0003t0001g0198 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1669+3984T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677238 | |||||||
chr2:96677275 | C | T | 142 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(139): Show |
142 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1669+4021C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677275 | |||||||
chr2:96677288 | C | G | 1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1669+4034C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677288 | |||||||
chr2:96677566 | G | A | 32 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(29): Show |
32 | HG01243.hp2 HG02155.hp2 HG02717.hp1 others(29): Show |
intron_variant | MODIFIER | c.1669+4312G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677566 | |||||||
chr2:96677593 | C | T | 1 | a0001c0004t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1669+4339C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677593 | |||||||
chr2:96677594 | G | T | 49 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1669+4340G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96677594 | |||||||
chr2:96677865 | CA | C | 5 | a0001c0002t0001g0027 a0001c0002t0001g0218 a0001c0004t0001g0013 others(2): Show |
5 | HG00544.hp1 HG03516.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1669+4626delA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96677865 | ||||||
chr2:96678102 | CT | C | 22 | a0001c0002t0001g0187 a0001c0002t0001g0199 a0001c0002t0001g0211 others(19): Show |
22 | HG01256.hp1 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1669+4859delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96678102 | ||||||
chr2:96678156 | G | A | 50 | a0001c0002t0001g0164 a0001c0002t0001g0165 a0001c0002t0001g0170 others(47): Show |
50 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1669+4902G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678156 | |||||||
chr2:96678593 | T | C | 1 | a0002c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1669+5339T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678593 | |||||||
chr2:96678617 | G | C | 1 | a0002c0001t0001g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1669+5363G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678617 | |||||||
chr2:96678677 | C | T | 1 | a0002c0001t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1669+5423C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678677 | |||||||
chr2:96678918 | C | T | 1 | a0002c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1670-5409C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678918 | |||||||
chr2:96678984 | C | G | 1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1670-5343C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96678984 | |||||||
chr2:96679177 | C | G | 1 | a0001c0003t0001g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1670-5150C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679177 | |||||||
chr2:96679210 | T | C | 1 | a0002c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1670-5117T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679210 | |||||||
chr2:96679217 | A | G | 1 | a0001c0004t0001g0168 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1670-5110A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679217 | |||||||
chr2:96679228 | G | GTT | 35 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0020 others(32): Show |
35 | HG01243.hp2 HG02145.hp2 HG02155.hp2 others(32): Show |
intron_variant | MODIFIER | c.1670-5086_1670-508 others(6): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96679228 | ||||||
chr2:96679251 | G | A | 3 | a0002c0001t0001g0144 a0002c0001t0001g0158 a0002c0001t0001g0214 |
3 | NA18939.hp1 NA18947.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1670-5076G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679251 | |||||||
chr2:96679368 | C | T | 1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1670-4959C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679368 | |||||||
chr2:96679391 | T | C | 1 | a0005c0007t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1670-4936T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679391 | |||||||
chr2:96679488 | C | T | 10 | a0001c0003t0001g0073 a0003c0005t0001g0068 a0003c0005t0001g0069 others(7): Show |
10 | HG02258.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1670-4839C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679488 | |||||||
chr2:96679502 | G | A | 2 | a0002c0001t0001g0037 a0002c0001t0001g0127 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1670-4825G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679502 | |||||||
chr2:96679514 | A | G | 2 | a0001c0002t0001g0165 a0002c0001t0001g0166 |
2 | HG00140.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1670-4813A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679514 | |||||||
chr2:96679518 | G | A | 1 | a0004c0013t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1670-4809G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679518 | |||||||
chr2:96679870 | C | T | 2 | a0002c0001t0001g0137 a0002c0001t0001g0176 |
2 | NA18963.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1670-4457C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679870 | |||||||
chr2:96679940 | C | T | 2 | a0001c0003t0001g0008 a0001c0003t0001g0011 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1670-4387C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96679940 | |||||||
chr2:96680004 | T | C | 9 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0184 others(6): Show |
