Item | Value |
---|---|
geneid | 440275 |
ensemblid | ENSG00000128829.12 |
hgncid | 19687 |
symbol | EIF2AK4 |
name | eukaryotic translation initiation factor 2 alpha kinase 4 |
refseq_nuc | NM_001013703.4 |
refseq_prot | NP_001013725.2 |
ensembl_nuc | ENST00000263791.10 |
ensembl_prot | ENSP00000263791.5 |
mane_status | MANE Select |
chr | chr15 |
start | 39934115 |
end | 40035591 |
strand | + |
ver | v1.2 |
region | chr15:39934115-40035591 |
region5000 | chr15:39929115-40040591 |
regionname0 | EIF2AK4_chr15_39934115_40035591 |
regionname5000 | EIF2AK4_chr15_39929115_40040591 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1649 | 126 | 18 | 10 | 90 | 3 | 5 | 65 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0002 | 0/1 | 1649 | 120 | 50 | 22 | 29 | 6 | 12 | 24 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0003 | 1/0 | 1649 | 61 | 7 | 11 | 41 | 0 | 1 | 30 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0004 | 0/0 | 1651 | 27 | 3 | 5 | 12 | 0 | 7 | 10 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1646): Show |
chr15 | 39929115 | 40040591 |
a0005 | 0/0 | 1649 | 10 | 1 | 4 | 1 | 1 | 3 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0006 | 0/0 | 732 | 5 | 1 | 0 | 2 | 0 | 2 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(727): Show |
chr15 | 39929115 | 40040591 |
a0007 | 0/0 | 1649 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0008 | 0/0 | 1649 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0009 | 0/0 | 1649 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0010 | 0/0 | 1649 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0011 | 0/0 | 732 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(727): Show |
chr15 | 39929115 | 40040591 |
a0012 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0013 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0014 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0015 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(727): Show |
chr15 | 39929115 | 40040591 |
a0016 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
a0017 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | MAGGR others(1644): Show |
chr15 | 39929115 | 40040591 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4947 | 104 | 11 | 7 | 81 | 1 | 4 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0001c0005 | 0/0 | 4947 | 18 | 7 | 3 | 6 | 2 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0001c0020 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0001c0021 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0001c0022 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0001c0033 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0002 | 0/0 | 4947 | 56 | 35 | 8 | 4 | 4 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0004 | 0/0 | 4947 | 51 | 11 | 11 | 21 | 1 | 7 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0011 | 0/0 | 4947 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0013 | 0/1 | 4947 | 4 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0019 | 0/0 | 4947 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0029 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0030 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0002c0031 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0003c0003 | 0/0 | 4947 | 54 | 3 | 11 | 39 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0003c0010 | 0/0 | 4947 | 4 | 2 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0003c0025 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0003c0026 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0003c0036 | 1/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0004c0006 | 0/0 | 4953 | 14 | 3 | 3 | 3 | 0 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4948): Show |
chr15 | 39929115 | 40040591 | ||
a0004c0007 | 0/0 | 4953 | 12 | 0 | 1 | 9 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4948): Show |
chr15 | 39929115 | 40040591 | ||
a0004c0037 | 0/0 | 4953 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4948): Show |
chr15 | 39929115 | 40040591 | ||
a0005c0008 | 0/0 | 4947 | 6 | 1 | 1 | 1 | 1 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0005c0014 | 0/0 | 4947 | 4 | 0 | 3 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0006c0012 | 0/0 | 4948 | 4 | 0 | 0 | 2 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4943): Show |
chr15 | 39929115 | 40040591 | ||
a0006c0032 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4943): Show |
chr15 | 39929115 | 40040591 | ||
a0007c0009 | 0/0 | 4947 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0008c0015 | 0/0 | 4947 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0009c0016 | 0/0 | 4947 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0010c0018 | 0/0 | 4947 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0011c0017 | 0/0 | 4948 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4943): Show |
chr15 | 39929115 | 40040591 | ||
a0012c0028 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0013c0027 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0014c0035 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0015c0023 | 0/0 | 4948 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4943): Show |
chr15 | 39929115 | 40040591 | ||
a0016c0034 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 | ||
a0017c0024 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | ATGGC others(4942): Show |
chr15 | 39929115 | 40040591 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5538 | 21 | 1 | 3 | 16 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0002 | 0/0 | 5538 | 29 | 1 | 1 | 25 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0003 | 0/0 | 5538 | 43 | 1 | 3 | 37 | 1 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0004 | 0/0 | 5538 | 2 | 1 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0005 | 0/0 | 5537 | 7 | 7 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0011 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0001c0001t0012 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0001c0005t0001 | 0/0 | 5538 | 11 | 4 | 1 | 4 | 2 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0005t0002 | 0/0 | 5538 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0005t0004 | 0/0 | 5538 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0005t0005 | 0/0 | 5537 | 4 | 3 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0001c0020t0001 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0021t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0022t0002 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0001c0033t0001 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0001 | 0/0 | 5538 | 23 | 7 | 7 | 0 | 4 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0002 | 0/0 | 5538 | 14 | 13 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0003 | 0/0 | 5538 | 8 | 5 | 1 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0004 | 0/0 | 5538 | 6 | 6 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0005 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0007 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0008 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0002t0010 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0001 | 0/0 | 5538 | 31 | 1 | 11 | 13 | 0 | 6 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0002 | 0/0 | 5538 | 9 | 4 | 0 | 5 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0003 | 0/0 | 5538 | 5 | 3 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0004 | 0/0 | 5538 | 2 | 0 | 0 | 0 | 1 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0005 | 0/0 | 5537 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0002c0004t0014 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0011t0002 | 0/0 | 5538 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0013t0001 | 0/1 | 5538 | 4 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0019t0001 | 0/0 | 5538 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0029t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0030t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0002c0031t0009 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0001 | 0/0 | 5538 | 6 | 2 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0002 | 0/0 | 5538 | 42 | 1 | 10 | 30 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0003 | 0/0 | 5538 | 3 | 0 | 1 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0004 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0006 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0003t0013 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0010t0001 | 0/0 | 5538 | 4 | 2 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0025t0004 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0026t0001 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0003c0036t0003 | 1/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0004c0006t0001 | 0/0 | 5544 | 5 | 0 | 2 | 2 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0006t0002 | 0/0 | 5544 | 2 | 0 | 0 | 1 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0006t0003 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0006t0004 | 0/0 | 5544 | 3 | 0 | 1 | 0 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0006t0006 | 0/0 | 5544 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0007t0001 | 0/0 | 5544 | 7 | 0 | 0 | 5 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0007t0002 | 0/0 | 5544 | 4 | 0 | 1 | 3 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0007t0003 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0004c0037t0001 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5539): Show |
chr15 | 39929115 | 40040591 |
a0005c0008t0001 | 0/0 | 5538 | 3 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0005c0008t0004 | 0/0 | 5538 | 3 | 0 | 0 | 1 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0005c0014t0004 | 0/0 | 5538 | 4 | 0 | 3 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0006c0012t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0006c0012t0002 | 0/0 | 5539 | 2 | 0 | 0 | 1 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0006c0012t0003 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0006c0032t0005 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0007c0009t0003 | 0/0 | 5538 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0008c0015t0005 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0008c0015t0006 | 0/0 | 5538 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0009c0016t0007 | 0/0 | 5538 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0010c0018t0005 | 0/0 | 5537 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5532): Show |
chr15 | 39929115 | 40040591 |
a0011c0017t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0011c0017t0003 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0012c0028t0002 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0013c0027t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0014c0035t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0015c0023t0003 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5534): Show |
chr15 | 39929115 | 40040591 |
a0016c0034t0001 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
a0017c0024t0002 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | AGCGC others(5533): Show |
chr15 | 39929115 | 40040591 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0005t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0020t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0021t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0022t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0001c0033t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0002t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0004t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0011t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0011t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0011t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0011t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0013t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0013t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0013t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0013t0001g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0019t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0019t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0029t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0030t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0002c0031t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0003t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0010t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0025t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0026t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0003c0036t0003g0354 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0006t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0007t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0004c0037t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0008t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0008t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0008t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0008t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0014t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0014t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0005c0014t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0006c0012t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0006c0012t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0006c0012t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0006c0012t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0006c0032t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0007c0009t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0007c0009t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0007c0009t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0007c0009t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0008c0015t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0008c0015t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0008c0015t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0009c0016t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0009c0016t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0010c0018t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0010c0018t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0011c0017t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0011c0017t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0012c0028t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0013c0027t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0014c0035t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0015c0023t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0016c0034t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
a0017c0024t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0289 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00099 | hp2 | a0001 | c0005 | t0001 | g0225 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0175 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0270 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00280 | hp1 | a0001 | c0005 | t0001 | g0135 | EUR | FIN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0297 | EUR | FIN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00408 | hp1 | a0003 | c0003 | t0004 | g0074 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00544 | hp1 | a0002 | c0004 | t0001 | g0257 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00544 | hp2 | a0004 | c0007 | t0002 | g0214 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00609 | hp1 | a0004 | c0006 | t0001 | g0210 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0152 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00621 | hp2 | a0003 | c0010 | t0001 | g0079 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00639 | hp2 | a0002 | c0013 | t0001 | g0280 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00642 | hp1 | a0002 | c0004 | t0001 | g0358 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0276 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00673 | hp1 | a0003 | c0003 | t0006 | g0105 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00741 | hp1 | a0001 | c0005 | t0005 | g0153 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG00741 | hp2 | a0002 | c0004 | t0001 | g0326 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0005 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01074 | hp1 | a0002 | c0004 | t0001 | g0274 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01074 | hp2 | a0004 | c0006 | t0004 | g0248 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0360 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01099 | hp1 | a0002 | c0019 | t0001 | g0281 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01099 | hp2 | a0003 | c0003 | t0002 | g0066 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01106 | hp1 | a0002 | c0004 | t0001 | g0325 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01106 | hp2 | a0004 | c0037 | t0001 | g0273 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0060 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01168 | hp1 | a0004 | c0006 | t0001 | g0259 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01169 | hp1 | a0005 | c0008 | t0001 | g0356 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01175 | hp1 | a0002 | c0004 | t0001 | g0324 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01175 | hp2 | a0002 | c0019 | t0001 | g0284 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01255 | hp1 | a0009 | c0016 | t0007 | g0042 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01256 | hp2 | a0002 | c0004 | t0001 | g0322 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0209 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01257 | hp2 | a0005 | c0014 | t0004 | g0006 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01258 | hp1 | a0005 | c0014 | t0004 | g0006 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01346 | hp1 | a0002 | c0004 | t0001 | g0329 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01346 | hp2 | a0003 | c0003 | t0002 | g0102 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0290 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01361 | hp2 | a0002 | c0004 | t0001 | g0328 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01496 | hp1 | a0003 | c0003 | t0002 | g0063 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01496 | hp2 | a0010 | c0018 | t0005 | g0240 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01516 | hp1 | a0002 | c0013 | t0001 | g0278 | EUR | IBS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01516 | hp2 | a0005 | c0008 | t0001 | g0296 | EUR | IBS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01884 | hp1 | a0002 | c0031 | t0009 | g0045 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01884 | hp2 | a0002 | c0004 | t0002 | g0272 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0018 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01891 | hp2 | a0002 | c0004 | t0003 | g0036 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01975 | hp2 | a0003 | c0003 | t0002 | g0064 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0065 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01978 | hp2 | a0004 | c0007 | t0002 | g0262 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01981 | hp1 | a0004 | c0006 | t0001 | g0261 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01981 | hp2 | a0003 | c0003 | t0002 | g0101 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02004 | hp2 | a0003 | c0003 | t0002 | g0061 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02015 | hp2 | a0003 | c0003 | t0002 | g0230 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02027 | hp2 | a0003 | c0003 | t0002 | g0104 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02040 | hp2 | a0001 | c0021 | t0003 | g0223 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02055 | hp2 | a0002 | c0030 | t0002 | g0305 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02056 | hp1 | a0001 | c0022 | t0002 | g0168 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02071 | hp1 | a0003 | c0003 | t0002 | g0089 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02074 | hp2 | a0005 | c0008 | t0004 | g0339 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02080 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02135 | hp1 | a0002 | c0004 | t0003 | g0263 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02145 | hp1 | a0011 | c0017 | t0002 | g0239 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02148 | hp1 | a0001 | c0005 | t0001 | g0134 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02148 | hp2 | a0003 | c0003 | t0002 | g0062 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02155 | hp1 | a0002 | c0004 | t0001 | g0315 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0246 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02258 | hp2 | a0002 | c0029 | t0002 | g0306 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0098 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0125 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02300 | hp1 | a0005 | c0014 | t0004 | g0291 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02300 | hp2 | a0002 | c0004 | t0001 | g0321 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02451 | hp1 | a0001 | c0005 | t0005 | g0123 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02451 | hp2 | a0003 | c0010 | t0001 | g0047 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02523 | hp2 | a0003 | c0003 | t0003 | g0091 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02572 | hp1 | a0002 | c0002 | t0005 | g0292 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02572 | hp2 | a0002 | c0002 | t0010 | g0046 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02615 | hp1 | a0004 | c0006 | t0006 | g0252 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02615 | hp2 | a0002 | c0004 | t0005 | g0237 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0343 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02630 | hp2 | a0002 | c0004 | t0003 | g0038 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02698 | hp1 | a0004 | c0006 | t0001 | g0255 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02717 | hp1 | a0004 | c0006 | t0006 | g0251 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0304 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02723 | hp2 | a0002 | c0004 | t0001 | g0041 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02738 | hp1 | a0012 | c0028 | t0002 | g0307 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02738 | hp2 | a0006 | c0012 | t0003 | g0269 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02809 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0359 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02886 | hp1 | a0002 | c0004 | t0002 | g0353 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02886 | hp2 | a0003 | c0026 | t0001 | g0011 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0337 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02896 | hp2 | a0002 | c0004 | t0005 | g0037 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0336 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02922 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0338 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0334 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02976 | hp1 | a0008 | c0015 | t0006 | g0025 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02976 | hp2 | a0002 | c0002 | t0004 | g0236 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03041 | hp2 | a0008 | c0015 | t0006 | g0027 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03098 | hp1 | a0011 | c0017 | t0003 | g0341 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03098 | hp2 | a0013 | c0027 | t0002 | g0024 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0034 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03139 | hp1 | a0010 | c0018 | t0005 | g0238 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0308 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03195 | hp1 | a0002 | c0002 | t0003 | g0050 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03209 | hp1 | a0002 | c0004 | t0002 | g0314 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03209 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03225 | hp1 | a0004 | c0006 | t0006 | g0260 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0335 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03239 | hp1 | a0002 | c0004 | t0004 | g0330 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03239 | hp2 | a0004 | c0007 | t0001 | g0264 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0351 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03490 | hp1 | a0004 | c0006 | t0003 | g0344 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03490 | hp2 | a0005 | c0008 | t0004 | g0004 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03492 | hp1 | a0005 | c0008 | t0004 | g0004 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03492 | hp2 | a0002 | c0004 | t0001 | g0347 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03516 | hp1 | a0001 | c0005 | t0005 | g0108 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03540 | hp1 | a0002 | c0004 | t0002 | g0275 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03540 | hp2 | a0002 | c0004 | t0005 | g0114 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0350 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0016 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03654 | hp2 | a0004 | c0006 | t0004 | g0249 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03669 | hp1 | a0001 | c0033 | t0001 | g0131 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03669 | hp2 | a0006 | c0012 | t0002 | g0176 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03710 | hp1 | a0004 | c0007 | t0001 | g0250 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03710 | hp2 | a0002 | c0004 | t0001 | g0327 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03942 | hp1 | a0002 | c0004 | t0001 | g0277 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03942 | hp2 | a0005 | c0014 | t0004 | g0294 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04115 | hp1 | a0002 | c0004 | t0001 | g0357 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04115 | hp2 | a0004 | c0006 | t0004 | g0265 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04184 | hp1 | a0002 | c0004 | t0001 | g0051 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04184 | hp2 | a0004 | c0006 | t0002 | g0253 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18522 | hp1 | a0003 | c0025 | t0004 | g0010 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0241 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18612 | hp1 | a0003 | c0003 | t0002 | g0100 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18747 | hp1 | a0001 | c0005 | t0001 | g0137 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18747 | hp2 | a0001 | c0005 | t0002 | g0195 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18906 | hp1 | a0003 | c0010 | t0001 | g0048 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18906 | hp2 | a0008 | c0015 | t0005 | g0026 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18940 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18940 | hp2 | a0002 | c0004 | t0002 | g0311 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18941 | hp1 | a0002 | c0004 | t0003 | g0256 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18944 | hp1 | a0002 | c0004 | t0002 | g0316 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18946 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18947 | hp2 | a0002 | c0004 | t0001 | g0320 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0163 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0318 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18949 | hp2 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18950 | hp1 | a0001 | c0005 | t0002 | g0220 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18950 | hp2 | a0002 | c0002 | t0008 | g0323 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18951 | hp2 | a0002 | c0004 | t0014 | g0302 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18952 | hp1 | a0002 | c0004 | t0002 | g0228 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18953 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18953 | hp2 | a0002 | c0011 | t0002 | g0331 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18956 | hp1 | a0003 | c0003 | t0002 | g0053 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18957 | hp2 | a0006 | c0012 | t0002 | g0150 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18962 | hp2 | a0003 | c0003 | t0002 | g0083 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18964 | hp1 | a0007 | c0009 | t0003 | g0231 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18965 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18969 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0300 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18972 | hp1 | a0004 | c0007 | t0003 | g0258 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18972 | hp2 | a0014 | c0035 | t0003 | g0235 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18974 | hp1 | a0007 | c0009 | t0003 | g0233 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18974 | hp2 | a0001 | c0005 | t0001 | g0180 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18975 | hp1 | a0001 | c0020 | t0001 | g0173 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18977 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18979 | hp2 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0312 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18984 | hp2 | a0002 | c0004 | t0001 | g0352 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0155 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18990 | hp2 | a0002 | c0004 | t0001 | g0319 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18991 | hp2 | a0004 | c0007 | t0002 | g0266 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18992 | hp2 | a0004 | c0007 | t0001 | g0213 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18993 | hp1 | a0007 | c0009 | t0003 | g0229 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18993 | hp2 | a0004 | c0006 | t0002 | g0211 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18995 | hp1 | a0004 | c0007 | t0001 | g0212 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19001 | hp2 | a0002 | c0004 | t0001 | g0349 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19002 | hp1 | a0002 | c0004 | t0001 | g0342 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19004 | hp2 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19006 | hp1 | a0002 | c0011 | t0002 | g0346 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19006 | hp2 | a0006 | c0012 | t0001 | g0267 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19010 | hp2 | a0002 | c0004 | t0002 | g0348 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0317 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19012 | hp1 | a0002 | c0004 | t0002 | g0332 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19030 | hp1 | a0003 | c0003 | t0002 | g0059 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19043 | hp1 | a0005 | c0008 | t0001 | g0298 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0310 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19054 | hp2 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19056 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19060 | hp1 | a0003 | c0010 | t0001 | g0077 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19060 | hp2 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19064 | hp1 | a0004 | c0007 | t0001 | g0215 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19064 | hp2 | a0004 | c0006 | t0001 | g0254 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0271 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19067 | hp2 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19068 | hp1 | a0002 | c0004 | t0001 | g0303 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19068 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19070 | hp1 | a0004 | c0007 | t0002 | g0247 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19072 | hp2 | a0003 | c0003 | t0013 | g0086 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19075 | hp2 | a0004 | c0007 | t0001 | g0216 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19077 | hp1 | a0002 | c0011 | t0002 | g0096 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19079 | hp1 | a0003 | c0003 | t0002 | g0052 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19079 | hp2 | a0007 | c0009 | t0003 | g0234 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19080 | hp1 | a0002 | c0011 | t0002 | g0301 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19081 | hp2 | a0004 | c0007 | t0001 | g0227 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0097 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19084 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0132 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19086 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19087 | hp1 | a0003 | c0003 | t0002 | g0103 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19087 | hp2 | a0015 | c0023 | t0003 | g0232 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19088 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19090 | hp1 | a0002 | c0004 | t0001 | g0345 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19091 | hp1 | a0016 | c0034 | t0001 | g0149 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0019 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA19240 | hp2 | a0009 | c0016 | t0007 | g0044 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20752 | hp1 | a0002 | c0004 | t0004 | g0340 | EUR | TSI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0286 | EUR | TSI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20905 | hp1 | a0002 | c0004 | t0001 | g0005 | SAS | GIH | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20905 | hp2 | a0017 | c0024 | t0002 | g0068 | SAS | GIH | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01123 | hp1 | a0003 | c0003 | t0002 | g0107 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG01123 | hp2 | a0001 | c0005 | t0004 | g0121 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02486 | hp1 | a0002 | c0013 | t0001 | g0279 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02486 | hp2 | a0002 | c0002 | t0007 | g0043 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02559 | hp1 | a0001 | c0005 | t0005 | g0124 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0313 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03471 | hp1 | a0006 | c0032 | t0005 | g0122 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0049 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0161 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0309 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
