Item | Value |
---|---|
geneid | 79993 |
ensemblid | ENSG00000164181.14 |
hgncid | 26292 |
symbol | ELOVL7 |
name | ELOVL fatty acid elongase 7 |
refseq_nuc | NM_024930.3 |
refseq_prot | NP_079206.2 |
ensembl_nuc | ENST00000508821.6 |
ensembl_prot | ENSP00000424123.1 |
mane_status | MANE Select |
chr | chr5 |
start | 60751791 |
end | 60844269 |
strand | - |
ver | v1.2 |
region | chr5:60751791-60844269 |
region5000 | chr5:60746791-60849269 |
regionname0 | ELOVL7_chr5_60751791_60844269 |
regionname5000 | ELOVL7_chr5_60746791_60849269 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 281 | 255 | 80 | 46 | 79 | 16 | 32 | 58 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | MAFSD others(276): Show |
chr5 | 60746791 | 60849269 |
a0002 | 0/0 | 281 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | MAFSD others(276): Show |
chr5 | 60746791 | 60849269 |
a0003 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | MAFSD others(276): Show |
chr5 | 60746791 | 60849269 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 843 | 254 | 79 | 46 | 79 | 16 | 32 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | ATGGC others(838): Show |
chr5 | 60746791 | 60849269 | ||
a0001c0003 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | ATGGC others(838): Show |
chr5 | 60746791 | 60849269 | ||
a0002c0002 | 0/0 | 843 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | ATGGC others(838): Show |
chr5 | 60746791 | 60849269 | ||
a0003c0004 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | ATGGC others(838): Show |
chr5 | 60746791 | 60849269 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3874 | 71 | 11 | 16 | 30 | 6 | 7 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0002 | 0/0 | 3874 | 46 | 2 | 5 | 29 | 0 | 10 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0003 | 0/0 | 3874 | 43 | 34 | 2 | 2 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0004 | 0/0 | 3875 | 23 | 0 | 3 | 16 | 2 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3870): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0005 | 0/0 | 3874 | 18 | 6 | 7 | 0 | 3 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0006 | 0/0 | 3875 | 11 | 9 | 0 | 0 | 0 | 2 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3870): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0007 | 0/0 | 3874 | 9 | 0 | 3 | 0 | 1 | 5 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0008 | 0/0 | 3874 | 8 | 8 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0009 | 1/0 | 3874 | 4 | 0 | 2 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0010 | 0/0 | 3874 | 4 | 0 | 3 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0011 | 0/0 | 3874 | 2 | 1 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0012 | 0/0 | 3874 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0013 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0014 | 0/0 | 3874 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0015 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0016 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3870): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0017 | 0/0 | 3874 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0018 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0019 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0020 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0021 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0022 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0023 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3870): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0024 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0001t0025 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0001c0003t0006 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3870): Show |
chr5 | 60746791 | 60849269 |
a0002c0002t0001 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0002c0002t0002 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
a0003c0004t0001 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | AGTCG others(3869): Show |
chr5 | 60746791 | 60849269 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0010g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0011g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0012g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0012g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0014g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0019g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0022g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0023g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0024g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0001t0025g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0001c0003t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0010 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0246 | EUR | GBR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0033 | EUR | FIN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00735 | hp1 | a0001 | c0001 | t0010 | g0245 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01074 | hp2 | a0001 | c0001 | t0010 | g0247 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01099 | hp2 | a0001 | c0001 | t0014 | g0025 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0201 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01175 | hp2 | a0001 | c0001 | t0023 | g0162 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0241 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0249 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01433 | hp1 | a0001 | c0001 | t0012 | g0242 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0031 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0056 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0180 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0012 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0179 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01981 | hp1 | a0001 | c0001 | t0009 | g0243 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG01981 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0128 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02615 | hp1 | a0001 | c0001 | t0025 | g0161 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0133 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02717 | hp1 | a0001 | c0001 | t0022 | g0175 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0163 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02809 | hp1 | a0001 | c0003 | t0006 | g0139 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02896 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0200 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03579 | hp2 | a0001 | c0001 | t0021 | g0194 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0057 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0250 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0029 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0032 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0202 | SAS | BEB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04228 | hp1 | a0001 | c0001 | t0017 | g0035 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0215 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19000 | hp2 | a0001 | c0001 | t0019 | g0041 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19030 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | LWK | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19063 | hp2 | a0003 | c0004 | t0001 | g0086 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20129 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | ASW | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | ASW | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0116 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0013 | EUR | TSI | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | GIH | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0203 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | USA | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0244 | REF | REF | ELOVL7_chr5_60746791_60849269 | ELOVL7 | chr5 | 60746791 | 60849269 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60754695 | G | A | 1 | a0002 | 2 | HG00544.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.775C>T | p.Arg259Cys | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 970/3874 | 775/846 | 259/281 | chr5 | 60754695 | |||