9 | HG01358.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1670-4323T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680004 | |||||||
chr2:96680079 | G | A | 10 | a0001c0003t0001g0073 a0003c0005t0001g0068 a0003c0005t0001g0069 others(7): Show |
10 | HG02258.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1670-4248G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680079 | |||||||
chr2:96680087 | C | A | 1 | a0002c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1670-4240C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680087 | |||||||
chr2:96680137 | A | G | 2 | a0001c0003t0001g0008 a0001c0003t0001g0011 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1670-4190A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680137 | |||||||
chr2:96680282 | A | G | 4 | a0002c0001t0001g0044 a0002c0001t0001g0053 a0002c0001t0001g0055 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670-4045A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680282 | |||||||
chr2:96680335 | T | C | 1 | a0001c0003t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1670-3992T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680335 | |||||||
chr2:96680408 | C | T | 1 | a0001c0003t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1670-3919C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680408 | |||||||
chr2:96680461 | A | T | 6 | a0001c0004t0001g0015 a0001c0004t0001g0022 a0001c0004t0001g0036 others(3): Show |
6 | HG04184.hp2 NA18942.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1670-3866A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680461 | |||||||
chr2:96680597 | A | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0020 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1670-3730A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680597 | |||||||
chr2:96680598 | T | C | 98 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0020 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1670-3729T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680598 | |||||||
chr2:96680666 | G | A | 36 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0020 others(33): Show |
36 | HG00642.hp2 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.1670-3661G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680666 | |||||||
chr2:96680739 | T | C | 2 | a0001c0003t0001g0185 a0004c0009t0001g0125 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1670-3588T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96680739 | |||||||
chr2:96681037 | A | T | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1670-3290A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681037 | |||||||
chr2:96681131 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0020 a0001c0002t0001g0029 others(6): Show |
9 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1670-3196C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681131 | |||||||
chr2:96681226 | T | C | 1 | a0002c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1670-3101T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681226 | |||||||
chr2:96681231 | G | A | 1 | a0001c0004t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1670-3096G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681231 | |||||||
chr2:96681274 | G | A | 1 | a0006c0011t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1670-3053G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681274 | |||||||
chr2:96681275 | G | A | 1 | a0001c0020t0001g0025 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1670-3052G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681275 | |||||||
chr2:96681289 | A | G | 12 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0003c0005t0001g0068 others(9): Show |
12 | HG01891.hp2 HG02258.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1670-3038A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681289 | |||||||
chr2:96681305 | C | A | 1 | a0001c0003t0001g0185 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1670-3022C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681305 | |||||||
chr2:96681313 | T | C | 31 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0209 others(28): Show |
31 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1670-3014T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681313 | |||||||
chr2:96681444 | C | G | 8 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0184 others(5): Show |
8 | HG01358.hp2 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1670-2883C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681444 | |||||||
chr2:96681546 | T | A | 3 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0015c0015t0001g0135 |
3 | HG02723.hp1 NA18986.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1670-2781T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681546 | |||||||
chr2:96681605 | T | C | 10 | a0003c0005t0001g0068 a0003c0005t0001g0069 a0003c0005t0001g0070 others(7): Show |
10 | HG02258.hp2 HG02895.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1670-2722T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681605 | |||||||
chr2:96681772 | T | TTTTA | 22 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0101 others(19): Show |
22 | HG01358.hp1 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1670-2523_1670-252 others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681772 | T | TTTTATTT others(1): Show |
19 | a0001c0002t0001g0089 a0001c0002t0001g0095 a0001c0002t0001g0096 others(16): Show |
19 | HG00642.hp1 HG00673.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1670-2527_1670-252 others(12): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681772 | T | TTTTATTT others(5): Show |