NA20300 | hp2 | a0002 | c0004 | t0003 | g0039 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
homoSapiens | chm13v2 | a0002 | c0013 | t0001 | g0282 | REF | REF | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
homoSapiens | grch38p0 | a0003 | c0036 | t0003 | g0354 | REF | REF | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:39967647 | A | C | 5 | a0001 a0006 a0008 others(2): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
missense_variant | MODERATE | c.1321A>C | p.Ile441Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/39 | 1402/5538 | 1321/4950 | 441/1649 | chr15 | 39967647 | |||
chr15:39967801 | G | A | 1 | a0009 | 2 | HG01255.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1475G>A | p.Ser492Asn | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/39 | 1556/5538 | 1475/4950 | 492/1649 | chr15 | 39967801 | |||
chr15:39973598 | A | G | 13 | a0001 a0002 a0004 others(10): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.1667A>G | p.Glu556Gly | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/39 | 1748/5538 | 1667/4950 | 556/1649 | chr15 | 39973598 | |||
chr15:39973625 | T | C | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1694T>C | p.Ile565Thr | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/39 | 1775/5538 | 1694/4950 | 565/1649 | chr15 | 39973625 | |||
chr15:39976615 | C | T | 1 | a0008 | 3 | HG02976.hp1 HG03041.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2020C>T | p.Pro674Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2101/5538 | 2020/4950 | 674/1649 | chr15 | 39976615 | |||
chr15:39976763 | T | TC | 3 | a0006 a0011 a0015 |
8 | HG02145.hp1 HG02738.hp2 HG03098.hp1 others(5): Show |
frameshift_variant | HIGH | c.2172dupC | p.Ala725fs | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2254/5538 | 2173/4950 | 725/1649 | INFO_REALIGN_3_PRIME | chr15 | 39976763 | ||
chr15:39976797 | G | GGACGAC | 1 | a0004 | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
disruptive_inframe_insertion | MODERATE | c.2208_2213dupCGACGA | p.Asp736_Asp737dup | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2295/5538 | 2214/4950 | 738/1649 | INFO_REALIGN_3_PRIME | chr15 | 39976797 | ||
chr15:39992205 | G | C | 2 | a0007 a0015 |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
missense_variant | MODERATE | c.2662G>C | p.Asp888His | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/39 | 2743/5538 | 2662/4950 | 888/1649 | chr15 | 39992205 | |||
chr15:40002770 | C | T | 1 | a0017 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3217C>T | p.Arg1073Cys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 22/39 | 3298/5538 | 3217/4950 | 1073/1649 | chr15 | 40002770 | |||
chr15:40008148 | A | G | 1 | a0014 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.3529A>G | p.Ile1177Val | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/39 | 3610/5538 | 3529/4950 | 1177/1649 | chr15 | 40008148 | |||
chr15:40016509 | G | A | 1 | a0012 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.3767G>A | p.Arg1256Gln | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/39 | 3848/5538 | 3767/4950 | 1256/1649 | chr15 | 40016509 | |||
chr15:40016658 | G | T | 1 | a0005 | 10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
missense_variant | MODERATE | c.3916G>T | p.Gly1306Cys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/39 | 3997/5538 | 3916/4950 | 1306/1649 | chr15 | 40016658 | |||
chr15:40017184 | A | G | 1 | a0010 | 2 | HG01496.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.4007A>G | p.Lys1336Arg | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/39 | 4088/5538 | 4007/4950 | 1336/1649 | chr15 | 40017184 | |||
chr15:40020943 | G | T | 1 | a0016 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.4218G>T | p.Gln1406His | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/39 | 4299/5538 | 4218/4950 | 1406/1649 | chr15 | 40020943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:39934294 | T | C | 32 | a0001c0001 a0001c0005 a0001c0020 others(29): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
synonymous_variant | LOW | c.99T>C | p.Ile33Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 180/5538 | 99/4950 | 33/1649 | chr15 | 39934294 | |||
chr15:39939570 | T | C | 1 | a0001c0020 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.210T>C | p.Tyr70Tyr | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/39 | 291/5538 | 210/4950 | 70/1649 | chr15 | 39939570 | |||
chr15:39943399 | T | C | 1 | a0001c0021 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.274T>C | p.Leu92Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/39 | 355/5538 | 274/4950 | 92/1649 | chr15 | 39943399 | |||
chr15:39955634 | T | C | 1 | a0001c0022 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.609T>C | p.Ile203Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/39 | 690/5538 | 609/4950 | 203/1649 | chr15 | 39955634 | |||
chr15:39976563 | C | T | 1 | a0002c0031 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1968C>T | p.Ile656Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2049/5538 | 1968/4950 | 656/1649 | chr15 | 39976563 | |||
chr15:39985879 | A | G | 2 | a0003c0025 a0003c0026 |
2 | HG02886.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.2394A>G | p.Leu798Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/39 | 2475/5538 | 2394/4950 | 798/1649 | chr15 | 39985879 | |||
chr15:40001212 | C | T | 1 | a0002c0030 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.3147C>T | p.Ser1049Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/39 | 3228/5538 | 3147/4950 | 1049/1649 | chr15 | 40001212 | |||
chr15:40020940 | C | T | 12 | a0001c0005 a0001c0020 a0002c0004 others(9): Show |
99 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(96): Show |
synonymous_variant | LOW | c.4215C>T | p.Gly1405Gly | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/39 | 4296/5538 | 4215/4950 | 1405/1649 | chr15 | 40020940 | |||
chr15:40026055 | C | T | 1 | a0002c0011 | 4 | NA18953.hp2 NA19006.hp1 NA19077.hp1 others(1): Show |
synonymous_variant | LOW | c.4468C>T | p.Leu1490Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/39 | 4549/5538 | 4468/4950 | 1490/1649 | chr15 | 40026055 | |||
chr15:40029415 | C | T | 1 | a0001c0033 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.4512C>T | p.Ser1504Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/39 | 4593/5538 | 4512/4950 | 1504/1649 | chr15 | 40029415 | |||
chr15:40034403 | A | G | 1 | a0002c0029 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.4851A>G | p.Lys1617Lys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/39 | 4932/5538 | 4851/4950 | 1617/1649 | chr15 | 40034403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:39934176 | G | A | 1 | a0002c0002t0008 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 20 | chr15 | 39934176 | ||||||
chr15:39934184 | C | A | 4 | a0002c0002t0007 a0002c0002t0010 a0002c0031t0009 others(1): Show |
5 | HG01255.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-12C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 12 | chr15 | 39934184 | ||||||
chr15:40035089 | A | G | 21 | a0001c0001t0002 a0001c0001t0012 a0001c0005t0002 others(18): Show |
120 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 5 | chr15 | 40035089 | ||||||
chr15:40035100 | G | A | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(25): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 16 | chr15 | 40035100 | ||||||
chr15:40035179 | C | T | 3 | a0003c0003t0006 a0004c0006t0006 a0008c0015t0006 |
6 | HG00673.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*95C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 95 | chr15 | 40035179 | ||||||
chr15:40035479 | GA | G | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(6): Show |
22 | HG00741.hp1 HG01496.hp2 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*405delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 405 | INFO_REALIGN_3_PRIME | chr15 | 40035479 | |||||
chr15:40035488 | A | T | 1 | a0003c0003t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 404 | chr15 | 40035488 | ||||||
chr15:40035489 | A | T | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(41): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 405 | chr15 | 40035489 | ||||||
chr15:40035497 | C | G | 9 | a0001c0001t0004 a0001c0005t0004 a0002c0002t0004 others(6): Show |
23 | HG00408.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 413 | chr15 | 40035497 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:39934359 | G | C | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.144+20G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934359 | |||||||
chr15:39934502 | G | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.144+163G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934502 | |||||||
chr15:39934676 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(261): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.144+337T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934676 | |||||||
chr15:39934791 | G | A | 1 | a0001c0001t0002g0009 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.144+452G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934791 | |||||||
chr15:39934814 | A | G | 1 | a0002c0002t0001g0361 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.144+475A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934814 | |||||||
chr15:39934881 | G | A | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.144+542G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934881 | |||||||
chr15:39934888 | C | G | 1 | a0002c0002t0001g0360 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.144+549C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934888 | |||||||
chr15:39934956 | C | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.144+617C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934956 | |||||||
chr15:39934971 | G | A | 1 | a0001c0001t0003g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.144+632G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934971 | |||||||
chr15:39935072 | A | G | 1 | a0001c0001t0003g0268 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.144+733A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935072 | |||||||
chr15:39935337 | C | CT | 21 | a0002c0004t0001g0257 a0002c0004t0003g0256 a0002c0004t0003g0263 others(18): Show |
21 | HG00544.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.144+1011dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr15 | 39935337 | ||||||
chr15:39935412 | C | G | 2 | a0001c0001t0003g0245 a0001c0005t0001g0246 |
2 | HG01081.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.144+1073C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935412 | |||||||
chr15:39935557 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0004g0244 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.144+1218C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935557 | |||||||
chr15:39935624 | C | T | 1 | a0002c0002t0001g0359 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144+1285C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935624 | |||||||
chr15:39935977 | G | A | 1 | a0001c0001t0002g0009 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.144+1638G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935977 | |||||||
chr15:39936018 | G | T | 7 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(4): Show |
7 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+1679G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936018 | |||||||
chr15:39936376 | A | G | 8 | a0002c0004t0002g0228 a0003c0003t0002g0230 a0007c0009t0003g0229 others(5): Show |
8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+2037A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936376 | |||||||
chr15:39936409 | C | T | 1 | a0004c0007t0001g0227 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.144+2070C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936409 | |||||||
chr15:39936455 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(128): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.144+2116C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936455 | |||||||
chr15:39936699 | G | A | 3 | a0001c0001t0003g0245 a0001c0005t0001g0246 a0001c0005t0005g0108 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.144+2360G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936699 | |||||||
chr15:39936996 | T | C | 6 | a0001c0001t0001g0112 a0001c0001t0002g0111 a0001c0001t0003g0109 others(3): Show |
6 | HG00621.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-2509T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936996 | |||||||
chr15:39937039 | A | G | 2 | a0002c0004t0001g0357 a0002c0004t0001g0358 |
2 | HG00642.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.145-2466A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937039 | |||||||
chr15:39937046 | A | C | 86 | a0001c0001t0002g0090 a0002c0002t0002g0241 a0002c0002t0002g0242 others(83): Show |
86 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.145-2459A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937046 | |||||||
chr15:39937200 | A | G | 1 | a0005c0008t0001g0356 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.145-2305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937200 | |||||||
chr15:39937281 | G | A | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-2224G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937281 | |||||||
chr15:39937502 | A | G | 8 | a0002c0004t0002g0228 a0003c0003t0002g0230 a0007c0009t0003g0229 others(5): Show |
8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-2003A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937502 | |||||||
chr15:39937622 | C | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(129): Show |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.145-1883C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937622 | |||||||
chr15:39937650 | C | T | 71 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1855C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937650 | |||||||
chr15:39937720 | T | G | 35 | a0001c0001t0005g0014 a0001c0001t0005g0023 a0001c0001t0005g0028 others(32): Show |
35 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.145-1785T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937720 | |||||||
chr15:39937742 | T | G | 1 | a0001c0001t0005g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-1763T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937742 | |||||||
chr15:39937808 | A | C | 1 | a0001c0022t0002g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.145-1697A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937808 | |||||||
chr15:39938033 | C | G | 8 | a0002c0004t0002g0228 a0003c0003t0002g0230 a0007c0009t0003g0229 others(5): Show |
8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-1472C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938033 | |||||||
chr15:39938071 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.145-1434T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938071 | |||||||
chr15:39938200 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0226 a0001c0005t0001g0225 |
4 | HG00099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-1305C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938200 | |||||||
chr15:39938571 | C | A | 2 | a0003c0003t0002g0052 a0003c0003t0002g0053 |
2 | NA18956.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.145-934C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938571 | |||||||
chr15:39938609 | A | C | 6 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0004t0003g0036 others(3): Show |
6 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-896A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938609 | |||||||
chr15:39938817 | T | A | 2 | a0002c0002t0003g0049 a0002c0002t0003g0050 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.145-688T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938817 | |||||||
chr15:39938968 | A | G | 1 | a0003c0003t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.145-537A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938968 | |||||||
chr15:39939299 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.145-206A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939299 | |||||||
chr15:39939424 | A | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.145-81A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939424 | |||||||
chr15:39939473 | GAA | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | NA18941.hp2 NA18948.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-26_145-25delAA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr15 | 39939473 | ||||||
chr15:39939480 | A | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | NA18941.hp2 NA18948.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-25A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939480 | |||||||
chr15:39939800 | C | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.257+183C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39939800 | |||||||
chr15:39939914 | G | GA | 262 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(259): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.257+301dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39939914 | ||||||
chr15:39940159 | G | A | 28 | a0001c0001t0005g0014 a0001c0001t0005g0023 a0001c0001t0005g0028 others(25): Show |
28 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.257+542G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940159 | |||||||
chr15:39940221 | T | C | 1 | a0002c0002t0001g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.257+604T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940221 | |||||||
chr15:39940281 | A | G | 2 | a0003c0003t0001g0106 a0003c0003t0006g0105 |
2 | HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.257+664A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940281 | |||||||
chr15:39940409 | A | T | 11 | a0001c0001t0005g0014 a0001c0001t0005g0028 a0001c0001t0005g0029 others(8): Show |
11 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.257+792A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940409 | |||||||
chr15:39940665 | T | C | 1 | a0002c0004t0002g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.257+1048T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940665 | |||||||
chr15:39940671 | G | C | 357 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(354): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.257+1054G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940671 | |||||||
chr15:39940814 | C | T | 1 | a0001c0005t0001g0246 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.257+1197C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940814 | |||||||
chr15:39940851 | C | T | 27 | a0001c0001t0005g0014 a0001c0001t0005g0023 a0001c0001t0005g0028 others(24): Show |
27 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.257+1234C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940851 | |||||||
chr15:39941068 | A | G | 8 | a0002c0004t0002g0228 a0003c0003t0002g0230 a0007c0009t0003g0229 others(5): Show |
8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+1451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941068 | |||||||
chr15:39941108 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.257+1491T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941108 | |||||||
chr15:39941141 | C | T | 1 | a0002c0004t0002g0353 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.257+1524C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941141 | |||||||
chr15:39941179 | T | C | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+1562T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941179 | |||||||
chr15:39941279 | G | A | 73 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.257+1662G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941279 | |||||||
chr15:39941414 | C | T | 2 | a0001c0001t0003g0224 a0001c0021t0003g0223 |
2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+1797C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941414 | |||||||
chr15:39941441 | G | C | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA19057.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.257+1824G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941441 | |||||||
chr15:39941489 | A | AT | 8 | a0001c0001t0005g0014 a0001c0001t0005g0028 a0001c0001t0005g0029 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+1879dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39941489 | ||||||
chr15:39941491 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.257+1874T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941491 | |||||||
chr15:39941548 | TAAAG | T | 21 | a0001c0001t0005g0014 a0001c0001t0005g0023 a0001c0001t0005g0028 others(18): Show |
21 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.258-1831_258-1828d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39941548 | ||||||
chr15:39941717 | T | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-1666T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941717 | |||||||
chr15:39941760 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(55): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.258-1623C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941760 | |||||||
chr15:39941916 | A | G | 73 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.258-1467A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941916 | |||||||
chr15:39942029 | A | G | 7 | a0003c0003t0001g0099 a0003c0003t0002g0098 a0003c0003t0002g0100 others(4): Show |
7 | HG01346.hp2 HG01981.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-1354A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942029 | |||||||
chr15:39942047 | T | C | 8 | a0002c0004t0002g0228 a0003c0003t0002g0230 a0007c0009t0003g0229 others(5): Show |
8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-1336T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942047 | |||||||
chr15:39942398 | TC | T | 6 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0004t0003g0036 others(3): Show |
6 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-984delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942398 | |||||||
chr15:39942545 | T | C | 7 | a0002c0002t0007g0043 a0002c0002t0010g0046 a0002c0031t0009g0045 others(4): Show |
7 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-838T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942545 | |||||||
chr15:39942612 | T | C | 189 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(186): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.258-771T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942612 | |||||||
chr15:39942614 | G | C | 73 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.258-769G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942614 | |||||||
chr15:39942653 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.258-730G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942653 | |||||||
chr15:39942671 | G | T | 1 | a0003c0003t0002g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.258-712G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942671 | |||||||
chr15:39942715 | G | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-668G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942715 | |||||||
chr15:39942801 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(69): Show |
74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-582G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942801 | |||||||
chr15:39942957 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258-426G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942957 | |||||||
chr15:39942994 | G | A | 1 | a0002c0004t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.258-389G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942994 | |||||||
chr15:39943000 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-383G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943000 | |||||||
chr15:39943029 | A | AT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(76): Show |
81 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.258-339dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943029 | ||||||
chr15:39943033 | T | C | 21 | a0001c0001t0001g0355 a0002c0004t0001g0257 a0002c0004t0003g0256 others(18): Show |
21 | HG00544.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.258-350T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943033 | |||||||
chr15:39943097 | G | A | 1 | a0003c0003t0006g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258-286G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943097 | |||||||
chr15:39943177 | C | T | 1 | a0002c0004t0001g0352 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.258-206C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943177 | |||||||
chr15:39943188 | C | G | 1 | a0001c0001t0003g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.258-195C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943188 | |||||||
chr15:39943351 | C | CT | 100 | a0001c0001t0001g0355 a0001c0001t0002g0090 a0001c0001t0005g0014 others(97): Show |
101 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.258-12dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | ||||||
chr15:39943351 | C | CTT | 15 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(12): Show |
15 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-13_258-12dupTT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | ||||||
chr15:39943351 | CT | C | 84 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.258-12delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | ||||||
chr15:39943785 | G | A | 73 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.360+300G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943785 | |||||||
chr15:39943793 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.360+308A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943793 | |||||||
chr15:39943933 | C | G | 1 | a0002c0004t0001g0342 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.360+448C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943933 | |||||||
chr15:39943971 | A | AAAG | 94 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(91): Show |
96 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.360+495_360+497dup others(3): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39943971 | ||||||
chr15:39943984 | T | G | 1 | a0002c0004t0001g0352 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.360+499T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943984 | |||||||
chr15:39944008 | C | T | 1 | a0003c0003t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.360+523C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944008 | |||||||
chr15:39944171 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(259): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.360+686G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944171 | |||||||
chr15:39944175 | C | G | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.360+690C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944175 | |||||||
chr15:39944364 | G | A | 63 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.360+879G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944364 | |||||||
chr15:39944426 | C | T | 1 | a0002c0002t0002g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.360+941C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944426 | |||||||
chr15:39944432 | C | CTTTTTT | 87 | a0001c0001t0001g0355 a0002c0002t0002g0241 a0002c0002t0002g0242 others(84): Show |
87 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.360+959_360+964dup others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | ||||||
chr15:39944432 | C | CTTTTTTT | 29 | a0001c0001t0002g0090 a0001c0001t0003g0170 a0001c0001t0005g0023 others(26): Show |
29 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.360+958_360+964dup others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | ||||||
chr15:39944432 | C | CTTTTTTT others(1): Show |
113 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(110): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.360+957_360+964dup others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | ||||||
chr15:39944432 | C | CTTTTTTT others(2): Show |
22 | a0001c0001t0001g0112 a0001c0001t0001g0154 a0001c0001t0002g0156 others(19): Show |
22 | HG00609.hp2 HG00741.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.360+956_360+964dup others(9): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | ||||||
chr15:39944432 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0009 a0007c0009t0003g0233 a0007c0009t0003g0234 others(1): Show |
4 | NA18972.hp2 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+955_360+964dup others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | ||||||
chr15:39944455 | G | A | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360+970G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944455 | |||||||
chr15:39944462 | T | C | 1 | a0002c0004t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+977T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944462 | |||||||
chr15:39944480 | A | G | 1 | a0002c0004t0004g0340 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+995A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944480 | |||||||
chr15:39944488 | A | G | 20 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.360+1003A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944488 | |||||||
chr15:39944493 | G | C | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.360+1008G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944493 | |||||||
chr15:39944577 | A | G | 1 | a0001c0001t0003g0224 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.360+1092A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944577 | |||||||
chr15:39944634 | C | T | 5 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0003c0003t0001g0343 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+1149C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944634 | |||||||
chr15:39944684 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.360+1199C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944684 | |||||||
chr15:39944958 | T | C | 1 | a0001c0005t0004g0121 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.360+1473T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944958 | |||||||
chr15:39945014 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(342): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.360+1529A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945014 | |||||||
chr15:39945017 | T | A | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1532T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945017 | |||||||
chr15:39945040 | C | G | 8 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+1555C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945040 | |||||||
chr15:39945121 | G | A | 58 | a0002c0011t0002g0096 a0003c0003t0001g0058 a0003c0003t0001g0067 others(55): Show |
58 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.360+1636G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945121 | |||||||
chr15:39945513 | A | G | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360+2028A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945513 | |||||||
chr15:39945600 | CCTAAGAT others(15): Show |
C | 1 | a0005c0008t0004g0339 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.360+2119_360+2140d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39945600 | ||||||
chr15:39945643 | T | C | 1 | a0002c0004t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+2158T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945643 | |||||||
chr15:39945789 | G | A | 7 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(4): Show |
7 | HG02015.hp2 NA18964.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+2304G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945789 | |||||||
chr15:39945815 | A | C | 8 | a0004c0006t0001g0210 a0004c0006t0002g0211 a0004c0007t0001g0212 others(5): Show |
8 | HG00544.hp2 HG00609.hp1 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+2330A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945815 | |||||||
chr15:39945826 | C | T | 58 | a0002c0011t0002g0096 a0003c0003t0001g0058 a0003c0003t0001g0067 others(55): Show |
58 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.360+2341C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945826 | |||||||
chr15:39945944 | C | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.360+2459C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945944 | |||||||
chr15:39946174 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.360+2689A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946174 | |||||||
chr15:39946218 | G | A | 2 | a0002c0002t0001g0270 a0002c0002t0001g0360 |
2 | HG00140.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.360+2733G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946218 | |||||||
chr15:39946480 | T | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-2636T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946480 | |||||||
chr15:39946661 | T | C | 10 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(7): Show |
10 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.361-2455T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946661 | |||||||
chr15:39946752 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.361-2364C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946752 | |||||||
chr15:39946833 | C | T | 1 | a0001c0001t0001g0001 | 3 | NA18962.hp1 NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.361-2283C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946833 | |||||||
chr15:39946834 | G | A | 1 | a0002c0004t0001g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361-2282G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946834 | |||||||
chr15:39946891 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0004g0244 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.361-2225A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946891 | |||||||
chr15:39946974 | C | T | 1 | a0002c0002t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.361-2142C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946974 | |||||||
chr15:39947096 | C | T | 30 | a0002c0004t0001g0257 a0002c0004t0003g0256 a0002c0004t0003g0263 others(27): Show |
30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-2020C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947096 | |||||||
chr15:39947155 | T | C | 1 | a0001c0005t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.361-1961T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947155 | |||||||