chr5:60771949 | G | A | 1 | a0003 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.209C>T | p.Thr70Met | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/9 | 404/3874 | 209/846 | 70/281 | chr5 | 60771949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60772059 | C | T | 1 | a0001c0003 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.99G>A | p.Ser33Ser | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/9 | 294/3874 | 99/846 | 33/281 | chr5 | 60772059 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60751935 | A | C | 1 | a0001c0001t0017 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2689T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2689 | chr5 | 60751935 | ||||||
chr5:60751945 | T | C | 1 | a0001c0001t0021 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2679A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2679 | chr5 | 60751945 | ||||||
chr5:60751988 | T | C | 2 | a0001c0001t0013 a0001c0001t0022 |
2 | HG02717.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2636 | chr5 | 60751988 | ||||||
chr5:60752051 | A | G | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02572.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2573T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2573 | chr5 | 60752051 | ||||||
chr5:60752147 | T | A | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(2): Show |
60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2477A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2477 | chr5 | 60752147 | ||||||
chr5:60752201 | G | A | 5 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(2): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2423C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2423 | chr5 | 60752201 | ||||||
chr5:60752428 | T | C | 1 | a0001c0001t0023 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2196 | chr5 | 60752428 | ||||||
chr5:60752601 | T | C | 1 | a0001c0001t0024 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 2023 | chr5 | 60752601 | ||||||
chr5:60752846 | G | A | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1778 | chr5 | 60752846 | ||||||
chr5:60752909 | C | A | 1 | a0001c0001t0014 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1715 | chr5 | 60752909 | ||||||
chr5:60752945 | G | GA | 3 | a0001c0001t0006 a0001c0001t0023 a0001c0003t0006 |
13 | HG01175.hp2 HG02615.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1678dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1678 | chr5 | 60752945 | ||||||
chr5:60752952 | A | AT | 2 | a0001c0001t0004 a0001c0001t0016 |
24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1671 | chr5 | 60752952 | ||||||
chr5:60753047 | A | G | 1 | a0001c0001t0019 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1577 | chr5 | 60753047 | ||||||
chr5:60753292 | T | C | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0015 |
46 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1332A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1332 | chr5 | 60753292 | ||||||
chr5:60753413 | G | A | 1 | a0001c0001t0008 | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1211C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 1211 | chr5 | 60753413 | ||||||
chr5:60753750 | G | C | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(2): Show |
60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*874C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 874 | chr5 | 60753750 | ||||||
chr5:60753926 | G | A | 1 | a0001c0001t0011 | 2 | HG01109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 698 | chr5 | 60753926 | ||||||
chr5:60754220 | C | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 404 | chr5 | 60754220 | ||||||
chr5:60754266 | C | A | 1 | a0001c0001t0025 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 9/9 | 358 | chr5 | 60754266 | ||||||
chr5:60844188 | G | A | 1 | a0001c0001t0012 | 2 | HG01192.hp1 HG01433.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56791 | chr5 | 60844188 | ||||||
chr5:60844234 | T | C | 3 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 |
11 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-160A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56837 | chr5 | 60844234 | ||||||
chr5:60844250 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-176G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56853 | chr5 | 60844250 | ||||||
chr5:60844259 | G | T | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(4): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-185C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/9 | 56862 | chr5 | 60844259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:60755410 | G | A | 1 | a0001c0001t0005g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.637-577C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755410 | |||||||
chr5:60755514 | G | A | 2 | a0001c0001t0001g0085 a0003c0004t0001g0086 |
2 | NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.637-681C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755514 | |||||||
chr5:60755595 | T | G | 1 | a0001c0001t0003g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.637-762A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755595 | |||||||
chr5:60755773 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-940C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755773 | |||||||
chr5:60755912 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637-1079A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60755912 | |||||||
chr5:60756010 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-1177A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756010 | |||||||
chr5:60756132 | AG | A | 48 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.637-1300delC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756132 | |||||||
chr5:60756181 | A | C | 1 | a0001c0001t0002g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.636+1328T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756181 | |||||||
chr5:60756245 | TAAATAC | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+1258_636+1263d others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756245 | |||||||
chr5:60756423 | A | T | 1 | a0001c0001t0003g0007 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.636+1086T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756423 | |||||||