30 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(27): Show |
31 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1670-2531_1670-252 others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681772 | T | TTTTATTT others(9): Show |
2 | a0001c0002t0001g0105 a0001c0020t0001g0025 |
2 | NA18950.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1670-2535_1670-252 others(20): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681772 | T | TTTTATTT others(13): Show |
1 | a0001c0002t0001g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1670-2539_1670-252 others(24): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681772 | TTTTA | T | 50 | a0001c0003t0001g0008 a0001c0003t0001g0011 a0001c0003t0001g0030 others(47): Show |
50 | HG00597.hp2 HG00642.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1670-2523_1670-252 others(8): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr2 | 96681772 | ||||||
chr2:96681900 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1670-2427C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681900 | |||||||
chr2:96681975 | G | A | 2 | a0001c0002t0001g0218 a0001c0003t0001g0179 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1670-2352G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96681975 | |||||||
chr2:96682105 | G | A | 1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1670-2222G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96682105 | |||||||
chr2:96682579 | T | C | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1670-1748T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96682579 | |||||||
chr2:96682732 | G | A | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1670-1595G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96682732 | |||||||
chr2:96682757 | A | G | 7 | a0001c0003t0001g0008 a0001c0003t0001g0011 a0001c0003t0001g0081 others(4): Show |
7 | HG01884.hp2 HG02809.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1670-1570A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96682757 | |||||||
chr2:96683116 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1670-1211G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683116 | |||||||
chr2:96683125 | G | A | 2 | a0005c0007t0001g0138 a0005c0007t0001g0139 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1670-1202G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683125 | |||||||
chr2:96683268 | C | T | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1670-1059C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683268 | |||||||
chr2:96683554 | G | A | 1 | a0005c0007t0001g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1670-773G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683554 | |||||||
chr2:96683566 | C | G | 1 | a0001c0003t0001g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1670-761C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683566 | |||||||
chr2:96683578 | C | G | 14 | a0001c0002t0001g0001 a0001c0002t0001g0056 a0001c0002t0001g0085 others(11): Show |
15 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1670-749C>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96683578 | |||||||
chr2:96684216 | A | G | 26 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(23): Show |
26 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1670-111A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 19/52 | chr2 | 96684216 | |||||||
chr2:96684492 | C | T | 3 | a0002c0001t0001g0058 a0002c0001t0001g0147 a0002c0001t0001g0163 |
3 | HG00099.hp2 HG01258.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1794+41C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 20/52 | chr2 | 96684492 | |||||||
chr2:96684748 | G | T | 1 | a0002c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1794+297G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 20/52 | chr2 | 96684748 | |||||||
chr2:96684996 | CCTGTTGG others(7): Show |
C | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1795-332_1795-319d others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 20/52 | chr2 | 96684996 | |||||||
chr2:96685296 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1795-33G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 20/52 | chr2 | 96685296 | |||||||
chr2:96685613 | C | T | 2 | a0001c0002t0002g0094 a0001c0003t0001g0141 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1895+184C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 21/52 | chr2 | 96685613 | |||||||
chr2:96685651 | C | T | 1 | a0002c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1895+222C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 21/52 | chr2 | 96685651 | |||||||
chr2:96685824 | A | G | 76 | a0001c0002t0002g0094 a0001c0003t0001g0006 a0001c0003t0001g0008 others(73): Show |
76 | HG00597.hp2 HG00642.hp2 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.1896-116A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 21/52 | chr2 | 96685824 | |||||||
chr2:96685894 | G | C | 6 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0185 others(3): Show |
6 | HG01358.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1896-46G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 21/52 | chr2 | 96685894 | |||||||
chr2:96685916 | C | T | 2 | a0001c0003t0001g0184 a0001c0003t0001g0210 |
2 | HG00642.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1896-24C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 21/52 | chr2 | 96685916 | |||||||
chr2:96686149 | G | T | 1 | a0001c0004t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2073+32G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 22/52 | chr2 | 96686149 | |||||||