chr15:39947258 | A | G | 52 | a0002c0011t0002g0096 a0003c0003t0001g0067 a0003c0003t0001g0073 others(49): Show |
52 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.361-1858A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947258 | |||||||
chr15:39947259 | T | G | 30 | a0002c0004t0001g0257 a0002c0004t0003g0256 a0002c0004t0003g0263 others(27): Show |
30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-1857T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947259 | |||||||
chr15:39947276 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(315): Show |
322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.361-1840A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947276 | |||||||
chr15:39947484 | G | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.361-1632G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947484 | |||||||
chr15:39947528 | G | A | 4 | a0002c0002t0003g0276 a0002c0004t0002g0272 a0002c0004t0002g0275 others(1): Show |
4 | HG00642.hp2 HG01884.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1588G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947528 | |||||||
chr15:39947575 | A | G | 65 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.361-1541A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947575 | |||||||
chr15:39947684 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.361-1432G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947684 | |||||||
chr15:39947711 | G | A | 75 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(72): Show |
76 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.361-1405G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947711 | |||||||
chr15:39947727 | A | G | 30 | a0002c0004t0001g0257 a0002c0004t0003g0256 a0002c0004t0003g0263 others(27): Show |
30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-1389A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947727 | |||||||
chr15:39947827 | G | C | 1 | a0001c0001t0003g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.361-1289G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947827 | |||||||
chr15:39947848 | TAGA | T | 3 | a0002c0002t0002g0336 a0002c0002t0002g0337 a0002c0002t0002g0338 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.361-1265_361-1263d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39947848 | ||||||
chr15:39947915 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.361-1201C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947915 | |||||||
chr15:39948343 | C | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(307): Show |
314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.361-773C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948343 | |||||||
chr15:39948358 | C | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361-758C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948358 | |||||||
chr15:39948687 | G | C | 9 | a0001c0001t0005g0014 a0001c0001t0005g0028 a0001c0001t0005g0029 others(6): Show |
9 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.361-429G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948687 | |||||||
chr15:39948861 | A | G | 1 | a0004c0007t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.361-255A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948861 | |||||||
chr15:39948936 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(62): Show |
67 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.361-180A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948936 | |||||||
chr15:39949401 | CAT | C | 4 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0234 others(1): Show |
4 | NA18964.hp1 NA18993.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+134_513+135del others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949401 | |||||||
chr15:39949644 | T | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(311): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.513+376T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949644 | |||||||
chr15:39949652 | T | C | 1 | a0002c0004t0001g0209 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.513+384T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949652 | |||||||
chr15:39949772 | T | TCAAAGAT others(5543): Show |
1 | a0001c0001t0003g0110 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.513+520_513+521ins others(5550): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39949772 | ||||||
chr15:39950048 | T | G | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.513+780T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950048 | |||||||
chr15:39950082 | T | C | 2 | a0002c0004t0001g0300 a0002c0004t0001g0345 |
2 | NA18969.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513+814T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950082 | |||||||
chr15:39950190 | A | G | 1 | a0002c0004t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.513+922A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950190 | |||||||
chr15:39950370 | A | C | 66 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.513+1102A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950370 | |||||||
chr15:39950510 | G | A | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1242G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950510 | |||||||
chr15:39950647 | G | A | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.513+1379G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950647 | |||||||
chr15:39950750 | CAT | C | 75 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(72): Show |
76 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.513+1483_513+1484d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950750 | |||||||
chr15:39950949 | A | G | 5 | a0002c0002t0002g0336 a0002c0002t0002g0337 a0002c0002t0002g0338 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1681A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950949 | |||||||
chr15:39950979 | T | C | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.513+1711T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950979 | |||||||
chr15:39951014 | A | G | 1 | a0002c0004t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.513+1746A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951014 | |||||||
chr15:39951027 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0004g0244 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513+1759G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951027 | |||||||
chr15:39951127 | T | C | 66 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.513+1859T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951127 | |||||||
chr15:39951207 | G | C | 8 | a0004c0006t0001g0210 a0004c0006t0002g0211 a0004c0007t0001g0212 others(5): Show |
8 | HG00544.hp2 HG00609.hp1 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1939G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951207 | |||||||
chr15:39951212 | A | C | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+1944A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951212 | |||||||
chr15:39951358 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(318): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.513+2090C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951358 | |||||||
chr15:39951375 | C | T | 1 | a0002c0002t0003g0276 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513+2107C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951375 | |||||||
chr15:39951459 | G | C | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.513+2191G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951459 | |||||||
chr15:39951623 | A | G | 1 | a0004c0007t0003g0258 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.514-2281A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951623 | |||||||
chr15:39951641 | A | G | 8 | a0001c0001t0005g0014 a0001c0001t0005g0028 a0001c0001t0005g0029 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-2263A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951641 | |||||||
chr15:39951714 | G | C | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2190G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951714 | |||||||
chr15:39951770 | T | G | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2134T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951770 | |||||||
chr15:39951822 | C | G | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.514-2082C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951822 | |||||||
chr15:39951832 | AC | A | 65 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.514-2067delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39951832 | ||||||
chr15:39951857 | A | G | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.514-2047A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951857 | |||||||
chr15:39951892 | C | G | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.514-2012C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951892 | |||||||
chr15:39952039 | C | T | 8 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-1865C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952039 | |||||||
chr15:39952294 | CT | C | 352 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(349): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.514-1596delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39952294 | ||||||
chr15:39952319 | C | T | 76 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(73): Show |
77 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.514-1585C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952319 | |||||||
chr15:39952321 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.514-1583T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952321 | |||||||
chr15:39952528 | A | G | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1376A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952528 | |||||||
chr15:39952580 | T | C | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1324T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952580 | |||||||
chr15:39952873 | A | C | 1 | a0002c0004t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.514-1031A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952873 | |||||||
chr15:39952897 | G | T | 77 | a0001c0001t0003g0218 a0002c0002t0001g0020 a0002c0002t0001g0022 others(74): Show |
78 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.514-1007G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952897 | |||||||
chr15:39952913 | T | C | 68 | a0001c0001t0003g0218 a0002c0002t0001g0359 a0002c0002t0001g0361 others(65): Show |
69 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.514-991T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952913 | |||||||
chr15:39953055 | C | T | 6 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0002c0002t0010g0046 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-849C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953055 | |||||||
chr15:39953128 | G | A | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.514-776G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953128 | |||||||
chr15:39953253 | C | G | 3 | a0003c0003t0002g0083 a0003c0003t0002g0084 a0003c0003t0002g0085 |
3 | NA18962.hp2 NA19004.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.514-651C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953253 | |||||||
chr15:39953517 | A | C | 1 | a0004c0007t0001g0216 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.514-387A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953517 | |||||||
chr15:39953553 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(204): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.514-351T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953553 | |||||||
chr15:39953578 | G | A | 34 | a0002c0002t0001g0003 a0002c0002t0001g0159 a0002c0002t0001g0160 others(31): Show |
37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.514-326G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953578 | |||||||
chr15:39953599 | G | A | 55 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(52): Show |
55 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.514-305G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953599 | |||||||
chr15:39953635 | A | C | 66 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.514-269A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953635 | |||||||
chr15:39953648 | A | G | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.514-256A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953648 | |||||||
chr15:39953725 | G | A | 35 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(32): Show |
35 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-179G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953725 | |||||||
chr15:39954101 | A | T | 1 | a0004c0007t0001g0216 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.594+117A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954101 | |||||||
chr15:39954172 | G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.594+188G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954172 | |||||||
chr15:39954188 | A | G | 8 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+204A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954188 | |||||||
chr15:39954236 | A | G | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.594+252A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954236 | |||||||
chr15:39954398 | G | A | 66 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0204 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.594+414G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954398 | |||||||
chr15:39954523 | G | A | 1 | a0002c0004t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.594+539G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954523 | |||||||
chr15:39954533 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(65): Show |
70 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.594+549C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954533 | |||||||
chr15:39954534 | G | A | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+550G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954534 | |||||||
chr15:39954867 | G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.595-753G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954867 | |||||||
chr15:39954996 | A | G | 3 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0011c0017t0002g0239 |
3 | HG02145.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.595-624A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954996 | |||||||
chr15:39955077 | C | A | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-543C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955077 | |||||||
chr15:39955166 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.595-454T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955166 | |||||||
chr15:39955262 | C | T | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-358C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955262 | |||||||
chr15:39955449 | C | G | 1 | a0003c0003t0002g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.595-171C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955449 | |||||||
chr15:39955488 | A | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(333): Show |
340 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.595-132A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955488 | |||||||
chr15:39955824 | A | G | 2 | a0003c0003t0001g0058 a0003c0003t0002g0059 |
2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.743+56A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955824 | |||||||
chr15:39955887 | A | G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.743+119A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955887 | |||||||
chr15:39955896 | ATCTT | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(65): Show |
70 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.743+129_743+132del others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955896 | |||||||
chr15:39955921 | G | A | 78 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(75): Show |
79 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.743+153G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955921 | |||||||
chr15:39956004 | CT | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(301): Show |
308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.743+255delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39956004 | ||||||
chr15:39956004 | CTT | C | 16 | a0001c0001t0003g0172 a0001c0001t0005g0028 a0001c0005t0001g0125 others(13): Show |
16 | HG00609.hp2 HG00741.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+254_743+255del others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39956004 | ||||||
chr15:39956131 | A | C | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+363A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956131 | |||||||
chr15:39956384 | A | G | 1 | a0002c0011t0002g0331 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.743+616A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956384 | |||||||
chr15:39956515 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(322): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.743+747T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956515 | |||||||
chr15:39956558 | A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.743+790A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956558 | |||||||
chr15:39956819 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(244): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.743+1051A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956819 | |||||||
chr15:39956846 | C | G | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+1078C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956846 | |||||||
chr15:39956882 | T | G | 1 | a0001c0001t0003g0217 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.743+1114T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956882 | |||||||
chr15:39956991 | A | T | 1 | a0002c0004t0004g0330 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.743+1223A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956991 | |||||||
chr15:39957021 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(322): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.743+1253T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957021 | |||||||
chr15:39957178 | C | T | 8 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.743+1410C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957178 | |||||||
chr15:39957325 | C | G | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+1557C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957325 | |||||||
chr15:39957464 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(260): Show |
266 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.743+1696C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957464 | |||||||
chr15:39957511 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(332): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.743+1743T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957511 | |||||||
chr15:39957565 | A | G | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.743+1797A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957565 | |||||||
chr15:39957646 | TG | T | 24 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.743+1879delG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957646 | |||||||
chr15:39957710 | A | T | 1 | a0013c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+1942A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957710 | |||||||
chr15:39957730 | A | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.743+1962A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957730 | |||||||
chr15:39957807 | A | G | 27 | a0004c0006t0001g0210 a0004c0006t0001g0254 a0004c0006t0001g0255 others(24): Show |
27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.743+2039A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957807 | |||||||
chr15:39957849 | G | C | 11 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0285 others(8): Show |
12 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2081G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957849 | |||||||
chr15:39958305 | T | C | 79 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(76): Show |
80 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.743+2537T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958305 | |||||||
chr15:39958331 | G | A | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+2563G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958331 | |||||||
chr15:39958476 | T | A | 79 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(76): Show |
80 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.743+2708T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958476 | |||||||
chr15:39958531 | G | C | 1 | a0005c0008t0001g0356 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.743+2763G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958531 | |||||||
chr15:39958550 | C | T | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.743+2782C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958550 | |||||||
chr15:39958587 | G | A | 1 | a0001c0001t0003g0268 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.743+2819G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958587 | |||||||
chr15:39958695 | C | T | 1 | a0002c0002t0002g0338 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.743+2927C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958695 | |||||||
chr15:39958736 | A | G | 3 | a0001c0001t0002g0219 a0001c0001t0002g0222 a0001c0005t0002g0220 |
3 | NA18950.hp1 NA19082.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.743+2968A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958736 | |||||||
chr15:39958800 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.744-2984A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958800 | |||||||
chr15:39958982 | G | A | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744-2802G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958982 | |||||||
chr15:39958996 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(256): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.744-2788T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958996 | |||||||
chr15:39958997 | G | A | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.744-2787G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958997 | |||||||
chr15:39959004 | T | G | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-2780T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959004 | |||||||
chr15:39959077 | A | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.744-2707A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959077 | |||||||
chr15:39959154 | C | T | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-2630C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959154 | |||||||
chr15:39959296 | G | C | 1 | a0002c0002t0010g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.744-2488G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959296 | |||||||
chr15:39959307 | A | C | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.744-2477A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959307 | |||||||
chr15:39959316 | G | A | 8 | a0003c0003t0002g0061 a0003c0003t0002g0062 a0003c0003t0002g0063 others(5): Show |
8 | HG01099.hp2 HG01109.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-2468G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959316 | |||||||
chr15:39959394 | T | C | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-2390T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959394 | |||||||
chr15:39959540 | A | G | 189 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0035 others(186): Show |
190 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.744-2244A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959540 | |||||||
chr15:39959714 | G | C | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.744-2070G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959714 | |||||||
chr15:39959731 | A | G | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-2053A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959731 | |||||||
chr15:39959850 | C | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.744-1934C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959850 | |||||||
chr15:39959901 | T | C | 4 | a0002c0002t0001g0285 a0002c0019t0001g0284 a0004c0006t0004g0248 others(1): Show |
4 | HG01074.hp2 HG01175.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-1883T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959901 | |||||||
chr15:39959930 | A | G | 10 | a0002c0004t0001g0005 a0002c0004t0001g0324 a0002c0004t0001g0325 others(7): Show |
11 | HG00642.hp1 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-1854A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959930 | |||||||
chr15:39959936 | G | C | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA19057.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.744-1848G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959936 | |||||||
chr15:39959959 | C | T | 8 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-1825C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959959 | |||||||
chr15:39959961 | A | C | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-1823A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959961 | |||||||
chr15:39959967 | G | T | 9 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(6): Show |
9 | HG01106.hp2 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.744-1817G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959967 | |||||||
chr15:39960011 | A | C | 115 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0002g0009 others(112): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.744-1773A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960011 | |||||||
chr15:39960129 | A | C | 78 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(75): Show |
79 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.744-1655A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960129 | |||||||
chr15:39960150 | C | T | 1 | a0004c0007t0002g0247 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.744-1634C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960150 | |||||||
chr15:39960163 | C | CAA | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-1602_744-1601d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39960163 | ||||||
chr15:39960273 | A | T | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-1511A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960273 | |||||||
chr15:39960308 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.744-1476A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960308 | |||||||
chr15:39960364 | A | G | 61 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.744-1420A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960364 | |||||||
chr15:39960470 | C | T | 190 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0035 others(187): Show |
191 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.744-1314C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960470 | |||||||
chr15:39960556 | G | C | 1 | a0001c0001t0003g0175 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.744-1228G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960556 | |||||||
chr15:39960584 | A | G | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-1200A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960584 | |||||||
chr15:39960766 | T | G | 1 | a0008c0015t0006g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.744-1018T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960766 | |||||||
chr15:39960923 | T | A | 76 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(73): Show |
77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.744-861T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960923 | |||||||
chr15:39961045 | C | A | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.744-739C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961045 | |||||||
chr15:39961139 | C | T | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-645C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961139 | |||||||
chr15:39961162 | A | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744-622A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961162 | |||||||
chr15:39961166 | A | G | 38 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0003g0161 others(35): Show |
38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.744-618A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961166 | |||||||
chr15:39961229 | C | T | 9 | a0002c0002t0003g0317 a0002c0002t0003g0318 a0002c0004t0001g0300 others(6): Show |
9 | NA18947.hp2 NA18949.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-555C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961229 | |||||||
chr15:39961262 | C | T | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-522C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961262 | |||||||
chr15:39961473 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.744-311G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961473 | |||||||
chr15:39961522 | C | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.744-262C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961522 | |||||||
chr15:39961542 | G | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.744-242G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961542 | |||||||
chr15:39961618 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.744-166C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961618 | |||||||
chr15:39961685 | G | A | 27 | a0004c0006t0001g0210 a0004c0006t0001g0254 a0004c0006t0001g0255 others(24): Show |
27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.744-99G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961685 | |||||||
chr15:39961758 | A | T | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.744-26A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961758 | |||||||
chr15:39961773 | T | G | 1 | a0004c0006t0004g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.744-11T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961773 | |||||||
chr15:39961954 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+55A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39961954 | |||||||
chr15:39961983 | C | G | 2 | a0004c0006t0001g0254 a0004c0006t0001g0255 |
2 | HG02698.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.859+84C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39961983 | |||||||
chr15:39962008 | A | G | 4 | a0002c0002t0007g0043 a0002c0004t0003g0039 a0009c0016t0007g0042 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+109A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962008 | |||||||
chr15:39962131 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+232T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962131 | |||||||
chr15:39962350 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(66): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.859+451G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962350 | |||||||
chr15:39962412 | G | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+513G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962412 | |||||||
chr15:39962745 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.859+846G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962745 | |||||||
chr15:39962852 | C | T | 24 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.859+953C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962852 | |||||||
chr15:39962955 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+1056A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962955 | |||||||
chr15:39962964 | T | G | 2 | a0003c0025t0004g0010 a0003c0026t0001g0011 |
2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859+1065T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962964 | |||||||
chr15:39963061 | C | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+1162C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963061 | |||||||
chr15:39963199 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.859+1300T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963199 | |||||||
chr15:39963229 | G | A | 27 | a0004c0006t0001g0210 a0004c0006t0001g0254 a0004c0006t0001g0255 others(24): Show |
27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.859+1330G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963229 | |||||||
chr15:39963544 | T | G | 1 | a0002c0002t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.859+1645T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963544 | |||||||
chr15:39963568 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.859+1669A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963568 | |||||||
chr15:39963659 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.859+1760A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963659 | |||||||
chr15:39963763 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.859+1864T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963763 | |||||||
chr15:39963843 | C | T | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1843C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963843 | |||||||
chr15:39963869 | A | T | 27 | a0004c0006t0001g0210 a0004c0006t0001g0254 a0004c0006t0001g0255 others(24): Show |
27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.860-1817A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963869 | |||||||
chr15:39964033 | T | C | 1 | a0002c0004t0001g0209 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.860-1653T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964033 | |||||||
chr15:39964123 | T | C | 33 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(30): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.860-1563T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964123 | |||||||
chr15:39964205 | A | G | 1 | a0002c0011t0002g0096 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.860-1481A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964205 | |||||||
chr15:39964235 | G | A | 76 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(73): Show |
77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.860-1451G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964235 | |||||||
chr15:39964268 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.860-1418A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964268 | |||||||
chr15:39964298 | A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.860-1388A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964298 | |||||||
chr15:39964400 | G | A | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1286G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964400 | |||||||
chr15:39964454 | TAA | T | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.860-1231_860-1230d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964454 | |||||||