chr5:60756575 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.636+934A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756575 | |||||||
chr5:60756742 | C | A | 44 | a0001c0001t0003g0007 a0001c0001t0003g0038 a0001c0001t0003g0051 others(41): Show |
45 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.636+767G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756742 | |||||||
chr5:60756792 | A | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.636+717T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756792 | |||||||
chr5:60756816 | G | A | 90 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(87): Show |
93 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.636+693C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756816 | |||||||
chr5:60756829 | A | T | 1 | a0001c0001t0004g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.636+680T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60756829 | |||||||
chr5:60757103 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.636+406A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757103 | |||||||
chr5:60757280 | A | T | 9 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0071 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+229T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757280 | |||||||
chr5:60757354 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.636+155T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757354 | |||||||
chr5:60757366 | A | G | 1 | a0001c0001t0004g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.636+143T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757366 | |||||||
chr5:60757393 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
13 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.636+116G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757393 | |||||||
chr5:60757395 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.636+114G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 8/8 | chr5 | 60757395 | |||||||
chr5:60757950 | A | G | 1 | a0001c0001t0005g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500-305T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60757950 | |||||||
chr5:60758707 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0221 a0001c0001t0002g0225 others(1): Show |
5 | HG00621.hp1 NA18945.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1062C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758707 | |||||||
chr5:60758733 | C | T | 1 | a0001c0001t0008g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.500-1088G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758733 | |||||||
chr5:60758771 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.500-1126C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758771 | |||||||
chr5:60758799 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.500-1154A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60758799 | |||||||
chr5:60759104 | C | G | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-1459G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759104 | |||||||
chr5:60759293 | C | T | 1 | a0001c0001t0010g0245 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.500-1648G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759293 | |||||||
chr5:60759409 | AAATAG | A | 10 | a0001c0001t0002g0054 a0001c0001t0002g0102 a0001c0001t0002g0206 others(7): Show |
10 | HG02135.hp1 NA18939.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-1769_500-1765d others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759409 | |||||||
chr5:60759573 | C | A | 1 | a0001c0001t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500-1928G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759573 | |||||||
chr5:60759608 | C | CT | 148 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(145): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.500-1964dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759608 | |||||||
chr5:60759677 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-2032C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759677 | |||||||
chr5:60759784 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.500-2139A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759784 | |||||||
chr5:60759817 | T | A | 22 | a0001c0001t0003g0038 a0001c0001t0003g0144 a0001c0001t0003g0146 others(19): Show |
22 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.500-2172A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60759817 | |||||||
chr5:60760028 | C | T | 25 | a0001c0001t0001g0099 a0001c0001t0001g0152 a0001c0001t0001g0165 others(22): Show |
25 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.500-2383G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760028 | |||||||
chr5:60760086 | C | T | 59 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0054 others(56): Show |
60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.500-2441G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760086 | |||||||
chr5:60760282 | G | A | 1 | a0001c0001t0004g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.500-2637C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760282 | |||||||
chr5:60760410 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.500-2765A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760410 | |||||||
chr5:60760699 | C | T | 2 | a0001c0001t0020g0128 a0001c0001t0021g0194 |
2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.500-3054G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760699 | |||||||
chr5:60760762 | C | T | 151 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(148): Show |
155 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.500-3117G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60760762 | |||||||
chr5:60761037 | A | ATGTT | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3189_499+3190i others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761037 | |||||||
chr5:60761156 | G | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3071C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761156 | |||||||
chr5:60761173 | T | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+3054A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761173 | |||||||
chr5:60761343 | C | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(2): Show |
5 | NA18939.hp1 NA18951.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+2884G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761343 | |||||||
chr5:60761460 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(244): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.499+2767G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761460 | |||||||
chr5:60761572 | C | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+2655G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761572 | |||||||
chr5:60761699 | A | G | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.499+2528T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761699 | |||||||
chr5:60761725 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.499+2502G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761725 | |||||||
chr5:60761891 | C | T | 7 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(4): Show |
9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.499+2336G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761891 | |||||||