chr2:96686593 | A | T | 1 | a0010c0016t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2229+243A>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96686593 | |||||||
chr2:96686672 | T | A | 135 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(132): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.2229+322T>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96686672 | |||||||
chr2:96686855 | C | CA | 36 | a0001c0002t0001g0104 a0001c0002t0001g0115 a0001c0002t0001g0156 others(33): Show |
36 | HG00597.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.2229+529dupA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | INFO_REALIGN_3_PRIME | chr2 | 96686855 | ||||||
chr2:96686855 | CA | C | 28 | a0001c0002t0001g0027 a0001c0002t0001g0189 a0001c0003t0001g0030 others(25): Show |
28 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.2229+529delA | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | INFO_REALIGN_3_PRIME | chr2 | 96686855 | ||||||
chr2:96686881 | A | C | 1 | a0001c0002t0001g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2229+531A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96686881 | |||||||
chr2:96686890 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2229+540A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96686890 | |||||||
chr2:96686956 | C | T | 40 | a0001c0003t0001g0023 a0001c0003t0001g0030 a0001c0004t0001g0002 others(37): Show |
40 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.2229+606C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96686956 | |||||||
chr2:96687178 | C | T | 13 | a0001c0002t0001g0009 a0001c0002t0001g0020 a0001c0002t0001g0029 others(10): Show |
13 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2230-638C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687178 | |||||||
chr2:96687205 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2230-611G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687205 | |||||||
chr2:96687306 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2230-510G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687306 | |||||||
chr2:96687323 | A | C | 26 | a0001c0002t0002g0094 a0001c0003t0001g0006 a0001c0003t0001g0008 others(23): Show |
26 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2230-493A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687323 | |||||||
chr2:96687511 | C | T | 1 | a0001c0003t0001g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2230-305C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687511 | |||||||
chr2:96687650 | G | A | 3 | a0001c0003t0001g0184 a0001c0003t0001g0205 a0001c0003t0001g0210 |
3 | HG00642.hp2 HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2230-166G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687650 | |||||||
chr2:96687706 | C | T | 2 | a0001c0004t0001g0010 a0001c0004t0001g0012 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2230-110C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | chr2 | 96687706 | |||||||
chr2:96687723 | G | GGGGAA | 52 | a0001c0003t0001g0023 a0001c0003t0001g0030 a0001c0003t0001g0073 others(49): Show |
52 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.2230-89_2230-85dup others(5): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 23/52 | INFO_REALIGN_3_PRIME | chr2 | 96687723 | ||||||
chr2:96687988 | G | A | 52 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0017 others(49): Show |
53 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.2361+41G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96687988 | |||||||
chr2:96688070 | A | G | 1 | a0002c0001t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2361+123A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688070 | |||||||
chr2:96688076 | C | T | 1 | a0006c0011t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2361+129C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688076 | |||||||
chr2:96688151 | T | C | 11 | a0001c0003t0001g0073 a0001c0003t0001g0080 a0001c0003t0001g0200 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2361+204T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688151 | |||||||
chr2:96688276 | C | T | 1 | a0015c0015t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2361+329C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688276 | |||||||
chr2:96688357 | C | T | 1 | a0001c0002t0001g0112 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2361+410C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688357 | |||||||
chr2:96688586 | G | A | 7 | a0001c0003t0001g0008 a0001c0003t0001g0011 a0001c0003t0001g0081 others(4): Show |
7 | HG01884.hp2 HG02809.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2362-627G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688586 | |||||||
chr2:96688593 | T | C | 1 | a0001c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2362-620T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96688593 | |||||||
chr2:96689008 | C | T | 5 | a0002c0006t0001g0032 a0002c0006t0001g0048 a0002c0006t0001g0049 others(2): Show |
5 | HG02602.hp2 NA18612.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2362-205C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 24/52 | chr2 | 96689008 | |||||||
chr2:96689386 | G | C | 1 | a0002c0017t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2525+10G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 25/52 | chr2 | 96689386 | |||||||
chr2:96689861 | C | A | 1 | a0002c0001t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2640+103C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/52 | chr2 | 96689861 | |||||||
chr2:96689876 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0011 a0001c0003t0001g0030 others(8): Show |