chr15:39964470 | G | A | 76 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(73): Show |
77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.860-1216G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964470 | |||||||
chr15:39964502 | A | G | 5 | a0001c0001t0001g0204 a0001c0001t0003g0200 a0001c0001t0003g0201 others(2): Show |
5 | NA18970.hp2 NA18989.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.860-1184A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964502 | |||||||
chr15:39964541 | A | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0226 a0001c0005t0001g0225 |
4 | HG00099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1145A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964541 | |||||||
chr15:39964584 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.860-1102T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964584 | |||||||
chr15:39964774 | A | G | 74 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0002g0304 others(71): Show |
75 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.860-912A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964774 | |||||||
chr15:39964902 | T | C | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.860-784T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964902 | |||||||
chr15:39964993 | A | G | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.860-693A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964993 | |||||||
chr15:39965040 | T | C | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.860-646T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965040 | |||||||
chr15:39965156 | T | C | 1 | a0001c0005t0001g0152 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.860-530T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965156 | |||||||
chr15:39965161 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.860-525G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965161 | |||||||
chr15:39965312 | C | CG | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.860-370dupG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 39965312 | ||||||
chr15:39965316 | G | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(210): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.860-370G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965316 | |||||||
chr15:39965402 | G | A | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.860-284G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965402 | |||||||
chr15:39965404 | G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.860-282G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965404 | |||||||
chr15:39965413 | C | T | 3 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0002c0002t0010g0046 |
3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.860-273C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965413 | |||||||
chr15:39965414 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.860-272A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965414 | |||||||
chr15:39965544 | A | G | 1 | a0002c0004t0001g0320 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.860-142A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965544 | |||||||
chr15:39965559 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | NA18941.hp2 NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.860-127C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965559 | |||||||
chr15:39966127 | T | C | 2 | a0004c0007t0002g0266 a0004c0007t0003g0258 |
2 | NA18972.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1017+284T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966127 | |||||||
chr15:39966128 | A | C | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+285A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966128 | |||||||
chr15:39966349 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1017+506G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966349 | |||||||
chr15:39966430 | G | C | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+587G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966430 | |||||||
chr15:39966501 | C | CA | 220 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1017+671dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966501 | ||||||
chr15:39966501 | C | CAA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(69): Show |
74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1017+670_1017+671d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966501 | ||||||
chr15:39966765 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1018-579A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966765 | |||||||
chr15:39966793 | A | G | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018-551A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966793 | |||||||
chr15:39966828 | A | G | 7 | a0003c0003t0002g0078 a0003c0003t0002g0080 a0003c0003t0002g0081 others(4): Show |
7 | HG00621.hp2 NA18612.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018-516A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966828 | |||||||
chr15:39966840 | AT | A | 63 | a0001c0001t0001g0169 a0001c0001t0001g0206 a0001c0001t0001g0243 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1018-494delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966840 | ||||||
chr15:39966853 | G | A | 76 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(73): Show |
77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1018-491G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966853 | |||||||
chr15:39967303 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1018-41G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39967303 | |||||||
chr15:39967318 | C | CT | 273 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(270): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1018-11dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39967318 | ||||||
chr15:39967318 | C | CTT | 40 | a0002c0002t0001g0003 a0002c0002t0001g0035 a0002c0002t0001g0270 others(37): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1018-12_1018-11dup others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39967318 | ||||||
chr15:39968007 | C | T | 53 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(50): Show |
53 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1553+128C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968007 | |||||||
chr15:39968015 | G | A | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1553+136G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968015 | |||||||
chr15:39968122 | G | A | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+243G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968122 | |||||||
chr15:39968210 | G | C | 1 | a0013c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1553+331G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968210 | |||||||
chr15:39968230 | G | C | 1 | a0005c0014t0004g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+351G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968230 | |||||||
chr15:39968287 | A | G | 5 | a0001c0005t0001g0125 a0001c0005t0005g0123 a0001c0005t0005g0124 others(2): Show |
5 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553+408A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968287 | |||||||
chr15:39968313 | A | G | 1 | a0007c0009t0003g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1553+434A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968313 | |||||||
chr15:39968341 | C | T | 1 | a0005c0014t0004g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+462C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968341 | |||||||
chr15:39968369 | C | A | 38 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0003g0161 others(35): Show |
38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1553+490C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968369 | |||||||
chr15:39968451 | C | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1553+572C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968451 | |||||||
chr15:39968507 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1553+628T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968507 | |||||||
chr15:39968545 | C | A | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+666C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968545 | |||||||
chr15:39968745 | A | G | 38 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0003g0161 others(35): Show |
38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1553+866A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968745 | |||||||
chr15:39968824 | G | A | 1 | a0002c0011t0002g0301 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1553+945G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968824 | |||||||
chr15:39968873 | G | GAT | 6 | a0002c0004t0001g0041 a0003c0003t0001g0106 a0003c0003t0002g0054 others(3): Show |
6 | HG00673.hp1 HG02165.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1553+1012_1553+101 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATAT | 15 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(12): Show |
15 | HG01255.hp1 HG01891.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1553+1010_1553+101 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATATAT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(60): Show |
65 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1553+1008_1553+101 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATATATA others(1): Show |
9 | a0001c0001t0002g0118 a0001c0001t0002g0148 a0001c0001t0002g0151 others(6): Show |
9 | HG02129.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+1006_1553+101 others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATATATA others(3): Show |
19 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0004c0006t0001g0254 others(16): Show |
19 | HG01074.hp2 HG01106.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1553+1004_1553+101 others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATATATA others(5): Show |
9 | a0002c0002t0003g0335 a0004c0006t0001g0259 a0004c0006t0002g0211 others(6): Show |
9 | HG00544.hp2 HG01168.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+1002_1553+101 others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968873 | G | GATATATA others(7): Show |
1 | a0004c0007t0001g0215 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1553+1000_1553+101 others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | ||||||
chr15:39968891 | T | TATAC | 92 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(89): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | ||||||
chr15:39968891 | T | TATATAC | 4 | a0001c0001t0003g0175 a0002c0002t0001g0290 a0005c0008t0004g0004 others(1): Show |
5 | HG00140.hp1 HG01361.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | ||||||
chr15:39968891 | T | TATATATA others(3): Show |
6 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0004g0236 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | ||||||
chr15:39968891 | T | TATATATA others(5): Show |
3 | a0004c0006t0001g0210 a0010c0018t0005g0238 a0010c0018t0005g0240 |
3 | HG00609.hp1 HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | ||||||
chr15:39969065 | C | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1553+1186C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969065 | |||||||
chr15:39969078 | T | C | 55 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(52): Show |
55 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1553+1199T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969078 | |||||||
chr15:39969097 | A | G | 3 | a0002c0002t0001g0035 a0002c0004t0003g0038 a0002c0004t0003g0039 |
3 | HG02630.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1553+1218A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969097 | |||||||
chr15:39969227 | A | G | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1348A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969227 | |||||||
chr15:39969345 | A | T | 2 | a0003c0003t0002g0076 a0003c0010t0001g0077 |
2 | NA19056.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1553+1466A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969345 | |||||||
chr15:39969356 | C | CT | 78 | a0001c0001t0003g0198 a0002c0002t0001g0020 a0002c0002t0001g0022 others(75): Show |
79 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1553+1499dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | ||||||
chr15:39969356 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(79): Show |
84 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1553+1499delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | ||||||
chr15:39969356 | CTT | C | 41 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0031 others(38): Show |
41 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1553+1498_1553+149 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | ||||||
chr15:39969356 | CTTTTTT | C | 54 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(51): Show |
54 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1553+1494_1553+149 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | ||||||
chr15:39969423 | C | T | 1 | a0003c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1553+1544C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969423 | |||||||
chr15:39969477 | C | G | 1 | a0004c0006t0002g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1553+1598C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969477 | |||||||
chr15:39969522 | G | A | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1643G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969522 | |||||||
chr15:39969529 | G | T | 1 | a0003c0003t0002g0095 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1553+1650G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969529 | |||||||
chr15:39969554 | G | A | 14 | a0003c0003t0001g0099 a0003c0003t0002g0052 a0003c0003t0002g0053 others(11): Show |
14 | HG01346.hp2 HG01981.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1553+1675G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969554 | |||||||
chr15:39969651 | C | T | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1553+1772C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969651 | |||||||
chr15:39969701 | A | G | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553+1822A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969701 | |||||||
chr15:39969811 | T | C | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1553+1932T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969811 | |||||||
chr15:39970074 | G | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(295): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1553+2195G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970074 | |||||||
chr15:39970123 | A | G | 1 | a0004c0006t0002g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1553+2244A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970123 | |||||||
chr15:39970128 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1553+2249C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970128 | |||||||
chr15:39970215 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1553+2336C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970215 | |||||||
chr15:39970263 | A | G | 27 | a0004c0006t0001g0210 a0004c0006t0001g0254 a0004c0006t0001g0255 others(24): Show |
27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1553+2384A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970263 | |||||||
chr15:39970300 | T | G | 3 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0002c0002t0010g0046 |
3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1553+2421T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970300 | |||||||
chr15:39970358 | A | G | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1553+2479A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970358 | |||||||
chr15:39970482 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1554-2426G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970482 | |||||||
chr15:39970490 | G | C | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1554-2418G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970490 | |||||||
chr15:39970530 | A | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1554-2378A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970530 | |||||||
chr15:39970617 | A | C | 4 | a0002c0002t0001g0270 a0002c0002t0001g0285 a0002c0002t0001g0360 others(1): Show |
4 | HG00140.hp2 HG01081.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-2291A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970617 | |||||||
chr15:39970647 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1554-2261T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970647 | |||||||
chr15:39970789 | G | A | 53 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(50): Show |
53 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1554-2119G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970789 | |||||||
chr15:39970790 | C | T | 2 | a0002c0002t0004g0018 a0002c0002t0004g0019 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1554-2118C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970790 | |||||||
chr15:39970881 | A | G | 2 | a0002c0004t0002g0272 a0002c0004t0002g0353 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1554-2027A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970881 | |||||||
chr15:39970915 | G | A | 70 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0002g0304 others(67): Show |
71 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1554-1993G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970915 | |||||||
chr15:39971161 | T | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1554-1747T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971161 | |||||||
chr15:39971172 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(290): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1554-1736T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971172 | |||||||
chr15:39971250 | G | A | 2 | a0001c0005t0005g0153 a0006c0032t0005g0122 |
2 | HG00741.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1554-1658G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971250 | |||||||
chr15:39971262 | A | C | 3 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0005g0021 |
3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1554-1646A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971262 | |||||||
chr15:39971357 | C | G | 1 | a0004c0006t0002g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1554-1551C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971357 | |||||||
chr15:39971402 | T | C | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1554-1506T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971402 | |||||||
chr15:39971498 | T | G | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1554-1410T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971498 | |||||||
chr15:39971506 | G | C | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1554-1402G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971506 | |||||||
chr15:39971564 | C | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1554-1344C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971564 | |||||||
chr15:39971628 | G | T | 1 | a0005c0008t0004g0339 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1554-1280G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971628 | |||||||
chr15:39971716 | C | CA | 38 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0003g0161 others(35): Show |
38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1554-1181dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39971716 | ||||||
chr15:39971720 | A | C | 1 | a0003c0003t0002g0081 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1554-1188A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971720 | |||||||
chr15:39972036 | T | A | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1554-872T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972036 | |||||||
chr15:39972180 | G | A | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1554-728G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972180 | |||||||
chr15:39972290 | G | A | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1554-618G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972290 | |||||||
chr15:39972328 | C | T | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1554-580C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972328 | |||||||
chr15:39972349 | C | CA | 38 | a0001c0001t0002g0205 a0001c0021t0003g0223 a0002c0002t0001g0003 others(35): Show |
41 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1554-544dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39972349 | ||||||
chr15:39972381 | A | T | 1 | a0002c0002t0001g0285 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1554-527A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972381 | |||||||
chr15:39972544 | T | C | 4 | a0002c0002t0004g0236 a0002c0004t0005g0237 a0010c0018t0005g0238 others(1): Show |
4 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-364T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972544 | |||||||
chr15:39972649 | G | A | 1 | a0002c0004t0002g0316 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1554-259G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972649 | |||||||
chr15:39972804 | A | G | 1 | a0001c0005t0005g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1554-104A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972804 | |||||||
chr15:39973023 | G | A | 1 | a0002c0002t0002g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1660+9G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973023 | |||||||
chr15:39973026 | A | T | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1660+12A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973026 | |||||||
chr15:39973109 | T | G | 56 | a0002c0004t0014g0302 a0003c0003t0001g0058 a0003c0003t0001g0067 others(53): Show |
56 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1660+95T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973109 | |||||||
chr15:39973203 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(289): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1660+189T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973203 | |||||||
chr15:39973238 | T | C | 2 | a0002c0004t0002g0272 a0002c0004t0002g0353 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1660+224T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973238 | |||||||
chr15:39973255 | T | C | 1 | a0002c0002t0002g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1660+241T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973255 | |||||||
chr15:39973302 | C | A | 74 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(71): Show |
75 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+288C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973302 | |||||||
chr15:39973387 | C | T | 74 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(71): Show |
75 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-205C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973387 | |||||||
chr15:39973535 | T | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1661-57T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973535 | |||||||
chr15:39973543 | C | T | 1 | a0002c0011t0002g0346 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1661-49C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973543 | |||||||
chr15:39974042 | T | G | 1 | a0002c0004t0001g0321 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1818+293T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974042 | |||||||
chr15:39974075 | T | C | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1818+326T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974075 | |||||||
chr15:39974334 | T | C | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1818+585T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974334 | |||||||
chr15:39974625 | C | T | 1 | a0002c0002t0001g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1818+876C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974625 | |||||||
chr15:39974635 | C | T | 38 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0002c0002t0003g0161 others(35): Show |
38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1818+886C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974635 | |||||||
chr15:39974761 | T | C | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1818+1012T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974761 | |||||||
chr15:39974909 | G | A | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1818+1160G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974909 | |||||||
chr15:39975046 | C | G | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1818+1297C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975046 | |||||||
chr15:39975174 | C | T | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1819-1240C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975174 | |||||||
chr15:39975246 | A | ATGACACA others(7): Show |
295 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1819-1167_1819-116 others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr15 | 39975246 | ||||||
chr15:39975328 | AAGAT | A | 78 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(75): Show |
79 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1819-1084_1819-108 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr15 | 39975328 | ||||||
chr15:39975342 | C | G | 33 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(30): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1819-1072C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975342 | |||||||
chr15:39975526 | A | C | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1819-888A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975526 | |||||||
chr15:39975736 | A | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | NA18941.hp2 NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1819-678A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975736 | |||||||
chr15:39976013 | G | A | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1819-401G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976013 | |||||||
chr15:39976058 | C | G | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1819-356C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976058 | |||||||
chr15:39976148 | A | G | 1 | a0002c0004t0002g0348 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1819-266A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976148 | |||||||
chr15:39976225 | G | C | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1819-189G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976225 | |||||||
chr15:39976343 | G | A | 57 | a0003c0003t0001g0058 a0003c0003t0001g0067 a0003c0003t0001g0073 others(54): Show |
57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1819-71G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976343 | |||||||
chr15:39976851 | G | A | 80 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(77): Show |
81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
splice_region_variant&intron_variant | LOW | c.2249+7G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976851 | |||||||
chr15:39976878 | G | T | 64 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2249+34G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976878 | |||||||
chr15:39976901 | A | AT | 81 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0359 others(78): Show |
82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.2249+66dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39976901 | ||||||
chr15:39976925 | T | TTTCC | 213 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(210): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2249+93_2249+96dup others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39976925 | ||||||
chr15:39976946 | T | C | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+102T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976946 | |||||||
chr15:39977131 | T | TCAAAAA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2249+287_2249+288i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977131 | |||||||
chr15:39977132 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2249+288T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977132 | |||||||
chr15:39977132 | T | TAAAAAC | 33 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0004c0006t0001g0210 others(30): Show |
33 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.2249+305_2249+310d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977132 | ||||||
chr15:39977132 | T | TAAAAACA others(5): Show |
2 | a0002c0002t0004g0236 a0002c0004t0005g0237 |
2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2249+299_2249+310d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977132 | ||||||
chr15:39977149 | A | G | 2 | a0003c0003t0001g0058 a0003c0003t0002g0059 |
2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2249+305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977149 | |||||||
chr15:39977151 | A | AAAAACG | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+310_2249+311i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977151 | ||||||
chr15:39977161 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2249+317C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977161 | |||||||
chr15:39977300 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(210): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2249+456C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977300 | |||||||
chr15:39977397 | A | G | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+553A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977397 | |||||||
chr15:39977410 | G | A | 9 | a0002c0002t0001g0035 a0002c0002t0002g0040 a0002c0002t0007g0043 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2249+566G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977410 | |||||||
chr15:39977482 | AGGCAGTG others(5): Show |
A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(210): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2250-594_2250-583d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977482 | ||||||
chr15:39977599 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(289): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2250-479T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977599 | |||||||
chr15:39977612 | T | G | 1 | a0003c0003t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2250-466T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977612 | |||||||
chr15:39977642 | A | G | 158 | a0002c0002t0001g0003 a0002c0002t0001g0020 a0002c0002t0001g0022 others(155): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2250-436A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977642 | |||||||
chr15:39977715 | T | C | 2 | a0002c0004t0001g0321 a0002c0004t0001g0322 |
2 | HG01256.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2250-363T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977715 | |||||||
chr15:39977722 | C | T | 1 | a0004c0006t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2250-356C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977722 | |||||||
chr15:39977845 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2250-233C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977845 | |||||||
chr15:39977846 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2250-232A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977846 | |||||||
chr15:39977950 | C | T | 6 | a0003c0003t0002g0230 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-128C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977950 | |||||||
chr15:39978013 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2250-65A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39978013 | |||||||
chr15:39978220 | A | G | 3 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0005g0021 |
3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2319+73A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978220 | |||||||
chr15:39978437 | A | G | 54 | a0002c0004t0014g0302 a0003c0003t0001g0058 a0003c0003t0001g0067 others(51): Show |
54 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2319+290A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978437 | |||||||
chr15:39978454 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(66): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2319+307T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978454 | |||||||
chr15:39978505 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(66): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2319+358G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978505 | |||||||
chr15:39978505 | G | T | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2319+358G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978505 | |||||||
chr15:39978595 | G | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2319+448G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978595 | |||||||
chr15:39978743 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(214): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2319+596T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978743 | |||||||
chr15:39978801 | T | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2319+654T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978801 | |||||||
chr15:39978923 | A | G | 3 | a0003c0003t0002g0083 a0003c0003t0002g0084 a0003c0003t0002g0085 |
3 | NA18962.hp2 NA19004.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2319+776A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978923 | |||||||
chr15:39979001 | A | G | 28 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(25): Show |
31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.2319+854A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979001 | |||||||
chr15:39979003 | C | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2319+856C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979003 | |||||||
chr15:39979053 | T | G | 1 | a0002c0002t0004g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2319+906T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979053 | |||||||
chr15:39979070 | A | G | 34 | a0001c0001t0001g0355 a0002c0002t0003g0161 a0002c0002t0003g0334 others(31): Show |
34 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.2319+923A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979070 | |||||||
chr15:39979080 | G | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(62): Show |
67 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2319+933G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979080 | |||||||
chr15:39979102 | C | T | 70 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0002c0002t0001g0359 others(67): Show |