chr5:60761956 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.499+2271G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761956 | |||||||
chr5:60761957 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.499+2270C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761957 | |||||||
chr5:60761991 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.499+2236A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60761991 | |||||||
chr5:60762009 | T | C | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.499+2218A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762009 | |||||||
chr5:60762046 | T | C | 46 | a0001c0001t0003g0007 a0001c0001t0003g0038 a0001c0001t0003g0051 others(43): Show |
47 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.499+2181A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762046 | |||||||
chr5:60762048 | A | G | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+2179T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762048 | |||||||
chr5:60762105 | A | G | 50 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(47): Show |
51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.499+2122T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762105 | |||||||
chr5:60762166 | G | C | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.499+2061C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762166 | |||||||
chr5:60762213 | C | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.499+2014G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762213 | |||||||
chr5:60762231 | G | A | 2 | a0001c0001t0003g0160 a0001c0001t0003g0164 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.499+1996C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762231 | |||||||
chr5:60762255 | C | T | 6 | a0001c0001t0003g0151 a0001c0001t0003g0191 a0001c0001t0003g0192 others(3): Show |
6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+1972G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762255 | |||||||
chr5:60762299 | C | CA | 13 | a0001c0001t0001g0093 a0001c0001t0001g0236 a0001c0001t0002g0213 others(10): Show |
13 | HG01069.hp2 HG01175.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.499+1927dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | |||||||
chr5:60762299 | CA | C | 12 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0066 others(9): Show |
12 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.499+1927delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | |||||||
chr5:60762299 | CAA | C | 49 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(46): Show |
50 | HG00099.hp2 HG00673.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.499+1926_499+1927d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | |||||||
chr5:60762299 | CAAA | C | 40 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(37): Show |
42 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+1925_499+1927d others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762299 | |||||||
chr5:60762426 | C | T | 31 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(28): Show |
33 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.499+1801G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762426 | |||||||
chr5:60762429 | A | G | 2 | a0001c0001t0006g0140 a0001c0003t0006g0139 |
2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.499+1798T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762429 | |||||||
chr5:60762463 | T | C | 2 | a0001c0001t0012g0241 a0001c0001t0012g0242 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.499+1764A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762463 | |||||||
chr5:60762571 | C | T | 50 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(47): Show |
51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.499+1656G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762571 | |||||||
chr5:60762625 | G | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+1602C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60762625 | |||||||
chr5:60763031 | C | T | 185 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(182): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.499+1196G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763031 | |||||||
chr5:60763160 | A | G | 49 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(46): Show |
50 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.499+1067T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763160 | |||||||
chr5:60763305 | T | C | 49 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(46): Show |
50 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.499+922A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60763305 | |||||||
chr5:60764181 | T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+46A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 7/8 | chr5 | 60764181 | |||||||
chr5:60764645 | T | TA | 59 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0054 others(56): Show |
60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.394-314dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764645 | |||||||
chr5:60764729 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-397A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764729 | |||||||
chr5:60764870 | C | T | 28 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(25): Show |
30 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.394-538G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60764870 | |||||||
chr5:60765063 | G | A | 8 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(5): Show |
8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-731C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765063 | |||||||
chr5:60765135 | G | C | 8 | a0001c0001t0003g0151 a0001c0001t0003g0172 a0001c0001t0003g0174 others(5): Show |
8 | HG00099.hp2 HG02145.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-803C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765135 | |||||||
chr5:60765190 | A | C | 2 | a0001c0001t0020g0128 a0001c0001t0021g0194 |
2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.394-858T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765190 | |||||||
chr5:60765230 | G | A | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394-898C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765230 | |||||||
chr5:60765285 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-953C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765285 | |||||||
chr5:60765329 | A | G | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-997T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765329 | |||||||
chr5:60765594 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.393+980C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765594 | |||||||
chr5:60765659 | C | T | 34 | a0001c0001t0001g0099 a0001c0001t0001g0152 a0001c0001t0001g0165 others(31): Show |
36 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.393+915G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765659 | |||||||
chr5:60765727 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+847A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765727 | |||||||
chr5:60765729 | G | C | 59 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0054 others(56): Show |
60 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.393+845C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765729 | |||||||