11 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2640+118G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/52 | chr2 | 96689876 | |||||||
chr2:96690111 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0185 others(1): Show |
4 | HG02615.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2640+353C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/52 | chr2 | 96690111 | |||||||
chr2:96690133 | A | G | 2 | a0002c0001t0001g0067 a0002c0001t0001g0132 |
2 | HG00741.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2641-354A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/52 | chr2 | 96690133 | |||||||
chr2:96690466 | G | A | 4 | a0001c0003t0001g0030 a0001c0003t0001g0184 a0001c0003t0001g0205 others(1): Show |
4 | HG00642.hp2 HG01884.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2641-21G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 26/52 | chr2 | 96690466 | |||||||
chr2:96690608 | G | A | 1 | a0013c0019t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2743+19G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 27/52 | chr2 | 96690608 | |||||||
chr2:96690612 | G | A | 1 | a0002c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2743+23G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 27/52 | chr2 | 96690612 | |||||||
chr2:96690728 | G | T | 3 | a0001c0003t0001g0062 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2743+139G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 27/52 | chr2 | 96690728 | |||||||
chr2:96690730 | C | A | 1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2743+141C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 27/52 | chr2 | 96690730 | |||||||
chr2:96690737 | G | A | 1 | a0001c0003t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2743+148G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 27/52 | chr2 | 96690737 | |||||||
chr2:96691371 | G | A | 26 | a0001c0004t0001g0002 a0001c0004t0001g0007 a0001c0004t0001g0010 others(23): Show |
26 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.2907+18G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 28/52 | chr2 | 96691371 | |||||||
chr2:96691824 | G | A | 1 | a0001c0002t0001g0009 | 1 | NA21309.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.3076-1G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 29/52 | chr2 | 96691824 | |||||||
chr2:96692014 | G | A | 2 | a0006c0011t0001g0136 a0006c0011t0001g0216 |
2 | HG01243.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.3214+51G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 30/52 | chr2 | 96692014 | |||||||
chr2:96692019 | C | CG | 58 | a0001c0002t0001g0017 a0001c0002t0001g0095 a0001c0002t0001g0100 others(55): Show |
58 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.3214+67dupG | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 30/52 | INFO_REALIGN_3_PRIME | chr2 | 96692019 | ||||||
chr2:96692024 | G | C | 2 | a0001c0002t0001g0001 a0001c0002t0001g0085 |
3 | HG01256.hp2 HG01258.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3214+61G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 30/52 | chr2 | 96692024 | |||||||
chr2:96692186 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.3292+5G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692186 | |||||||
chr2:96692267 | C | A | 1 | a0001c0003t0001g0023 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3292+86C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692267 | |||||||
chr2:96692701 | G | A | 1 | a0001c0003t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3292+520G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692701 | |||||||
chr2:96692932 | C | T | 1 | a0001c0002t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3293-574C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692932 | |||||||
chr2:96692959 | C | T | 1 | a0001c0003t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3293-547C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692959 | |||||||
chr2:96692981 | G | T | 4 | a0001c0002t0001g0103 a0001c0002t0001g0188 a0001c0002t0001g0211 others(1): Show |
4 | HG03834.hp1 NA18970.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3293-525G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96692981 | |||||||
chr2:96693045 | G | A | 1 | a0001c0003t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3293-461G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693045 | |||||||
chr2:96693048 | C | T | 1 | a0002c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3293-458C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693048 | |||||||
chr2:96693124 | C | T | 1 | a0001c0002t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3293-382C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693124 | |||||||
chr2:96693153 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3293-353C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693153 | |||||||
chr2:96693189 | A | G | 4 | a0001c0003t0001g0008 a0001c0003t0001g0011 a0001c0003t0001g0082 others(1): Show |
4 | HG01884.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3293-317A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693189 | |||||||
chr2:96693327 | C | A | 1 | a0005c0007t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3293-179C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693327 | |||||||
chr2:96693432 | G | T | 1 | a0002c0001t0001g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3293-74G>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693432 | |||||||
chr2:96693475 | G | C | 1 | a0001c0004t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3293-31G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693475 | |||||||