71 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.2319+955C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979102 | |||||||
chr15:39979256 | G | A | 84 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0002c0002t0001g0020 others(81): Show |
85 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.2319+1109G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979256 | |||||||
chr15:39979536 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(164): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2319+1389G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979536 | |||||||
chr15:39979560 | T | C | 2 | a0001c0001t0003g0245 a0001c0005t0001g0246 |
2 | HG01081.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2319+1413T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979560 | |||||||
chr15:39979661 | C | T | 2 | a0002c0004t0001g0300 a0002c0004t0001g0345 |
2 | NA18969.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2319+1514C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979661 | |||||||
chr15:39979734 | A | G | 63 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2319+1587A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979734 | |||||||
chr15:39979760 | C | G | 5 | a0001c0001t0002g0090 a0001c0001t0002g0120 a0001c0001t0002g0145 others(2): Show |
5 | HG00438.hp2 HG02129.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+1613C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979760 | |||||||
chr15:39979773 | C | T | 1 | a0001c0022t0002g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2319+1626C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979773 | |||||||
chr15:39979831 | C | T | 75 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2319+1684C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979831 | |||||||
chr15:39979947 | C | T | 114 | a0001c0001t0001g0355 a0001c0005t0001g0032 a0001c0005t0001g0034 others(111): Show |
115 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2319+1800C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979947 | |||||||
chr15:39979948 | G | A | 1 | a0003c0003t0002g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2319+1801G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979948 | |||||||
chr15:39979978 | A | G | 1 | a0004c0006t0003g0344 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2319+1831A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979978 | |||||||
chr15:39980056 | A | C | 3 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0002c0002t0010g0046 |
3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2319+1909A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980056 | |||||||
chr15:39980153 | A | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2319+2006A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980153 | |||||||
chr15:39980154 | A | G | 1 | a0002c0019t0001g0281 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2319+2007A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980154 | |||||||
chr15:39980190 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(220): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2319+2043G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980190 | |||||||
chr15:39980217 | A | G | 1 | a0003c0003t0002g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2319+2070A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980217 | |||||||
chr15:39980219 | G | A | 5 | a0001c0005t0001g0125 a0001c0005t0005g0123 a0001c0005t0005g0124 others(2): Show |
5 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+2072G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980219 | |||||||
chr15:39980222 | C | T | 2 | a0003c0003t0002g0098 a0003c0003t0002g0102 |
2 | HG01346.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2319+2075C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980222 | |||||||
chr15:39980348 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0154 |
2 | HG02027.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2319+2201C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980348 | |||||||
chr15:39980515 | A | G | 3 | a0001c0001t0002g0138 a0003c0003t0001g0058 a0003c0003t0002g0059 |
3 | HG02647.hp2 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2319+2368A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980515 | |||||||
chr15:39980634 | C | T | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+2487C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980634 | |||||||
chr15:39980657 | T | G | 1 | a0002c0029t0002g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2319+2510T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980657 | |||||||
chr15:39980829 | T | C | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2319+2682T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980829 | |||||||
chr15:39981185 | C | G | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+3038C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981185 | |||||||
chr15:39981273 | G | T | 3 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0011c0017t0002g0239 |
3 | HG02145.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2319+3126G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981273 | |||||||
chr15:39981327 | G | A | 10 | a0001c0005t0001g0137 a0001c0005t0001g0152 a0004c0006t0001g0210 others(7): Show |
10 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2319+3180G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981327 | |||||||
chr15:39981436 | G | A | 20 | a0001c0001t0001g0355 a0002c0002t0001g0020 a0002c0002t0001g0022 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2319+3289G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981436 | |||||||
chr15:39981573 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2319+3426T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981573 | |||||||
chr15:39981587 | C | T | 72 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0001c0005t0005g0108 others(69): Show |
72 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2319+3440C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981587 | |||||||
chr15:39981608 | CT | C | 84 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2319+3473delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981608 | ||||||
chr15:39981613 | T | C | 62 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(59): Show |
62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2319+3466T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981613 | |||||||
chr15:39981624 | T | C | 1 | a0001c0001t0005g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2319+3477T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981624 | |||||||
chr15:39981649 | T | C | 9 | a0001c0005t0005g0108 a0002c0002t0002g0241 a0002c0002t0002g0242 others(6): Show |
9 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2319+3502T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981649 | |||||||
chr15:39981699 | T | C | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2319+3552T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981699 | |||||||
chr15:39981742 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(167): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2319+3595T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981742 | |||||||
chr15:39981813 | A | C | 1 | a0002c0002t0001g0290 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2319+3666A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981813 | |||||||
chr15:39981842 | T | G | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2319+3695T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981842 | |||||||
chr15:39981924 | C | CT | 12 | a0001c0005t0005g0108 a0002c0002t0002g0241 a0002c0002t0002g0242 others(9): Show |
12 | HG00544.hp2 HG01175.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.2319+3796dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | ||||||
chr15:39981924 | C | CTT | 76 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2319+3795_2319+379 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | ||||||
chr15:39981924 | C | CTTT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(85): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2319+3794_2319+379 others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | ||||||
chr15:39981924 | C | CTTTT | 7 | a0001c0001t0001g0133 a0001c0001t0001g0154 a0001c0001t0002g0119 others(4): Show |
7 | HG02055.hp2 HG02074.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.2319+3793_2319+379 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | ||||||
chr15:39981924 | CT | C | 62 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(59): Show |
62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2319+3796delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | ||||||
chr15:39981988 | G | A | 1 | a0012c0028t0002g0307 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2320-3817G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981988 | |||||||
chr15:39982049 | C | T | 1 | a0002c0004t0003g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2320-3756C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982049 | |||||||
chr15:39982115 | A | G | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3690A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982115 | |||||||
chr15:39982125 | C | T | 2 | a0003c0003t0001g0058 a0003c0003t0002g0059 |
2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2320-3680C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982125 | |||||||
chr15:39982172 | C | A | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-3633C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982172 | |||||||
chr15:39982188 | T | G | 1 | a0002c0002t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2320-3617T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982188 | |||||||
chr15:39982399 | A | C | 1 | a0003c0003t0004g0074 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2320-3406A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982399 | |||||||
chr15:39982526 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2320-3279T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982526 | |||||||
chr15:39982538 | TTTTTC | T | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-3252_2320-324 others(9): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39982538 | ||||||
chr15:39982605 | T | C | 11 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(8): Show |
11 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2320-3200T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982605 | |||||||
chr15:39982616 | A | G | 62 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2320-3189A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982616 | |||||||
chr15:39982617 | C | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3188C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982617 | |||||||
chr15:39982618 | A | C | 1 | a0002c0004t0001g0319 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2320-3187A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982618 | |||||||
chr15:39982633 | G | GT | 264 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2320-3170dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39982633 | ||||||
chr15:39982693 | C | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3112C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982693 | |||||||
chr15:39982708 | C | A | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3097C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982708 | |||||||
chr15:39982709 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2320-3096T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982709 | |||||||
chr15:39982780 | A | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3025A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982780 | |||||||
chr15:39982840 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2320-2965T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982840 | |||||||
chr15:39982956 | T | G | 2 | a0001c0001t0001g0243 a0001c0001t0004g0244 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2320-2849T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982956 | |||||||
chr15:39983088 | A | G | 2 | a0002c0004t0001g0321 a0002c0004t0001g0322 |
2 | HG01256.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2320-2717A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983088 | |||||||
chr15:39983115 | T | C | 8 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 others(5): Show |
8 | HG02451.hp2 HG02622.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-2690T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983115 | |||||||
chr15:39983163 | T | A | 83 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2320-2642T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983163 | |||||||
chr15:39983201 | G | A | 3 | a0002c0004t0001g0005 a0002c0004t0001g0325 a0002c0004t0001g0326 |
4 | HG00741.hp2 HG01069.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2320-2604G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983201 | |||||||
chr15:39983447 | CT | C | 162 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2320-2346delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39983447 | ||||||
chr15:39983592 | G | A | 1 | a0002c0002t0005g0292 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2320-2213G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983592 | |||||||
chr15:39983652 | G | A | 14 | a0001c0001t0001g0355 a0004c0006t0001g0254 a0004c0006t0001g0255 others(11): Show |
14 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.2320-2153G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983652 | |||||||
chr15:39983693 | C | T | 23 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(20): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.2320-2112C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983693 | |||||||
chr15:39983694 | G | A | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-2111G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983694 | |||||||
chr15:39983732 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(59): Show |
64 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2320-2073G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983732 | |||||||
chr15:39983733 | C | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-2072C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983733 | |||||||
chr15:39984033 | G | A | 1 | a0003c0003t0002g0230 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2320-1772G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984033 | |||||||
chr15:39984226 | C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2320-1579C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984226 | |||||||
chr15:39984371 | TTTCCTAA | T | 3 | a0002c0004t0001g0257 a0002c0004t0003g0256 a0002c0004t0003g0263 |
3 | HG00544.hp1 HG02135.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2320-1430_2320-142 others(11): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39984371 | ||||||
chr15:39984685 | T | C | 27 | a0002c0002t0001g0003 a0002c0002t0001g0270 a0002c0002t0001g0283 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.2320-1120T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984685 | |||||||
chr15:39984770 | C | T | 83 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2320-1035C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984770 | |||||||
chr15:39984871 | A | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2320-934A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984871 | |||||||
chr15:39985017 | A | C | 105 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2320-788A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985017 | |||||||
chr15:39985255 | A | G | 62 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(59): Show |
62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2320-550A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985255 | |||||||
chr15:39985383 | C | T | 105 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2320-422C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985383 | |||||||
chr15:39985402 | G | A | 60 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(57): Show |
60 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2320-403G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985402 | |||||||
chr15:39985508 | C | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2320-297C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985508 | |||||||
chr15:39985651 | T | G | 1 | a0002c0004t0004g0330 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2320-154T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985651 | |||||||
chr15:39985703 | G | A | 11 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 others(8): Show |
11 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2320-102G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985703 | |||||||
chr15:39985801 | T | G | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2320-4T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985801 | |||||||
chr15:39985900 | G | A | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39985900 | |||||||
chr15:39985991 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2403+103T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39985991 | |||||||
chr15:39986011 | T | C | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+123T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986011 | |||||||
chr15:39986017 | G | A | 3 | a0002c0002t0002g0308 a0002c0002t0002g0309 a0002c0002t0002g0310 |
3 | HG03139.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2403+129G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986017 | |||||||
chr15:39986025 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2403+137T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986025 | |||||||
chr15:39986201 | CTATA | C | 6 | a0001c0005t0005g0108 a0002c0002t0004g0236 a0002c0004t0005g0237 others(3): Show |
6 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+314_2403+317d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986201 | |||||||
chr15:39986205 | A | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2403+317A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986205 | |||||||
chr15:39986208 | T | G | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+320T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986208 | |||||||
chr15:39986283 | A | G | 1 | a0002c0004t0002g0353 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2403+395A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986283 | |||||||
chr15:39986367 | G | T | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2403+479G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986367 | |||||||
chr15:39986821 | CT | C | 7 | a0001c0005t0001g0134 a0001c0005t0001g0135 a0001c0005t0004g0121 others(4): Show |
7 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+934delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986821 | |||||||
chr15:39986877 | C | CAAA | 62 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(59): Show |
62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2403+991_2403+992i others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr15 | 39986877 | ||||||
chr15:39986880 | C | A | 67 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0002c0004t0014g0302 others(64): Show |
67 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.2403+992C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986880 | |||||||
chr15:39986880 | C | CAACA | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+994_2403+995i others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr15 | 39986880 | ||||||
chr15:39987086 | G | A | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-897G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987086 | |||||||
chr15:39987117 | A | G | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-866A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987117 | |||||||
chr15:39987244 | T | C | 2 | a0002c0002t0002g0350 a0002c0002t0002g0351 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2404-739T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987244 | |||||||
chr15:39987261 | G | A | 63 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2404-722G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987261 | |||||||
chr15:39987274 | C | T | 1 | a0002c0002t0002g0310 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-709C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987274 | |||||||
chr15:39987317 | T | C | 8 | a0002c0002t0002g0040 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404-666T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987317 | |||||||
chr15:39987380 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2404-603A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987380 | |||||||
chr15:39987579 | T | C | 10 | a0001c0005t0001g0137 a0001c0005t0001g0152 a0004c0006t0001g0210 others(7): Show |
10 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2404-404T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987579 | |||||||
chr15:39987775 | A | G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2404-208A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987775 | |||||||
chr15:39988296 | T | G | 1 | a0003c0003t0002g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2526+191T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988296 | |||||||
chr15:39988338 | G | A | 20 | a0001c0001t0001g0355 a0002c0002t0001g0020 a0002c0002t0001g0022 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2526+233G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988338 | |||||||
chr15:39988415 | C | T | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2526+310C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988415 | |||||||
chr15:39988492 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(222): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2526+387G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988492 | |||||||
chr15:39988527 | T | C | 2 | a0001c0001t0003g0178 a0001c0001t0003g0179 |
2 | NA18965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2526+422T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988527 | |||||||
chr15:39988536 | A | G | 2 | a0001c0001t0003g0202 a0001c0001t0003g0203 |
2 | NA19001.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2526+431A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988536 | |||||||
chr15:39988565 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(229): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2526+460C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988565 | |||||||
chr15:39988592 | G | T | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526+487G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988592 | |||||||
chr15:39988636 | A | G | 1 | a0001c0001t0011g0163 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2526+531A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988636 | |||||||
chr15:39988642 | G | A | 3 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0002c0002t0010g0046 |
3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2526+537G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988642 | |||||||
chr15:39988817 | A | G | 20 | a0001c0001t0001g0355 a0002c0002t0001g0020 a0002c0002t0001g0022 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2526+712A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988817 | |||||||
chr15:39988852 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0002g0128 |
2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2526+747T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988852 | |||||||
chr15:39988895 | G | A | 3 | a0001c0001t0002g0117 a0001c0001t0002g0140 a0001c0001t0002g0177 |
3 | HG00673.hp2 HG02071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2526+790G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988895 | |||||||
chr15:39989058 | A | T | 61 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0003c0003t0001g0058 others(58): Show |
61 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2526+953A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989058 | |||||||
chr15:39989275 | A | C | 3 | a0003c0003t0001g0343 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2527-998A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989275 | |||||||
chr15:39989276 | A | G | 10 | a0001c0005t0005g0108 a0002c0002t0002g0241 a0002c0002t0002g0242 others(7): Show |
10 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2527-997A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989276 | |||||||
chr15:39989337 | T | C | 91 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0206 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2527-936T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989337 | |||||||
chr15:39989466 | G | A | 5 | a0001c0005t0005g0108 a0002c0002t0004g0236 a0002c0004t0005g0237 others(2): Show |
5 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2527-807G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989466 | |||||||
chr15:39989483 | T | C | 20 | a0001c0001t0001g0355 a0002c0002t0001g0020 a0002c0002t0001g0022 others(17): Show |
20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2527-790T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989483 | |||||||
chr15:39989571 | A | G | 59 | a0001c0001t0002g0138 a0001c0001t0002g0147 a0003c0003t0001g0058 others(56): Show |
59 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.2527-702A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989571 | |||||||
chr15:39989650 | C | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2527-623C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989650 | |||||||
chr15:39990122 | A | G | 3 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0005g0021 |
3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2527-151A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39990122 | |||||||
chr15:39990180 | A | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2527-93A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39990180 | |||||||
chr15:39990404 | C | T | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | NA18943.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2631+27C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990404 | |||||||
chr15:39990424 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(341): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2631+47T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990424 | |||||||
chr15:39990500 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2631+123T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990500 | |||||||
chr15:39990530 | T | C | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2631+153T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990530 | |||||||
chr15:39990739 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2631+362G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990739 | |||||||
chr15:39990862 | G | A | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2631+485G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990862 | |||||||
chr15:39990898 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(77): Show |
84 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2631+521A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990898 | |||||||
chr15:39990998 | G | A | 1 | a0002c0004t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2631+621G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990998 | |||||||
chr15:39991049 | T | C | 154 | a0001c0001t0001g0204 a0001c0001t0002g0013 a0001c0001t0002g0111 others(151): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2631+672T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991049 | |||||||
chr15:39991053 | A | G | 68 | a0001c0001t0001g0204 a0001c0001t0002g0013 a0001c0001t0002g0111 others(65): Show |
69 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2631+676A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991053 | |||||||
chr15:39991073 | G | A | 187 | a0001c0001t0001g0204 a0001c0001t0001g0355 a0001c0001t0002g0013 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2631+696G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991073 | |||||||
chr15:39991248 | C | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(335): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2631+871C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991248 | |||||||
chr15:39991258 | C | T | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2631+881C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991258 | |||||||
chr15:39991500 | G | A | 2 | a0002c0002t0001g0359 a0002c0031t0009g0045 |
2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2632-675G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991500 | |||||||
chr15:39991573 | A | G | 1 | a0004c0007t0003g0258 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2632-602A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991573 | |||||||
chr15:39991596 | T | G | 91 | a0001c0001t0001g0243 a0001c0001t0002g0177 a0001c0005t0001g0125 others(88): Show |
92 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2632-579T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991596 | |||||||
chr15:39991918 | C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2632-257C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991918 | |||||||
chr15:39992007 | T | A | 8 | a0005c0008t0001g0296 a0005c0008t0001g0298 a0005c0008t0001g0356 others(5): Show |
10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2632-168T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39992007 | |||||||
chr15:39992322 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(230): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2686+93C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992322 | |||||||
chr15:39992601 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(230): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2687-168C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992601 | |||||||
chr15:39992648 | T | C | 3 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0005g0037 |
3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2687-121T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992648 | |||||||
chr15:39992919 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(240): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2766+71A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39992919 | |||||||
chr15:39993030 | G | GTCCA | 38 | a0001c0001t0001g0243 a0001c0001t0002g0119 a0001c0001t0002g0140 others(35): Show |
38 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2766+224_2766+227d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993030 | ||||||
chr15:39993030 | GTCCA | G | 14 | a0001c0001t0002g0177 a0001c0001t0003g0196 a0001c0001t0003g0197 others(11): Show |
14 | HG00673.hp2 HG01346.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2766+224_2766+227d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993030 | ||||||
chr15:39993048 | CCATCCAT others(21): Show |
C | 8 | a0001c0001t0001g0355 a0002c0002t0001g0286 a0002c0002t0001g0290 others(5): Show |
8 | HG01074.hp2 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.2766+228_2766+255d others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993048 | ||||||
chr15:39993052 | CCATCCAT others(17): Show |
C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0020 a0002c0002t0001g0022 others(7): Show |
11 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.2766+228_2766+251d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993052 | ||||||
chr15:39993056 | CCATCCAT others(13): Show |
C | 10 | a0002c0002t0001g0289 a0002c0002t0001g0293 a0002c0002t0001g0297 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2766+228_2766+247d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993056 | ||||||
chr15:39993064 | CCATCCAT others(5): Show |
C | 1 | a0002c0004t0001g0319 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2766+228_2766+239d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993064 | ||||||
chr15:39993091 | TCCATCCA others(9): Show |
T | 3 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0005g0037 |
3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2766+247_2766+262d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993091 | ||||||
chr15:39993103 | T | C | 60 | a0001c0001t0001g0204 a0001c0001t0002g0013 a0001c0001t0002g0111 others(57): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2766+255T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993103 | |||||||
chr15:39993138 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(240): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2766+290A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993138 | |||||||
chr15:39993149 | T | C | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2766+301T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993149 | |||||||
chr15:39993193 | C | T | 8 | a0002c0004t0001g0321 a0002c0004t0001g0322 a0007c0009t0003g0229 others(5): Show |
8 | HG01256.hp2 HG02300.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2766+345C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993193 | |||||||
chr15:39993194 | G | GTCCGTCC others(9): Show |
1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2766+350_2766+365d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993194 | ||||||
chr15:39993208 | C | T | 2 | a0003c0010t0001g0047 a0003c0010t0001g0048 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2766+360C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993208 | |||||||
chr15:39993227 | T | G | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0005g0037 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766+379T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993227 | |||||||
chr15:39993309 | T | A | 60 | a0001c0001t0001g0204 a0001c0001t0002g0013 a0001c0001t0002g0111 others(57): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2766+461T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993309 | |||||||
chr15:39993555 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2766+707C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993555 | |||||||
chr15:39993916 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(240): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2766+1068T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993916 | |||||||
chr15:39993967 | C | T | 1 | a0001c0005t0001g0132 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2766+1119C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993967 | |||||||
chr15:39994075 | C | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(239): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2766+1227C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994075 | |||||||
chr15:39994250 | T | G | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2766+1402T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994250 | |||||||
chr15:39994335 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(59): Show |
64 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2766+1487T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994335 | |||||||
chr15:39994425 | T | A | 7 | a0003c0010t0001g0047 a0003c0010t0001g0048 a0007c0009t0003g0229 others(4): Show |
7 | HG02451.hp2 NA18906.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.2766+1577T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994425 | |||||||
chr15:39994429 | G | A | 10 | a0002c0013t0001g0278 a0002c0013t0001g0279 a0002c0013t0001g0280 others(7): Show |
11 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2766+1581G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994429 | |||||||
chr15:39994482 | G | A | 2 | a0006c0012t0002g0176 a0017c0024t0002g0068 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2766+1634G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994482 | |||||||
chr15:39994540 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2766+1692T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994540 | |||||||
chr15:39994672 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(179): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2766+1824C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994672 | |||||||
chr15:39994731 | A | C | 1 | a0002c0002t0001g0290 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2766+1883A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994731 | |||||||
chr15:39994778 | T | G | 2 | a0001c0005t0001g0137 a0001c0005t0001g0152 |
2 | HG00609.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2766+1930T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994778 | |||||||
chr15:39994794 | G | A | 2 | a0002c0004t0001g0041 a0002c0004t0005g0114 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2766+1946G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994794 | |||||||
chr15:39994923 | C | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2767-2041C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994923 | |||||||
chr15:39995033 | G | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(198): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.2767-1931G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995033 | |||||||
chr15:39995166 | C | A | 1 | a0001c0005t0005g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2767-1798C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995166 | |||||||
chr15:39995308 | A | G | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2767-1656A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995308 | |||||||
chr15:39995321 | C | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2767-1643C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995321 | |||||||
chr15:39995436 | G | GC | 16 | a0002c0002t0007g0043 a0002c0004t0003g0039 a0002c0013t0001g0278 others(13): Show |
18 | HG00639.hp2 HG01169.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.2767-1524dupC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39995436 | ||||||
chr15:39995589 | G | A | 172 | a0001c0001t0001g0169 a0001c0001t0002g0009 a0001c0001t0002g0129 others(169): Show |
173 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2767-1375G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995589 | |||||||
chr15:39995781 | T | C | 28 | a0001c0001t0001g0355 a0002c0002t0001g0003 a0002c0002t0001g0020 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2767-1183T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995781 | |||||||
chr15:39995810 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0001c0005t0001g0246 others(16): Show |
19 | HG01081.hp1 HG01255.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2767-1154G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995810 | |||||||
chr15:39995821 | C | T | 1 | a0002c0002t0001g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2767-1143C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995821 | |||||||
chr15:39995830 | C | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2767-1134C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995830 | |||||||
chr15:39995872 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(212): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.2767-1092G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995872 | |||||||
chr15:39995985 | C | T | 1 | a0002c0004t0002g0316 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2767-979C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995985 | |||||||
chr15:39996020 | G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2767-944G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996020 | |||||||
chr15:39996429 | G | A | 2 | a0002c0002t0002g0336 a0002c0002t0002g0337 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2767-535G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996429 | |||||||
chr15:39996508 | C | A | 2 | a0003c0010t0001g0047 a0003c0010t0001g0048 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2767-456C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996508 | |||||||
chr15:39996601 | C | A | 1 | a0007c0009t0003g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2767-363C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996601 | |||||||
chr15:39997105 | C | T | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2868+40C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997105 | |||||||
chr15:39997362 | A | G | 1 | a0014c0035t0003g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2868+297A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997362 | |||||||
chr15:39997381 | T | C | 1 | a0003c0003t0002g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2868+316T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997381 | |||||||
chr15:39997386 | C | A | 1 | a0002c0002t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2868+321C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997386 | |||||||
chr15:39997387 | T | C | 5 | a0007c0009t0003g0229 a0007c0009t0003g0231 a0007c0009t0003g0233 others(2): Show |
5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2868+322T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997387 | |||||||
chr15:39997407 | C | G | 3 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0005g0037 |
3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2868+342C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997407 | |||||||
chr15:39997434 | C | A | 1 | a0003c0003t0001g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2868+369C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997434 | |||||||
chr15:39997629 | G | A | 3 | a0004c0006t0006g0251 a0004c0006t0006g0252 a0004c0006t0006g0260 |
3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2868+564G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997629 | |||||||
chr15:39997670 | G | A | 5 | a0002c0002t0007g0043 a0002c0004t0003g0039 a0003c0026t0001g0011 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2868+605G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997670 | |||||||
chr15:39997670 | G | C | 1 | a0002c0002t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2868+605G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997670 | |||||||
chr15:39997763 | A | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2868+698A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997763 | |||||||
chr15:39997826 | A | T | 27 | a0001c0001t0001g0355 a0002c0002t0001g0003 a0002c0002t0001g0020 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2868+761A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997826 | |||||||
chr15:39997962 | T | A | 1 | a0002c0004t0002g0353 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2869-769T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997962 | |||||||
chr15:39998084 | G | C | 1 | a0001c0001t0003g0208 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2869-647G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998084 | |||||||
chr15:39998135 | T | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2869-596T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998135 | |||||||
chr15:39998215 | A | AT | 11 | a0002c0013t0001g0278 a0002c0013t0001g0279 a0002c0013t0001g0280 others(8): Show |
13 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2869-508dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998215 | ||||||
chr15:39998257 | GT | G | 6 | a0002c0002t0002g0241 a0002c0002t0002g0242 a0003c0003t0001g0058 others(3): Show |
6 | HG02145.hp1 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2869-462delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998257 | ||||||
chr15:39998265 | T | G | 5 | a0001c0001t0003g0217 a0002c0011t0002g0096 a0002c0011t0002g0301 others(2): Show |
5 | NA18953.hp2 NA18995.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.2869-466T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998265 | |||||||
chr15:39998266 | T | G | 3 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0004g0236 |
3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2869-465T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998266 | |||||||
chr15:39998269 | T | G | 5 | a0001c0005t0001g0125 a0001c0005t0005g0123 a0001c0005t0005g0124 others(2): Show |
5 | HG01169.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2869-462T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998269 | |||||||
chr15:39998269 | T | TTG | 7 | a0002c0004t0001g0041 a0002c0004t0001g0357 a0002c0004t0001g0358 others(4): Show |
7 | HG00642.hp1 HG02723.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.2869-462_2869-461i others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998269 | |||||||
chr15:39998270 | G | GT | 83 | a0001c0001t0002g0009 a0001c0005t0001g0134 a0001c0005t0001g0135 others(80): Show |
86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.2869-457dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998270 | ||||||
chr15:39998270 | G | T | 16 | a0001c0001t0002g0158 a0001c0005t0001g0125 a0001c0005t0005g0123 others(13): Show |
16 | HG00597.hp1 HG00642.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.2869-461G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998270 | |||||||
chr15:39998275 | G | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(264): Show |
272 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.2869-456G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998275 | |||||||
chr15:39998280 | T | G | 32 | a0001c0001t0001g0355 a0001c0001t0003g0185 a0001c0001t0003g0186 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.2869-451T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998280 | |||||||
chr15:39998299 | G | T | 1 | a0002c0004t0001g0349 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2869-432G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998299 | |||||||
chr15:39998460 | CA | C | 9 | a0001c0001t0003g0109 a0001c0001t0003g0110 a0001c0001t0003g0174 others(6): Show |
9 | HG02015.hp1 HG02040.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2869-269delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998460 | ||||||
chr15:39998505 | G | A | 84 | a0001c0005t0001g0125 a0001c0005t0001g0134 a0001c0005t0001g0135 others(81): Show |
85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2869-226G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998505 | |||||||
chr15:39998519 | A | G | 1 | a0001c0001t0003g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2869-212A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998519 | |||||||
chr15:39998929 | C | G | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2922+145C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39998929 | |||||||
chr15:39999020 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2922+236G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999020 | |||||||
chr15:39999024 | T | C | 1 | a0001c0001t0003g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2922+240T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999024 | |||||||
chr15:39999047 | C | G | 3 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0004g0236 |
3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2922+263C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999047 | |||||||
chr15:39999078 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(75): Show |
80 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2922+294T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999078 | |||||||
chr15:39999242 | A | T | 356 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(353): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2922+458A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999242 | |||||||
chr15:39999602 | A | G | 1 | a0004c0006t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2922+818A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999602 | |||||||
chr15:39999666 | T | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(62): Show |
67 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.2922+882T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999666 | |||||||
chr15:39999889 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(75): Show |
80 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2923-1099A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999889 | |||||||
chr15:39999916 | C | T | 1 | a0014c0035t0003g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2923-1072C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999916 | |||||||
chr15:40000057 | A | G | 84 | a0001c0005t0001g0125 a0001c0005t0001g0134 a0001c0005t0001g0135 others(81): Show |
85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2923-931A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000057 | |||||||
chr15:40000185 | A | G | 4 | a0001c0005t0005g0108 a0002c0004t0005g0237 a0010c0018t0005g0238 others(1): Show |
4 | HG01496.hp2 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2923-803A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000185 | |||||||
chr15:40000364 | C | G | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2923-624C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000364 | |||||||
chr15:40000755 | G | C | 1 | a0005c0008t0004g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2923-233G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000755 | |||||||
chr15:40000821 | T | C | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923-167T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000821 | |||||||
chr15:40000835 | AAAT | A | 83 | a0001c0005t0001g0125 a0001c0005t0001g0134 a0001c0005t0001g0135 others(80): Show |
84 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2923-149_2923-147d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 40000835 | ||||||
chr15:40000926 | C | T | 2 | a0001c0001t0002g0120 a0003c0003t0002g0066 |
2 | HG01099.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2923-62C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000926 | |||||||
chr15:40000954 | A | T | 1 | a0006c0012t0003g0269 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2923-34A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000954 | |||||||
chr15:40000975 | G | C | 3 | a0001c0001t0001g0167 a0001c0001t0011g0163 a0006c0012t0001g0267 |
3 | NA18948.hp2 NA18956.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.2923-13G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000975 | |||||||
chr15:40001236 | C | A | 8 | a0003c0003t0002g0056 a0003c0003t0002g0078 a0003c0003t0002g0080 others(5): Show |
8 | NA18612.hp2 NA18962.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.3159+12C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001236 | |||||||
chr15:40001329 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(52): Show |
57 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3159+105T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001329 | |||||||
chr15:40001486 | C | T | 2 | a0002c0002t0003g0050 a0002c0002t0003g0276 |
2 | HG00642.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3159+262C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001486 | |||||||
chr15:40001523 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3159+299G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001523 | |||||||
chr15:40001552 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3159+328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001552 | |||||||
chr15:40001633 | C | CA | 244 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0001c0001t0002g0009 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.3159+427dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr15 | 40001633 | ||||||
chr15:40001633 | C | CAA | 27 | a0001c0001t0001g0243 a0001c0001t0002g0158 a0001c0001t0003g0245 others(24): Show |
29 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.3159+426_3159+427d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr15 | 40001633 | ||||||
chr15:40001685 | A | T | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3159+461A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001685 | |||||||
chr15:40001688 | C | T | 2 | a0003c0003t0002g0098 a0003c0003t0002g0102 |
2 | HG01346.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.3159+464C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001688 | |||||||
chr15:40001807 | C | G | 1 | a0008c0015t0006g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3159+583C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001807 | |||||||
chr15:40001864 | A | C | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3159+640A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001864 | |||||||
chr15:40001983 | T | C | 1 | a0004c0007t0003g0258 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3160-730T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001983 | |||||||
chr15:40001992 | G | A | 76 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(73): Show |
76 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.3160-721G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001992 | |||||||
chr15:40002253 | C | G | 1 | a0002c0002t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3160-460C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002253 | |||||||
chr15:40002385 | C | T | 11 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(8): Show |
11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3160-328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002385 | |||||||
chr15:40002387 | C | T | 1 | a0002c0002t0001g0293 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3160-326C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002387 | |||||||
chr15:40002577 | G | C | 1 | a0001c0001t0002g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3160-136G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002577 | |||||||
chr15:40002590 | C | G | 1 | a0002c0004t0001g0319 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3160-123C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002590 | |||||||
chr15:40002705 | T | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.3160-8T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002705 | |||||||
chr15:40003551 | T | C | 2 | a0005c0008t0001g0296 a0005c0008t0001g0356 |
2 | HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3357+237T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003551 | |||||||
chr15:40003663 | G | A | 1 | a0002c0030t0002g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3357+349G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003663 | |||||||
chr15:40003758 | C | T | 235 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.3357+444C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003758 | |||||||
chr15:40003794 | G | A | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3357+480G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003794 | |||||||
chr15:40004046 | T | C | 12 | a0001c0001t0002g0111 a0001c0001t0002g0205 a0001c0001t0003g0109 others(9): Show |
12 | HG00621.hp1 HG02015.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.3357+732T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004046 | |||||||
chr15:40004128 | G | A | 274 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(271): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.3357+814G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004128 | |||||||
chr15:40004140 | A | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3357+826A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004140 | |||||||
chr15:40004226 | C | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3357+912C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004226 | |||||||
chr15:40004249 | A | C | 23 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0001c0001t0004g0244 others(20): Show |
25 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.3357+935A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004249 | |||||||
chr15:40004354 | CTGTT | C | 3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1042_3357+104 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40004354 | ||||||
chr15:40004487 | G | A | 1 | a0002c0002t0002g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3357+1173G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004487 | |||||||
chr15:40004497 | C | T | 11 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(8): Show |
11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3357+1183C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004497 | |||||||
chr15:40004498 | C | T | 138 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(135): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.3357+1184C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004498 | |||||||
chr15:40004721 | T | A | 23 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0001c0001t0004g0244 others(20): Show |
25 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.3357+1407T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004721 | |||||||
chr15:40004727 | T | A | 28 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3357+1413T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004727 | |||||||
chr15:40004727 | T | C | 3 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0003c0003t0001g0343 |
3 | HG02055.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3357+1413T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004727 | |||||||
chr15:40004814 | C | G | 3 | a0002c0002t0007g0043 a0009c0016t0007g0042 a0009c0016t0007g0044 |
3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3357+1500C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004814 | |||||||
chr15:40004845 | C | T | 8 | a0002c0002t0007g0043 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3357+1531C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004845 | |||||||
chr15:40004851 | C | T | 3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1537C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004851 | |||||||
chr15:40004852 | A | G | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.3357+1538A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004852 | |||||||
chr15:40004873 | A | G | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3357+1559A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004873 | |||||||
chr15:40004898 | T | A | 8 | a0002c0002t0007g0043 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3357+1584T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004898 | |||||||
chr15:40005018 | T | A | 31 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.3357+1704T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005018 | |||||||
chr15:40005046 | T | A | 1 | a0001c0001t0003g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3357+1732T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005046 | |||||||
chr15:40005067 | A | G | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3357+1753A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005067 | |||||||
chr15:40005093 | T | G | 12 | a0001c0001t0004g0244 a0002c0013t0001g0278 a0002c0013t0001g0279 others(9): Show |
14 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3357+1779T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005093 | |||||||
chr15:40005140 | A | G | 3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1826A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005140 | |||||||
chr15:40005193 | T | C | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1823T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005193 | |||||||
chr15:40005261 | A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3358-1755A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005261 | |||||||
chr15:40005306 | T | A | 84 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0125 others(81): Show |
85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.3358-1710T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005306 | |||||||
chr15:40005456 | C | T | 1 | a0013c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3358-1560C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005456 | |||||||
chr15:40005516 | C | CA | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1493dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40005516 | ||||||
chr15:40005531 | C | T | 4 | a0002c0002t0007g0043 a0003c0026t0001g0011 a0009c0016t0007g0042 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1485C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005531 | |||||||
chr15:40005551 | G | A | 4 | a0002c0002t0007g0043 a0003c0026t0001g0011 a0009c0016t0007g0042 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1465G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005551 | |||||||
chr15:40005565 | A | G | 8 | a0002c0002t0007g0043 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3358-1451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005565 | |||||||
chr15:40005707 | G | A | 1 | a0004c0007t0002g0266 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3358-1309G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005707 | |||||||
chr15:40005759 | G | A | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.3358-1257G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005759 | |||||||
chr15:40005867 | G | A | 11 | a0002c0013t0001g0278 a0002c0013t0001g0279 a0002c0013t0001g0280 others(8): Show |
13 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3358-1149G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005867 | |||||||
chr15:40005939 | C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3358-1077C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005939 | |||||||
chr15:40006157 | C | T | 85 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0125 others(82): Show |
86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3358-859C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006157 | |||||||
chr15:40006492 | G | A | 8 | a0002c0002t0007g0043 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3358-524G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006492 | |||||||
chr15:40006669 | T | A | 139 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(136): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3358-347T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006669 | |||||||
chr15:40006670 | T | A | 238 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.3358-346T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006670 | |||||||
chr15:40006711 | A | T | 1 | a0002c0011t0002g0331 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3358-305A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006711 | |||||||
chr15:40006815 | C | T | 77 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(74): Show |
77 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.3358-201C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006815 | |||||||
chr15:40006999 | TTTTG | T | 8 | a0005c0008t0001g0296 a0005c0008t0001g0298 a0005c0008t0001g0356 others(5): Show |
10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3358-13_3358-10del others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40006999 | ||||||
chr15:40007299 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3407+234A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007299 | |||||||
chr15:40007427 | G | A | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3407+362G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007427 | |||||||
chr15:40007486 | A | G | 1 | a0002c0002t0001g0359 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3407+421A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007486 | |||||||
chr15:40007713 | T | C | 8 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0004g0015 others(5): Show |
8 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3408-314T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007713 | |||||||
chr15:40007802 | A | T | 4 | a0003c0003t0002g0008 a0003c0003t0002g0055 a0003c0003t0002g0072 others(1): Show |
4 | NA18940.hp1 NA18969.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3408-225A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007802 | |||||||
chr15:40007854 | A | G | 8 | a0002c0002t0007g0043 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3408-173A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007854 | |||||||
chr15:40007891 | T | C | 237 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.3408-136T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007891 | |||||||
chr15:40007920 | C | T | 11 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(8): Show |
11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3408-107C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007920 | |||||||
chr15:40007973 | A | T | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3408-54A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007973 | |||||||
chr15:40008013 | G | C | 111 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0001c0001t0002g0009 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.3408-14G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40008013 | |||||||
chr15:40008242 | T | G | 89 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0125 others(86): Show |
90 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.3576+47T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008242 | |||||||
chr15:40008346 | T | C | 12 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3576+151T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008346 | |||||||
chr15:40008443 | T | C | 1 | a0002c0004t0002g0348 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3576+248T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008443 | |||||||
chr15:40008490 | G | T | 21 | a0001c0001t0003g0245 a0001c0001t0004g0244 a0002c0002t0001g0359 others(18): Show |
23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.3576+295G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008490 | |||||||
chr15:40008617 | A | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0130 others(61): Show |
67 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3576+422A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008617 | |||||||
chr15:40008857 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0003g0113 |
2 | HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.3576+662A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008857 | |||||||
chr15:40008862 | G | A | 12 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3576+667G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008862 | |||||||
chr15:40008899 | A | G | 4 | a0001c0005t0001g0246 a0002c0031t0009g0045 a0003c0010t0001g0047 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3576+704A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008899 | |||||||
chr15:40008969 | G | A | 273 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.3577-645G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008969 | |||||||
chr15:40008996 | T | C | 5 | a0002c0002t0004g0015 a0002c0002t0004g0016 a0002c0002t0004g0017 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3577-618T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008996 | |||||||
chr15:40009069 | T | TTTTTG | 93 | a0001c0001t0002g0222 a0001c0005t0001g0032 a0001c0005t0001g0034 others(90): Show |
94 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.3577-509_3577-505d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009069 | T | TTTTTGTT others(3): Show |
47 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(44): Show |
47 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.3577-514_3577-505d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009069 | T | TTTTTGTT others(8): Show |
5 | a0001c0005t0005g0153 a0002c0004t0004g0330 a0004c0007t0001g0250 others(2): Show |
5 | HG00741.hp1 HG01978.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3577-519_3577-505d others(17): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009069 | TTTTTG | T | 53 | a0001c0001t0001g0206 a0001c0001t0001g0243 a0001c0001t0001g0355 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.3577-509_3577-505d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009069 | TTTTTGTT others(3): Show |
T | 4 | a0001c0005t0001g0246 a0002c0004t0001g0327 a0003c0010t0001g0047 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3577-514_3577-505d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009069 | TTTTTGTT others(8): Show |
T | 1 | a0005c0014t0004g0294 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3577-519_3577-505d others(17): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | ||||||
chr15:40009170 | G | A | 12 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3577-444G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40009170 | |||||||
chr15:40009301 | C | A | 79 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(76): Show |
79 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.3577-313C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40009301 | |||||||
chr15:40010042 | C | T | 204 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(201): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.3693+312C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010042 | |||||||
chr15:40010224 | G | A | 18 | a0001c0001t0003g0245 a0001c0001t0004g0244 a0002c0002t0001g0359 others(15): Show |
20 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3693+494G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010224 | |||||||
chr15:40010240 | G | A | 204 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(201): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.3693+510G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010240 | |||||||
chr15:40010346 | C | T | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3693+616C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010346 | |||||||
chr15:40010461 | T | C | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3693+731T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010461 | |||||||