chr2:96693499 | C | A | 37 | a0001c0003t0001g0073 a0001c0003t0001g0080 a0001c0003t0001g0196 others(34): Show |
37 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(34): Show |
splice_region_variant&intron_variant | LOW | c.3293-7C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 31/52 | chr2 | 96693499 | |||||||
chr2:96693705 | G | C | 3 | a0002c0001t0001g0058 a0002c0001t0001g0147 a0002c0001t0001g0163 |
3 | HG00099.hp2 HG01258.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3474+18G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 32/52 | chr2 | 96693705 | |||||||
chr2:96693802 | C | T | 22 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(19): Show |
22 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3475-109C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 32/52 | chr2 | 96693802 | |||||||
chr2:96694342 | C | T | 51 | a0001c0002t0001g0014 a0001c0002t0001g0017 a0001c0002t0001g0027 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.3637-18C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 33/52 | chr2 | 96694342 | |||||||
chr2:96694618 | G | A | 1 | a0003c0005t0001g0074 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3741+154G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96694618 | |||||||
chr2:96694995 | G | C | 1 | a0001c0003t0001g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3742-514G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96694995 | |||||||
chr2:96695014 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3742-495G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96695014 | |||||||
chr2:96695059 | A | C | 3 | a0001c0003t0001g0062 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3742-450A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96695059 | |||||||
chr2:96695356 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3742-153C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96695356 | |||||||
chr2:96695391 | C | A | 1 | a0001c0002t0001g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3742-118C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 34/52 | chr2 | 96695391 | |||||||
chr2:96696441 | C | A | 2 | a0002c0001t0001g0067 a0002c0001t0001g0132 |
2 | HG00741.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.4083+364C>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696441 | |||||||
chr2:96696588 | C | T | 1 | a0001c0002t0001g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4083+511C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696588 | |||||||
chr2:96696613 | T | C | 3 | a0001c0003t0001g0141 a0001c0003t0001g0197 a0001c0003t0001g0198 |
3 | HG01891.hp2 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4083+536T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696613 | |||||||
chr2:96696774 | G | A | 4 | a0001c0002t0001g0218 a0005c0007t0001g0138 a0005c0007t0001g0139 others(1): Show |
4 | HG02145.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4083+697G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696774 | |||||||
chr2:96696806 | G | A | 21 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(18): Show |
21 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4084-720G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696806 | |||||||
chr2:96696810 | C | T | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4084-716C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696810 | |||||||
chr2:96696954 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4084-572G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96696954 | |||||||
chr2:96697092 | C | T | 11 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(8): Show |
11 | HG00642.hp2 HG01884.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.4084-434C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | chr2 | 96697092 | |||||||
chr2:96697279 | TTCCAGAA others(7): Show |
T | 1 | a0001c0004t0001g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4084-227_4084-214d others(16): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr2 | 96697279 | ||||||
chr2:96697630 | C | T | 1 | a0002c0017t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4135-30C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 38/52 | chr2 | 96697630 | |||||||
chr2:96697932 | G | A | 1 | a0006c0011t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4237-105G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 39/52 | chr2 | 96697932 | |||||||
chr2:96698359 | G | C | 1 | a0001c0002t0001g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4356+203G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 40/52 | chr2 | 96698359 | |||||||
chr2:96698666 | G | C | 1 | a0001c0020t0001g0025 | 1 | NA18986.hp1 | splice_region_variant&intron_variant | LOW | c.4357-5G>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 40/52 | chr2 | 96698666 | |||||||
chr2:96699027 | A | C | 3 | a0002c0001t0001g0026 a0002c0001t0001g0028 a0002c0001t0001g0050 |
3 | HG02132.hp1 HG02155.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.4519-18A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 41/52 | chr2 | 96699027 | |||||||
chr2:96699036 | T | C | 3 | a0002c0001t0001g0026 a0002c0001t0001g0028 a0002c0001t0001g0050 |
3 | HG02132.hp1 HG02155.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.4519-9T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 41/52 | chr2 | 96699036 | |||||||
chr2:96699296 | T | C | 1 | a0005c0007t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4610+160T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 42/52 | chr2 | 96699296 | |||||||