chr15:40010486 | G | A | 18 | a0001c0001t0002g0138 a0002c0002t0001g0035 a0002c0002t0002g0040 others(15): Show |
18 | HG02145.hp1 HG02258.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.3693+756G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010486 | |||||||
chr15:40010572 | G | C | 2 | a0002c0002t0002g0313 a0002c0002t0010g0046 |
2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3694-709G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010572 | |||||||
chr15:40010629 | G | GA | 273 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.3694-650dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40010629 | ||||||
chr15:40010646 | CAG | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0219 others(4): Show |
7 | HG00597.hp1 HG03669.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.3694-632_3694-631d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40010646 | ||||||
chr15:40010769 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3694-512G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010769 | |||||||
chr15:40010772 | C | G | 85 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0125 others(82): Show |
86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3694-509C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010772 | |||||||
chr15:40010799 | G | C | 1 | a0002c0004t0001g0347 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3694-482G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010799 | |||||||
chr15:40010830 | A | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3694-451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010830 | |||||||
chr15:40011092 | ATAAGT | A | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0005g0037 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3694-185_3694-181d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40011092 | ||||||
chr15:40011105 | G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3694-176G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40011105 | |||||||
chr15:40011382 | C | G | 1 | a0005c0014t0004g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3759+36C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011382 | |||||||
chr15:40011641 | G | A | 190 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(187): Show |
193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.3759+295G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011641 | |||||||
chr15:40011969 | T | G | 237 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.3759+623T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011969 | |||||||
chr15:40012047 | C | A | 2 | a0001c0001t0002g0009 a0002c0002t0002g0333 |
2 | HG00597.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.3759+701C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012047 | |||||||
chr15:40012093 | T | G | 1 | a0002c0004t0002g0314 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3759+747T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012093 | |||||||
chr15:40012206 | A | C | 102 | a0001c0001t0001g0243 a0001c0005t0001g0032 a0001c0005t0001g0034 others(99): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.3759+860A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012206 | |||||||
chr15:40012512 | T | C | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3759+1166T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012512 | |||||||
chr15:40012639 | A | G | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3759+1293A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012639 | |||||||
chr15:40012662 | CT | C | 9 | a0001c0001t0001g0243 a0001c0001t0002g0119 a0001c0001t0003g0189 others(6): Show |
9 | HG01168.hp1 HG02015.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3759+1329delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr15 | 40012662 | ||||||
chr15:40012701 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3759+1355G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012701 | |||||||
chr15:40012849 | G | A | 1 | a0002c0004t0001g0300 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3759+1503G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012849 | |||||||
chr15:40012875 | T | C | 1 | a0005c0014t0004g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3759+1529T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012875 | |||||||
chr15:40012929 | G | T | 3 | a0002c0004t0001g0303 a0002c0004t0001g0312 a0002c0004t0014g0302 |
3 | NA18951.hp2 NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3759+1583G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012929 | |||||||
chr15:40012961 | C | T | 80 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(77): Show |
80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3759+1615C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012961 | |||||||
chr15:40013264 | G | A | 1 | a0004c0007t0001g0250 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3759+1918G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013264 | |||||||
chr15:40013322 | G | A | 1 | a0011c0017t0003g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3759+1976G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013322 | |||||||
chr15:40013414 | C | T | 80 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(77): Show |
80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3759+2068C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013414 | |||||||
chr15:40013422 | G | A | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3759+2076G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013422 | |||||||
chr15:40013517 | C | T | 6 | a0001c0001t0003g0245 a0002c0002t0001g0359 a0002c0002t0001g0361 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3759+2171C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013517 | |||||||
chr15:40013985 | A | C | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3760-2517A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013985 | |||||||
chr15:40014063 | T | A | 80 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(77): Show |
80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3760-2439T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014063 | |||||||
chr15:40014117 | C | T | 1 | a0005c0008t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3760-2385C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014117 | |||||||
chr15:40014123 | C | T | 5 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3760-2379C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014123 | |||||||
chr15:40014133 | C | A | 95 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0129 others(92): Show |
97 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.3760-2369C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014133 | |||||||
chr15:40014308 | G | T | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3760-2194G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014308 | |||||||
chr15:40014347 | C | T | 3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3760-2155C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014347 | |||||||
chr15:40014420 | G | A | 1 | a0002c0002t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3760-2082G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014420 | |||||||
chr15:40014737 | C | T | 1 | a0002c0013t0001g0278 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3760-1765C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014737 | |||||||
chr15:40014894 | A | C | 259 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.3760-1608A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014894 | |||||||
chr15:40014979 | T | C | 1 | a0001c0001t0003g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3760-1523T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014979 | |||||||
chr15:40015273 | G | A | 2 | a0004c0006t0001g0259 a0004c0037t0001g0273 |
2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3760-1229G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015273 | |||||||
chr15:40015518 | G | A | 3 | a0001c0001t0001g0169 a0004c0006t0001g0254 a0004c0006t0001g0255 |
3 | HG02129.hp1 HG02698.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3760-984G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015518 | |||||||
chr15:40015574 | A | G | 206 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(203): Show |
209 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.3760-928A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015574 | |||||||
chr15:40015612 | A | G | 5 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3760-890A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015612 | |||||||
chr15:40015706 | T | C | 1 | a0002c0002t0005g0292 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3760-796T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015706 | |||||||
chr15:40015960 | A | C | 11 | a0002c0013t0001g0278 a0002c0013t0001g0279 a0002c0013t0001g0280 others(8): Show |
13 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3760-542A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015960 | |||||||
chr15:40016100 | G | A | 7 | a0001c0001t0001g0204 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.3760-402G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016100 | |||||||
chr15:40016159 | A | T | 1 | a0001c0001t0003g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3760-343A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016159 | |||||||
chr15:40016397 | C | T | 2 | a0001c0005t0001g0032 a0001c0005t0001g0034 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3760-105C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016397 | |||||||
chr15:40016447 | A | C | 8 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0004g0015 others(5): Show |
8 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3760-55A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016447 | |||||||
chr15:40016836 | A | G | 2 | a0001c0001t0003g0245 a0003c0003t0001g0058 |
2 | HG01081.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3930+164A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/38 | chr15 | 40016836 | |||||||
chr15:40017001 | A | G | 1 | a0002c0004t0001g0274 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3931-107A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/38 | chr15 | 40017001 | |||||||
chr15:40017281 | T | A | 1 | a0003c0003t0013g0086 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4065+39T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017281 | |||||||
chr15:40017363 | T | C | 1 | a0001c0005t0005g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4065+121T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017363 | |||||||
chr15:40017370 | A | G | 1 | a0013c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4065+128A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017370 | |||||||
chr15:40017495 | C | G | 1 | a0001c0001t0002g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4065+253C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017495 | |||||||
chr15:40017501 | C | CATATATA others(4): Show |
1 | a0004c0006t0004g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4065+259_4065+260i others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017501 | |||||||
chr15:40017501 | C | CTATATAT others(1): Show |
4 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(1): Show |
4 | NA18972.hp2 NA19074.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+305_4065+312d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(3): Show |
4 | a0001c0001t0003g0190 a0001c0001t0003g0197 a0001c0001t0003g0224 others(1): Show |
4 | HG02738.hp2 NA19007.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+303_4065+312d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(5): Show |
1 | a0001c0001t0005g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4065+301_4065+312d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(7): Show |
6 | a0001c0001t0003g0012 a0001c0001t0003g0171 a0001c0001t0003g0188 others(3): Show |
6 | HG00438.hp1 HG01168.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+299_4065+312d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(9): Show |
6 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0196 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+297_4065+312d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(11): Show |
3 | a0001c0001t0003g0110 a0001c0001t0003g0221 a0002c0002t0003g0049 |
3 | HG03471.hp2 NA19054.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4065+295_4065+312d others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(13): Show |
6 | a0001c0001t0003g0109 a0001c0001t0003g0179 a0001c0001t0003g0187 others(3): Show |
6 | HG02132.hp2 HG03486.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+293_4065+312d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(15): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0154 a0001c0001t0003g0178 others(1): Show |
4 | HG02027.hp1 HG02145.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+291_4065+312d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(17): Show |
1 | a0001c0001t0003g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4065+289_4065+312d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(19): Show |
2 | a0001c0001t0003g0172 a0001c0001t0003g0201 |
2 | HG02155.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.4065+287_4065+312d others(28): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(23): Show |
1 | a0002c0002t0003g0276 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4065+283_4065+312d others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTATATAT others(27): Show |
3 | a0001c0001t0002g0126 a0001c0001t0003g0170 a0001c0001t0003g0181 |
3 | HG02165.hp1 HG02602.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.4065+279_4065+312d others(36): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTATATA others(6): Show |
1 | a0003c0003t0013g0086 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(15): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTTATAT others(3): Show |
2 | a0002c0002t0001g0361 a0002c0002t0004g0236 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4065+260_4065+261i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTTATAT others(7): Show |
1 | a0002c0002t0001g0359 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4065+260_4065+261i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTTATAT others(9): Show |
2 | a0003c0003t0002g0065 a0003c0025t0004g0010 |
2 | HG01978.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4065+260_4065+261i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTTTTAT others(3): Show |
1 | a0009c0016t0007g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | C | CTTTTTAT others(5): Show |
1 | a0002c0002t0007g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATA | C | 12 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0013 others(9): Show |
12 | HG00597.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4065+307_4065+312d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(1): Show |
C | 5 | a0001c0001t0002g0009 a0002c0002t0002g0242 a0004c0006t0003g0344 others(2): Show |
5 | HG02965.hp1 HG03490.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+305_4065+312d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(3): Show |
C | 5 | a0001c0001t0001g0243 a0001c0001t0003g0207 a0001c0001t0003g0226 others(2): Show |
5 | HG02818.hp2 HG02895.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+303_4065+312d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(5): Show |
C | 2 | a0003c0003t0002g0055 a0003c0003t0002g0076 |
2 | NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4065+301_4065+312d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(7): Show |
C | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0005t0001g0180 others(2): Show |
5 | HG02602.hp1 NA18948.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+299_4065+312d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(9): Show |
C | 6 | a0001c0001t0005g0023 a0001c0001t0005g0029 a0001c0001t0005g0031 others(3): Show |
6 | HG00621.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+297_4065+312d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(11): Show |
C | 19 | a0001c0001t0002g0128 a0001c0005t0001g0125 a0001c0005t0005g0108 others(16): Show |
19 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.4065+295_4065+312d others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(13): Show |
C | 83 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(80): Show |
84 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.4065+293_4065+312d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(15): Show |
C | 2 | a0001c0001t0003g0184 a0011c0017t0003g0341 |
2 | HG02523.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4065+291_4065+312d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(17): Show |
C | 6 | a0001c0001t0003g0175 a0001c0005t0001g0246 a0002c0031t0009g0045 others(3): Show |
6 | HG00140.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+289_4065+312d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(21): Show |
C | 1 | a0001c0001t0001g0165 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4065+285_4065+312d others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017501 | CTATATAT others(23): Show |
C | 8 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 others(5): Show |
8 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4065+283_4065+312d others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | ||||||
chr15:40017502 | TATATATA others(12): Show |
T | 1 | a0004c0007t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4065+261_4065+279d others(21): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017502 | |||||||
chr15:40017503 | A | T | 76 | a0001c0001t0002g0129 a0001c0001t0002g0138 a0001c0001t0002g0147 others(73): Show |
78 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.4065+261A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017503 | |||||||
chr15:40017509 | A | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0219 a0001c0001t0002g0222 others(3): Show |
6 | HG00597.hp1 HG03927.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.4065+267A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017509 | |||||||
chr15:40017511 | A | T | 4 | a0001c0001t0002g0009 a0002c0002t0002g0242 a0006c0012t0002g0176 others(1): Show |
4 | HG02965.hp1 HG03669.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+269A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017511 | |||||||
chr15:40017513 | A | T | 2 | a0001c0001t0001g0243 a0003c0003t0002g0072 |
2 | HG02895.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4065+271A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017513 | |||||||
chr15:40017515 | A | T | 2 | a0003c0003t0002g0055 a0003c0003t0002g0076 |
2 | NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4065+273A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017515 | |||||||
chr15:40017517 | A | T | 2 | a0001c0005t0001g0180 a0001c0020t0001g0173 |
2 | NA18974.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.4065+275A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017517 | |||||||
chr15:40017519 | A | T | 3 | a0002c0002t0010g0046 a0003c0010t0001g0079 a0004c0007t0001g0215 |
3 | HG00621.hp2 HG02572.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.4065+277A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017519 | |||||||
chr15:40017521 | A | T | 17 | a0001c0005t0001g0125 a0001c0005t0005g0108 a0001c0005t0005g0123 others(14): Show |
17 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.4065+279A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017521 | |||||||
chr15:40017522 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0001 | 3 | NA18962.hp1 NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4065+303_4065+304i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017522 | ||||||
chr15:40017523 | A | T | 69 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0132 others(66): Show |
70 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.4065+281A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017523 | |||||||
chr15:40017527 | A | T | 3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 |
3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4065+285A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017527 | |||||||
chr15:40017533 | A | T | 5 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+291A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017533 | |||||||
chr15:40017543 | A | G | 16 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(13): Show |
16 | HG00438.hp2 HG00673.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.4065+301A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017543 | |||||||
chr15:40017545 | A | G | 14 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0219 others(11): Show |
14 | HG00597.hp1 HG01975.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4065+303A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017545 | |||||||
chr15:40017547 | A | ATATGTAT others(1): Show |
3 | a0001c0001t0002g0142 a0003c0003t0001g0106 a0005c0008t0004g0004 |
4 | HG02165.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+308_4065+309i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017547 | ||||||
chr15:40017547 | A | G | 20 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(17): Show |
21 | HG00438.hp2 HG00673.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.4065+305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017547 | |||||||
chr15:40017548 | T | C | 99 | a0001c0001t0001g0243 a0001c0005t0001g0032 a0001c0005t0001g0034 others(96): Show |
100 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.4065+306T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017548 | |||||||
chr15:40017551 | A | ATATATAC others(3): Show |
1 | a0002c0002t0004g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(7): Show |
2 | a0003c0003t0003g0091 a0007c0009t0003g0231 |
2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(9): Show |
3 | a0002c0002t0004g0016 a0007c0009t0003g0233 a0015c0023t0003g0232 |
3 | HG03579.hp2 NA18974.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(15): Show |
1 | a0007c0009t0003g0234 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(17): Show |
1 | a0007c0009t0003g0229 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(23): Show |
1 | a0003c0003t0002g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(21): Show |
2 | a0003c0003t0002g0082 a0011c0017t0002g0239 |
2 | HG02145.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0127 a0002c0002t0001g0299 |
2 | HG03654.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(19): Show |
8 | a0002c0002t0002g0308 a0003c0003t0002g0083 a0003c0003t0002g0084 others(5): Show |
8 | HG01346.hp2 HG03139.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(28): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(21): Show |
1 | a0008c0015t0005g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0002c0002t0001g0297 others(2): Show |
5 | HG00280.hp2 HG02056.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(17): Show |
2 | a0003c0003t0002g0075 a0003c0003t0002g0095 |
2 | NA18949.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(9): Show |
3 | a0001c0001t0011g0163 a0002c0019t0001g0284 a0004c0037t0001g0273 |
3 | HG01106.hp2 HG01175.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(15): Show |
3 | a0003c0003t0002g0059 a0003c0003t0002g0070 a0003c0003t0002g0081 |
3 | NA18979.hp2 NA19030.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0206 a0002c0002t0001g0287 a0002c0002t0001g0290 |
3 | HG01361.hp1 HG03927.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(13): Show |
7 | a0002c0002t0002g0241 a0002c0002t0002g0309 a0003c0003t0002g0054 others(4): Show |
7 | HG02273.hp2 HG03704.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(5): Show |
5 | a0001c0001t0001g0130 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG02004.hp1 HG02074.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(11): Show |
10 | a0002c0002t0002g0310 a0003c0003t0001g0067 a0003c0003t0001g0099 others(7): Show |
10 | HG02027.hp2 HG02071.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(13): Show |
3 | a0002c0002t0001g0159 a0005c0008t0001g0298 a0005c0008t0004g0339 |
3 | HG02074.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(3): Show |
4 | a0002c0002t0001g0003 a0002c0002t0001g0288 a0002c0002t0001g0360 others(1): Show |
5 | HG00639.hp1 HG01069.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(9): Show |
9 | a0001c0001t0002g0129 a0001c0001t0002g0147 a0002c0002t0001g0035 others(6): Show |
9 | HG00408.hp1 HG00408.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0144 a0002c0002t0001g0162 |
2 | NA18991.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(1): Show |
3 | a0002c0002t0001g0022 a0002c0002t0001g0286 a0004c0006t0004g0248 |
3 | HG01074.hp2 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(7): Show |
2 | a0003c0003t0002g0008 a0004c0006t0002g0253 |
2 | HG04184.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATAT others(9): Show |
3 | a0002c0002t0001g0160 a0003c0003t0006g0105 a0004c0006t0006g0251 |
3 | HG00673.hp1 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATG | 4 | a0001c0001t0001g0164 a0002c0002t0001g0270 a0004c0006t0001g0210 others(1): Show |
4 | HG00140.hp2 HG00609.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATGT others(5): Show |
7 | a0001c0001t0002g0138 a0002c0002t0002g0336 a0002c0002t0002g0337 others(4): Show |
7 | HG01123.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0133 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATGT others(7): Show |
5 | a0001c0001t0002g0143 a0001c0001t0012g0155 a0002c0019t0001g0281 others(2): Show |
5 | HG01099.hp1 HG01169.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATATGT others(11): Show |
1 | a0002c0002t0002g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATGTAT others(3): Show |
3 | a0003c0003t0002g0061 a0003c0003t0002g0066 a0003c0003t0003g0060 |
3 | HG01099.hp2 HG01109.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.4065+316_4065+317i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATATGTAT others(5): Show |
3 | a0001c0001t0002g0141 a0004c0006t0006g0252 a0005c0008t0001g0296 |
3 | HG01516.hp2 HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.4065+316_4065+317i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATGTATAT others(1): Show |
10 | a0002c0002t0002g0040 a0002c0002t0002g0313 a0002c0002t0002g0350 others(7): Show |
10 | HG01255.hp1 HG01496.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.4065+310_4065+311i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | ATGTATGT others(3): Show |
2 | a0001c0001t0002g0156 a0008c0015t0006g0027 |
2 | HG02135.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4065+310_4065+311i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | ||||||
chr15:40017551 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(160): Show |
168 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.4065+309A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017551 | |||||||
chr15:40017655 | C | G | 3 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0004g0236 |
3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4065+413C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017655 | |||||||
chr15:40017670 | C | T | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4065+428C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017670 | |||||||
chr15:40017683 | C | T | 1 | a0004c0006t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4065+441C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017683 | |||||||
chr15:40017775 | G | A | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4065+533G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017775 | |||||||
chr15:40017821 | A | T | 1 | a0002c0004t0001g0326 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4065+579A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017821 | |||||||
chr15:40017953 | A | G | 1 | a0002c0004t0001g0342 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4065+711A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017953 | |||||||
chr15:40018030 | G | T | 8 | a0001c0005t0001g0246 a0002c0004t0003g0036 a0002c0004t0003g0038 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4065+788G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018030 | |||||||
chr15:40018334 | C | T | 15 | a0001c0005t0001g0125 a0001c0005t0001g0134 a0001c0005t0001g0135 others(12): Show |
15 | HG00280.hp1 HG00741.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.4066-759C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018334 | |||||||
chr15:40018392 | A | G | 1 | a0002c0002t0010g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4066-701A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018392 | |||||||
chr15:40018442 | AT | A | 21 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0001c0001t0004g0244 others(18): Show |
23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4066-641delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40018442 | ||||||
chr15:40018600 | G | A | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4066-493G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018600 | |||||||
chr15:40019011 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(81): Show |
87 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.4066-82G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40019011 | |||||||
chr15:40019232 | C | T | 1 | a0003c0003t0002g0053 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4173+32C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019232 | |||||||
chr15:40019367 | A | G | 1 | a0002c0013t0001g0280 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4173+167A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019367 | |||||||
chr15:40019434 | C | T | 1 | a0001c0005t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4173+234C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019434 | |||||||
chr15:40019435 | C | T | 1 | a0001c0005t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4173+235C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019435 | |||||||
chr15:40019442 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4173+242G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019442 | |||||||
chr15:40019698 | C | T | 1 | a0001c0005t0005g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4173+498C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019698 | |||||||
chr15:40019699 | G | A | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4173+499G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019699 | |||||||
chr15:40020082 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4174-817G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020082 | |||||||
chr15:40020165 | C | CA | 223 | a0001c0001t0001g0001 a0001c0001t0001g0243 a0001c0001t0002g0009 others(220): Show |
228 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.4174-721dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020165 | ||||||
chr15:40020342 | A | AT | 8 | a0001c0001t0002g0144 a0001c0005t0005g0153 a0002c0002t0001g0159 others(5): Show |
8 | HG00741.hp1 HG02056.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4174-543dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020342 | ||||||
chr15:40020342 | AT | A | 6 | a0001c0001t0003g0012 a0001c0005t0001g0225 a0002c0004t0001g0324 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.4174-543delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020342 | ||||||
chr15:40020414 | A | G | 21 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0001c0001t0004g0244 others(18): Show |
23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4174-485A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020414 | |||||||
chr15:40020512 | A | ATATT | 4 | a0001c0001t0002g0111 a0001c0001t0002g0205 a0001c0021t0003g0223 others(1): Show |
4 | HG00621.hp1 HG02040.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.4174-361_4174-358d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | ||||||
chr15:40020512 | ATATT | A | 33 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.4174-361_4174-358d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | ||||||
chr15:40020512 | ATATTTAT others(1): Show |
A | 226 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(223): Show |
229 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.4174-365_4174-358d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | ||||||
chr15:40020520 | T | A | 29 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4174-379T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020520 | |||||||
chr15:40020524 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4174-375T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020524 | |||||||
chr15:40020528 | T | C | 3 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0162 |
3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4174-371T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020528 | |||||||
chr15:40020637 | G | A | 33 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.4174-262G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020637 | |||||||
chr15:40020682 | C | CT | 3 | a0002c0002t0007g0043 a0009c0016t0007g0042 a0009c0016t0007g0044 |
3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4174-216dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020682 | ||||||
chr15:40020721 | CT | C | 130 | a0001c0001t0001g0243 a0001c0001t0002g0009 a0001c0001t0002g0013 others(127): Show |
132 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.4174-162delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020721 | ||||||
chr15:40020811 | A | G | 2 | a0003c0003t0002g0055 a0003c0003t0002g0094 |
2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4174-88A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020811 | |||||||
chr15:40020882 | G | T | 274 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(271): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.4174-17G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020882 | |||||||
chr15:40021039 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4302+12A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021039 | |||||||
chr15:40021185 | A | G | 12 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0359 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.4302+158A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021185 | |||||||
chr15:40021473 | C | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4302+446C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021473 | |||||||
chr15:40021644 | A | C | 1 | a0002c0004t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4302+617A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021644 | |||||||
chr15:40021829 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4303-690C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021829 | |||||||