chr2:96699308 | G | A | 1 | a0002c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4610+172G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 42/52 | chr2 | 96699308 | |||||||
chr2:96699321 | T | C | 1 | a0001c0002t0001g0189 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4610+185T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 42/52 | chr2 | 96699321 | |||||||
chr2:96699476 | C | T | 13 | a0001c0003t0001g0178 a0001c0003t0001g0181 a0001c0003t0001g0186 others(10): Show |
13 | HG01081.hp1 HG02040.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.4611-74C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 42/52 | chr2 | 96699476 | |||||||
chr2:96700249 | C | T | 1 | a0002c0001t0001g0003 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4931-83C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 44/52 | chr2 | 96700249 | |||||||
chr2:96700523 | G | A | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5070+52G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96700523 | |||||||
chr2:96700566 | A | G | 170 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0017 others(167): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.5070+95A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96700566 | |||||||
chr2:96700587 | A | G | 52 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(49): Show |
52 | HG00597.hp2 HG00642.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.5070+116A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96700587 | |||||||
chr2:96700809 | C | T | 1 | a0002c0001t0001g0121 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5070+338C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96700809 | |||||||
chr2:96700862 | A | G | 26 | a0001c0003t0001g0196 a0001c0004t0001g0002 a0001c0004t0001g0007 others(23): Show |
26 | HG00597.hp2 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.5070+391A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96700862 | |||||||
chr2:96701042 | A | G | 57 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0011 others(54): Show |
57 | HG00597.hp2 HG00642.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.5070+571A>G | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96701042 | |||||||
chr2:96701084 | G | A | 4 | a0001c0003t0001g0062 a0001c0003t0001g0078 a0001c0003t0001g0079 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.5070+613G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96701084 | |||||||
chr2:96701389 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5071-566G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96701389 | |||||||
chr2:96701615 | A | C | 1 | a0002c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5071-340A>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96701615 | |||||||
chr2:96701830 | C | T | 1 | a0002c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5071-125C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 45/52 | chr2 | 96701830 | |||||||
chr2:96702072 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5159+29G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 46/52 | chr2 | 96702072 | |||||||
chr2:96702512 | C | T | 1 | a0001c0003t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5256-88C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 47/52 | chr2 | 96702512 | |||||||
chr2:96702515 | C | T | 1 | a0001c0003t0001g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5256-85C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 47/52 | chr2 | 96702515 | |||||||
chr2:96702933 | G | A | 3 | a0002c0001t0001g0052 a0002c0001t0001g0064 a0009c0025t0001g0153 |
3 | HG00099.hp1 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.5398-45G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 48/52 | chr2 | 96702933 | |||||||
chr2:96702949 | G | A | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5398-29G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 48/52 | chr2 | 96702949 | |||||||
chr2:96703809 | C | CT | 18 | a0001c0002t0001g0039 a0001c0003t0001g0141 a0001c0003t0001g0200 others(15): Show |
18 | HG00099.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.5801+200dupT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | INFO_REALIGN_3_PRIME | chr2 | 96703809 | ||||||
chr2:96703809 | CT | C | 91 | a0001c0002t0001g0014 a0001c0002t0001g0027 a0001c0002t0001g0056 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.5801+200delT | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | INFO_REALIGN_3_PRIME | chr2 | 96703809 | ||||||
chr2:96703809 | CTT | C | 10 | a0001c0002t0001g0101 a0001c0002t0001g0106 a0001c0004t0001g0007 others(7): Show |
10 | HG01358.hp1 HG01975.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.5801+199_5801+200d others(4): Show |
FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | INFO_REALIGN_3_PRIME | chr2 | 96703809 | ||||||
chr2:96703810 | T | C | 3 | a0001c0003t0001g0062 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5801+178T>C | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | chr2 | 96703810 | |||||||
chr2:96703872 | G | A | 1 | a0011c0018t0001g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5801+240G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | chr2 | 96703872 | |||||||
chr2:96703936 | C | T | 1 | a0002c0001t0001g0142 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5802-279C>T | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | chr2 | 96703936 | |||||||
chr2:96704005 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5802-210G>A | FER1L5 | ENSG00000249715.13 | transcript | ENST00000624922.6 | protein_coding | 51/52 | chr2 | 96704005 |