chr15:40021872 | G | C | 90 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0125 others(87): Show |
91 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.4303-647G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021872 | |||||||
chr15:40021990 | A | G | 73 | a0001c0005t0001g0032 a0001c0005t0001g0034 a0001c0005t0001g0132 others(70): Show |
74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.4303-529A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021990 | |||||||
chr15:40022181 | C | CGT | 13 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0206 others(10): Show |
14 | HG01168.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.4303-305_4303-304d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGT | 32 | a0001c0001t0001g0204 a0001c0001t0002g0148 a0001c0001t0003g0200 others(29): Show |
32 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.4303-307_4303-304d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGT | 26 | a0001c0001t0002g0129 a0001c0005t0001g0032 a0001c0005t0001g0034 others(23): Show |
26 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4303-309_4303-304d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGTG others(1): Show |
48 | a0001c0001t0002g0117 a0001c0001t0002g0140 a0001c0001t0002g0158 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.4303-311_4303-304d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGTG others(3): Show |
53 | a0001c0001t0001g0355 a0001c0001t0002g0118 a0001c0001t0002g0120 others(50): Show |
54 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.4303-313_4303-304d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGTG others(5): Show |
69 | a0001c0001t0001g0169 a0001c0001t0002g0119 a0001c0001t0002g0141 others(66): Show |
70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.4303-315_4303-304d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGTG others(7): Show |
5 | a0001c0001t0012g0155 a0002c0004t0001g0257 a0002c0004t0001g0328 others(2): Show |
5 | HG00544.hp1 HG01168.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303-317_4303-304d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022181 | C | CGTGTGTG others(9): Show |
8 | a0001c0005t0001g0180 a0001c0020t0001g0173 a0002c0004t0001g0209 others(5): Show |
8 | HG00621.hp2 HG01257.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.4303-319_4303-304d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | ||||||
chr15:40022196 | GTGTGTGT others(13): Show |
G | 1 | a0002c0029t0002g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4303-319_4303-300d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022196 | ||||||
chr15:40022206 | GTGTGTGT others(3): Show |
G | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4303-309_4303-300d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022206 | ||||||
chr15:40022208 | GTGTGTGT others(4): Show |
G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4303-305_4303-295d others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022208 | ||||||
chr15:40022214 | GTA | G | 6 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0219 others(3): Show |
6 | HG00597.hp1 HG03927.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303-303_4303-302d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022214 | ||||||
chr15:40022215 | TATG | T | 7 | a0001c0005t0001g0246 a0002c0004t0003g0036 a0002c0004t0003g0038 others(4): Show |
7 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-303_4303-301d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022215 | |||||||
chr15:40022216 | A | G | 119 | a0001c0001t0001g0243 a0001c0001t0002g0090 a0001c0001t0002g0117 others(116): Show |
121 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.4303-303A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022216 | |||||||
chr15:40022219 | T | G | 7 | a0001c0005t0001g0246 a0002c0004t0003g0036 a0002c0004t0003g0038 others(4): Show |
7 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-300T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022219 | |||||||
chr15:40022219 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0002g0090 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.4303-300_4303-299i others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022219 | |||||||
chr15:40022318 | G | C | 1 | a0004c0007t0002g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4303-201G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022318 | |||||||
chr15:40022325 | G | A | 252 | a0001c0001t0001g0169 a0001c0001t0001g0243 a0001c0001t0001g0355 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.4303-194G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022325 | |||||||
chr15:40022510 | T | G | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4303-9T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022510 | |||||||
chr15:40022683 | G | C | 4 | a0002c0004t0001g0271 a0002c0004t0003g0256 a0002c0004t0003g0263 others(1): Show |
4 | HG00544.hp2 HG02135.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.4389+78G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022683 | |||||||
chr15:40022741 | CT | C | 9 | a0001c0001t0003g0192 a0003c0003t0002g0104 a0003c0003t0003g0091 others(6): Show |
9 | HG02027.hp2 HG02523.hp2 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.4389+148delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40022741 | ||||||
chr15:40022766 | C | G | 205 | a0001c0001t0001g0133 a0001c0001t0001g0243 a0001c0001t0002g0009 others(202): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.4389+161C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022766 | |||||||
chr15:40022797 | A | T | 7 | a0001c0001t0001g0204 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.4389+192A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022797 | |||||||
chr15:40022819 | C | T | 1 | a0004c0007t0002g0266 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4389+214C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022819 | |||||||
chr15:40022873 | G | A | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389+268G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022873 | |||||||
chr15:40022884 | C | A | 1 | a0003c0003t0002g0103 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4389+279C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022884 | |||||||
chr15:40023016 | C | T | 2 | a0001c0001t0003g0192 a0001c0001t0003g0193 |
2 | NA19075.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4389+411C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023016 | |||||||
chr15:40023022 | C | T | 1 | a0002c0004t0002g0348 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4389+417C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023022 | |||||||
chr15:40023023 | G | A | 4 | a0002c0004t0003g0036 a0002c0004t0003g0039 a0002c0004t0005g0037 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+418G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023023 | |||||||
chr15:40023076 | T | G | 3 | a0002c0002t0007g0043 a0009c0016t0007g0042 a0009c0016t0007g0044 |
3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4389+471T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023076 | |||||||
chr15:40023179 | G | T | 1 | a0016c0034t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4389+574G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023179 | |||||||
chr15:40023195 | A | G | 4 | a0001c0001t0003g0002 a0001c0001t0003g0175 a0001c0001t0003g0226 others(1): Show |
5 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.4389+590A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023195 | |||||||
chr15:40023274 | T | C | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4389+669T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023274 | |||||||
chr15:40023335 | T | G | 6 | a0002c0002t0001g0359 a0002c0002t0001g0361 a0002c0002t0003g0161 others(3): Show |
6 | HG01109.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4389+730T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023335 | |||||||
chr15:40023416 | C | T | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+811C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023416 | |||||||
chr15:40023435 | A | G | 7 | a0001c0005t0001g0125 a0001c0005t0005g0123 a0001c0005t0005g0124 others(4): Show |
7 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4389+830A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023435 | |||||||
chr15:40023534 | A | G | 1 | a0003c0003t0002g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4389+929A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023534 | |||||||
chr15:40023675 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4389+1070C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023675 | |||||||
chr15:40023837 | C | CT | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389+1239dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40023837 | ||||||
chr15:40023967 | A | G | 3 | a0008c0015t0005g0026 a0008c0015t0006g0025 a0008c0015t0006g0027 |
3 | HG02976.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4389+1362A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023967 | |||||||
chr15:40023970 | A | C | 95 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4389+1365A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023970 | |||||||
chr15:40024161 | A | C | 1 | a0003c0003t0002g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4389+1556A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024161 | |||||||
chr15:40024218 | C | CT | 12 | a0002c0002t0002g0040 a0002c0002t0002g0308 a0002c0002t0002g0309 others(9): Show |
12 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4389+1623dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024218 | ||||||
chr15:40024228 | T | TAAGAGAT others(313): Show |
3 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0026t0001g0011 |
3 | HG02258.hp1 HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4389+1639_4389+164 others(324): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024228 | ||||||
chr15:40024228 | T | TAAGAGAT others(314): Show |
1 | a0003c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4389+1639_4389+164 others(325): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024228 | ||||||
chr15:40024403 | C | CT | 13 | a0001c0001t0001g0204 a0001c0001t0003g0186 a0001c0001t0003g0196 others(10): Show |
13 | HG01516.hp1 HG01884.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.4390-1551dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | ||||||
chr15:40024403 | CT | C | 90 | a0001c0001t0002g0013 a0001c0001t0002g0129 a0001c0001t0002g0138 others(87): Show |
92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.4390-1551delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | ||||||
chr15:40024403 | CTT | C | 10 | a0001c0001t0002g0009 a0001c0001t0002g0128 a0001c0001t0004g0194 others(7): Show |
10 | HG00597.hp2 HG01255.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.4390-1552_4390-155 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | ||||||
chr15:40024403 | CTTTTTTT | C | 24 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0035 others(21): Show |
24 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.4390-1557_4390-155 others(11): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | ||||||
chr15:40024479 | A | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4390-1498A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024479 | |||||||
chr15:40024649 | C | T | 102 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(99): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-1328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024649 | |||||||
chr15:40024677 | C | T | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1300C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024677 | |||||||
chr15:40024700 | C | CT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(142): Show |
150 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.4390-1264dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024700 | ||||||
chr15:40024737 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4390-1240T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024737 | |||||||
chr15:40024739 | G | GTT | 7 | a0002c0002t0001g0159 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02809.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4390-1228_4390-122 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024739 | ||||||
chr15:40024764 | A | T | 5 | a0002c0002t0001g0359 a0002c0002t0003g0161 a0002c0002t0003g0334 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4390-1213A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024764 | |||||||
chr15:40024782 | G | A | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1195G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024782 | |||||||
chr15:40024809 | A | G | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1168A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024809 | |||||||
chr15:40024874 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(117): Show |
125 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.4390-1103G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024874 | |||||||
chr15:40024916 | G | A | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1061G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024916 | |||||||
chr15:40025314 | C | T | 102 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(99): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-663C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025314 | |||||||
chr15:40025407 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.4390-570G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025407 | |||||||
chr15:40025500 | A | G | 1 | a0002c0004t0001g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4390-477A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025500 | |||||||
chr15:40025591 | T | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.4390-386T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025591 | |||||||
chr15:40025608 | A | G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(99): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-369A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025608 | |||||||
chr15:40025647 | TA | T | 22 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(19): Show |
22 | HG00438.hp2 HG02056.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.4390-318delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40025647 | ||||||
chr15:40025782 | G | A | 1 | a0004c0006t0001g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4390-195G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025782 | |||||||
chr15:40026111 | G | A | 8 | a0002c0002t0001g0159 a0003c0003t0003g0091 a0003c0025t0004g0010 others(5): Show |
8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4502+22G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026111 | |||||||
chr15:40026146 | C | G | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4502+57C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026146 | |||||||
chr15:40026187 | G | C | 9 | a0001c0001t0003g0245 a0002c0002t0001g0359 a0002c0002t0003g0161 others(6): Show |
9 | HG01081.hp1 HG02055.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.4502+98G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026187 | |||||||
chr15:40026264 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4502+175G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026264 | |||||||
chr15:40026289 | TA | T | 8 | a0002c0002t0001g0159 a0003c0003t0003g0091 a0003c0025t0004g0010 others(5): Show |
8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4502+210delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40026289 | ||||||
chr15:40026290 | A | G | 1 | a0001c0001t0001g0355 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4502+201A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026290 | |||||||
chr15:40026300 | T | A | 5 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4502+211T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026300 | |||||||
chr15:40026335 | A | G | 4 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+246A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026335 | |||||||
chr15:40026480 | A | G | 1 | a0003c0003t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4502+391A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026480 | |||||||
chr15:40026518 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4502+429C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026518 | |||||||
chr15:40026731 | T | C | 2 | a0002c0002t0001g0160 a0002c0002t0001g0162 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4502+642T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026731 | |||||||
chr15:40026887 | T | C | 5 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 others(2): Show |
5 | NA18984.hp1 NA19074.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.4502+798T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026887 | |||||||
chr15:40027102 | C | T | 1 | a0002c0002t0002g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4502+1013C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027102 | |||||||
chr15:40027150 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4502+1061C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027150 | |||||||
chr15:40027306 | T | C | 5 | a0002c0002t0001g0359 a0002c0002t0003g0161 a0002c0002t0003g0334 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4502+1217T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027306 | |||||||
chr15:40027316 | G | A | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+1227G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027316 | |||||||
chr15:40027432 | C | T | 1 | a0004c0007t0002g0262 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4502+1343C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027432 | |||||||
chr15:40027571 | TG | T | 14 | a0001c0001t0001g0243 a0001c0001t0003g0245 a0002c0002t0001g0035 others(11): Show |
14 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.4502+1483delG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027571 | |||||||
chr15:40027613 | G | A | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+1524G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027613 | |||||||
chr15:40027617 | G | A | 6 | a0003c0003t0002g0072 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.4502+1528G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027617 | |||||||
chr15:40027699 | G | A | 6 | a0003c0003t0003g0091 a0007c0009t0003g0229 a0007c0009t0003g0231 others(3): Show |
6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4502+1610G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027699 | |||||||
chr15:40027704 | C | T | 1 | a0002c0002t0002g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4502+1615C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027704 | |||||||
chr15:40027760 | G | A | 4 | a0001c0005t0001g0246 a0003c0010t0001g0047 a0003c0010t0001g0048 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4503-1646G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027760 | |||||||
chr15:40027845 | C | A | 95 | a0001c0001t0002g0090 a0001c0001t0002g0117 a0001c0001t0002g0118 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4503-1561C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027845 | |||||||
chr15:40027889 | C | CA | 39 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0001c0001t0002g0129 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.4503-1506dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40027889 | ||||||
chr15:40027900 | A | C | 8 | a0002c0002t0001g0159 a0003c0003t0003g0091 a0003c0025t0004g0010 others(5): Show |
8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4503-1506A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027900 | |||||||
chr15:40028031 | A | G | 29 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4503-1375A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028031 | |||||||
chr15:40028066 | A | G | 29 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0002c0002t0001g0003 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4503-1340A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028066 | |||||||
chr15:40028079 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(113): Show |
119 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.4503-1314dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40028079 | ||||||
chr15:40028081 | T | C | 1 | a0002c0002t0001g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4503-1325T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028081 | |||||||
chr15:40028114 | C | G | 1 | a0002c0002t0005g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4503-1292C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028114 | |||||||
chr15:40028114 | C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4503-1292C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028114 | |||||||
chr15:40028163 | C | T | 7 | a0001c0001t0001g0204 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.4503-1243C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028163 | |||||||
chr15:40028540 | T | C | 9 | a0001c0001t0003g0170 a0001c0001t0003g0172 a0001c0001t0003g0178 others(6): Show |
9 | HG02155.hp2 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.4503-866T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028540 | |||||||
chr15:40028565 | C | G | 2 | a0002c0004t0001g0303 a0002c0004t0001g0312 |
2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4503-841C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028565 | |||||||
chr15:40028632 | TC | T | 5 | a0001c0005t0001g0246 a0002c0002t0001g0159 a0003c0010t0001g0047 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-773delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028632 | |||||||
chr15:40028635 | C | T | 13 | a0001c0001t0002g0158 a0002c0002t0001g0160 a0002c0002t0001g0162 others(10): Show |
13 | HG00673.hp1 HG01099.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.4503-771C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028635 | |||||||
chr15:40028825 | G | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4503-581G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028825 | |||||||
chr15:40028871 | C | T | 5 | a0001c0005t0001g0246 a0002c0002t0001g0159 a0003c0010t0001g0047 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-535C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028871 | |||||||
chr15:40028882 | G | C | 1 | a0003c0003t0003g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4503-524G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028882 | |||||||
chr15:40028973 | G | A | 12 | a0001c0001t0002g0147 a0002c0004t0002g0311 a0003c0003t0002g0056 others(9): Show |
12 | HG00408.hp2 HG00544.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.4503-433G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028973 | |||||||
chr15:40029150 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(149): Show |
157 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.4503-256C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029150 | |||||||
chr15:40029235 | C | G | 5 | a0002c0002t0001g0359 a0002c0002t0003g0161 a0002c0002t0003g0334 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-171C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029235 | |||||||
chr15:40029240 | C | T | 2 | a0003c0003t0002g0055 a0003c0003t0002g0094 |
2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4503-166C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029240 | |||||||
chr15:40029331 | G | A | 7 | a0003c0003t0003g0091 a0003c0025t0004g0010 a0007c0009t0003g0229 others(4): Show |
7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4503-75G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029331 | |||||||
chr15:40029579 | C | T | 3 | a0004c0007t0002g0266 a0004c0007t0003g0258 a0011c0017t0003g0341 |
3 | HG03098.hp1 NA18972.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4561+115C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029579 | |||||||
chr15:40029731 | G | A | 1 | a0002c0002t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4561+267G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029731 | |||||||
chr15:40029923 | T | C | 36 | a0001c0001t0001g0169 a0001c0001t0001g0355 a0001c0001t0003g0002 others(33): Show |
38 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.4562-436T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029923 | |||||||
chr15:40029966 | C | T | 109 | a0001c0001t0001g0133 a0001c0001t0002g0009 a0001c0001t0002g0013 others(106): Show |
109 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.4562-393C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029966 | |||||||
chr15:40030095 | G | A | 4 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 others(1): Show |
4 | HG02965.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4562-264G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030095 | |||||||
chr15:40030198 | C | T | 1 | a0003c0003t0006g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4562-161C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030198 | |||||||
chr15:40030259 | C | T | 44 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0109 others(41): Show |
45 | HG00438.hp1 HG01256.hp1 HG01258.hp2 others(42): Show |
intron_variant | MODIFIER | c.4562-100C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030259 | |||||||
chr15:40030347 | T | G | 5 | a0001c0005t0001g0246 a0002c0002t0001g0159 a0003c0010t0001g0047 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4562-12T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030347 | |||||||
chr15:40030351 | G | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
splice_region_variant&intron_variant | LOW | c.4562-8G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030351 | |||||||
chr15:40030584 | T | C | 2 | a0002c0002t0002g0336 a0002c0002t0002g0337 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4659+128T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40030584 | |||||||
chr15:40031009 | G | A | 5 | a0001c0005t0001g0246 a0002c0002t0001g0159 a0003c0010t0001g0047 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4659+553G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031009 | |||||||
chr15:40031015 | G | A | 3 | a0004c0006t0006g0251 a0004c0006t0006g0252 a0004c0006t0006g0260 |
3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4659+559G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031015 | |||||||
chr15:40031037 | C | T | 10 | a0001c0001t0003g0208 a0001c0021t0003g0223 a0002c0002t0001g0359 others(7): Show |
10 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.4659+581C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031037 | |||||||
chr15:40031121 | T | C | 2 | a0002c0002t0004g0018 a0002c0002t0004g0019 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4659+665T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031121 | |||||||
chr15:40031197 | G | C | 120 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(117): Show |
120 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.4659+741G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031197 | |||||||
chr15:40031339 | G | A | 1 | a0014c0035t0003g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4660-830G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031339 | |||||||
chr15:40031392 | T | C | 1 | a0002c0004t0002g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4660-777T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031392 | |||||||
chr15:40031491 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(304): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.4660-678A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031491 | |||||||
chr15:40031508 | GCCAC | G | 3 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 |
3 | HG01891.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4660-659_4660-656d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 40031508 | ||||||
chr15:40031686 | C | T | 1 | a0002c0002t0001g0360 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4660-483C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031686 | |||||||
chr15:40031731 | C | CT | 22 | a0001c0001t0004g0194 a0001c0001t0004g0244 a0001c0005t0004g0121 others(19): Show |
24 | HG00408.hp1 HG01074.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.4660-426dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 40031731 | ||||||
chr15:40031731 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(80): Show |
85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.4660-438C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031731 | |||||||
chr15:40031874 | G | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.4660-295G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031874 | |||||||
chr15:40032079 | C | T | 1 | a0003c0003t0002g0100 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4660-90C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40032079 | |||||||
chr15:40032121 | A | G | 3 | a0002c0004t0003g0036 a0002c0004t0003g0038 a0002c0004t0003g0039 |
3 | HG01891.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4660-48A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40032121 | |||||||
chr15:40032280 | T | C | 116 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(113): Show |
116 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.4728+43T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032280 | |||||||
chr15:40032528 | G | A | 119 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(116): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.4729-229G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032528 | |||||||
chr15:40032592 | C | T | 1 | a0002c0002t0001g0361 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4729-165C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032592 | |||||||
chr15:40032604 | C | G | 1 | a0004c0006t0001g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4729-153C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032604 | |||||||
chr15:40032626 | A | C | 9 | a0001c0001t0003g0208 a0001c0021t0003g0223 a0003c0003t0003g0060 others(6): Show |
9 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.4729-131A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032626 | |||||||
chr15:40032636 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(303): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.4729-121C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032636 | |||||||
chr15:40033147 | T | C | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4773+346T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033147 | |||||||
chr15:40033267 | G | A | 21 | a0001c0001t0005g0014 a0001c0001t0005g0023 a0001c0001t0005g0028 others(18): Show |
21 | HG00741.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.4773+466G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033267 | |||||||
chr15:40033293 | A | C | 2 | a0008c0015t0006g0025 a0008c0015t0006g0027 |
2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4773+492A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033293 | |||||||
chr15:40033490 | C | T | 119 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(116): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.4773+689C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033490 | |||||||
chr15:40033628 | T | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(304): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.4774-698T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033628 | |||||||
chr15:40033629 | T | C | 1 | a0002c0004t0001g0319 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4774-697T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033629 | |||||||
chr15:40033659 | A | G | 164 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0090 others(161): Show |
166 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.4774-667A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033659 | |||||||
chr15:40033706 | T | G | 1 | a0016c0034t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4774-620T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033706 | |||||||
chr15:40033721 | A | G | 3 | a0002c0002t0003g0161 a0002c0002t0003g0334 a0002c0002t0003g0335 |
3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-605A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033721 | |||||||
chr15:40033821 | G | A | 9 | a0001c0001t0003g0208 a0001c0021t0003g0223 a0003c0003t0003g0060 others(6): Show |
9 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-505G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033821 | |||||||
chr15:40033848 | G | A | 1 | a0009c0016t0007g0042 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4774-478G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033848 | |||||||
chr15:40033849 | A | G | 5 | a0001c0005t0001g0246 a0002c0002t0001g0159 a0003c0010t0001g0047 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-477A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033849 | |||||||
chr15:40033977 | G | A | 2 | a0002c0004t0001g0319 a0004c0006t0001g0261 |
2 | HG01981.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.4774-349G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033977 | |||||||
chr15:40034015 | C | T | 3 | a0004c0006t0006g0251 a0004c0006t0006g0252 a0004c0006t0006g0260 |
3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4774-311C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40034015 | |||||||
chr15:40034028 | CA | C | 14 | a0001c0001t0003g0208 a0001c0001t0012g0155 a0001c0005t0005g0124 others(11): Show |
14 | HG01109.hp2 HG01975.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-279delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 40034028 | ||||||
chr15:40034166 | A | G | 1 | a0003c0010t0001g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4774-160A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40034166 | |||||||
chr15:40034552 | C | A | 1 | a0001c0005t0004g0121 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4892+108C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | chr15 | 40034552 | |||||||
chr15:40034943 | C | CT | 5 | a0001c0001t0002g0128 a0003c0003t0002g0054 a0003c0003t0002g0070 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.4893-83dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 40034943 | ||||||
chr15:40035004 | A | T | 1 | a0001c0001t0003g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4893-23A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | chr15 | 40035004 | |||||||
chr15:40035006 | ATCTTT | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0116 others(16): Show |
21 | HG00609.hp1 HG00609.hp2 HG01168.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.4893-9_4893-5delCT others(3): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 40035006 |