chr5:60765976 | G | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+598C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60765976 | |||||||
chr5:60766103 | C | T | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+471G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766103 | |||||||
chr5:60766266 | T | C | 2 | a0001c0001t0012g0241 a0001c0001t0012g0242 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.393+308A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766266 | |||||||
chr5:60766332 | G | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.393+242C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766332 | |||||||
chr5:60766347 | T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.393+227A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 6/8 | chr5 | 60766347 | |||||||
chr5:60766777 | C | T | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.337-147G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766777 | |||||||
chr5:60766791 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.337-161A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766791 | |||||||
chr5:60766797 | C | A | 48 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.337-167G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766797 | |||||||
chr5:60766804 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337-174A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766804 | |||||||
chr5:60766841 | C | T | 48 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.337-211G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766841 | |||||||
chr5:60766913 | G | A | 8 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(5): Show |
8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-283C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766913 | |||||||
chr5:60766918 | T | C | 184 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.337-288A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60766918 | |||||||
chr5:60767067 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.337-437T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767067 | |||||||
chr5:60767185 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.337-555A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767185 | |||||||
chr5:60767358 | C | T | 2 | a0001c0001t0013g0009 a0001c0001t0022g0175 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.336+465G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767358 | |||||||
chr5:60767369 | C | A | 9 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0071 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+454G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767369 | |||||||
chr5:60767485 | C | T | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.336+338G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767485 | |||||||
chr5:60767676 | T | G | 1 | a0001c0001t0005g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.336+147A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767676 | |||||||
chr5:60767684 | G | T | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.336+139C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767684 | |||||||
chr5:60767749 | G | A | 184 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.336+74C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 5/8 | chr5 | 60767749 | |||||||
chr5:60767936 | A | C | 2 | a0001c0001t0020g0128 a0001c0001t0021g0194 |
2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.256-33T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60767936 | |||||||
chr5:60768085 | T | G | 3 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.256-182A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768085 | |||||||
chr5:60768126 | C | T | 184 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.256-223G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768126 | |||||||
chr5:60768510 | G | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-607C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768510 | |||||||
chr5:60768558 | C | T | 48 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.256-655G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768558 | |||||||
chr5:60768784 | C | T | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.256-881G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768784 | |||||||
chr5:60768805 | CT | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-903delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60768805 | |||||||
chr5:60769017 | A | G | 50 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(47): Show |
51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.256-1114T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769017 | |||||||
chr5:60769211 | G | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.256-1308C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769211 | |||||||
chr5:60769692 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0068 others(38): Show |
42 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.256-1789C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769692 | |||||||
chr5:60769778 | A | G | 1 | a0001c0001t0005g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.256-1875T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769778 | |||||||
chr5:60769855 | G | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.256-1952C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769855 | |||||||
chr5:60769858 | T | C | 15 | a0001c0001t0003g0038 a0001c0001t0003g0144 a0001c0001t0003g0146 others(12): Show |
15 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.256-1955A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769858 | |||||||
chr5:60769908 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.255+1995T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60769908 | |||||||
chr5:60770006 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.255+1897C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770006 | |||||||
chr5:60770029 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1874A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770029 | |||||||
chr5:60770053 | G | GA | 61 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.255+1849dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770053 | |||||||
chr5:60770053 | GA | G | 90 | a0001c0001t0001g0100 a0001c0001t0001g0122 a0001c0001t0001g0123 others(87): Show |
93 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.255+1849delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770053 | |||||||
chr5:60770114 | G | T | 48 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.255+1789C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770114 | |||||||
chr5:60770242 | C | T | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1661G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770242 | |||||||
chr5:60770498 | C | G | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1405G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770498 | |||||||
chr5:60770669 | T | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+1234A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770669 | |||||||
chr5:60770683 | A | C | 41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
43 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.255+1220T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770683 | |||||||
chr5:60770749 | G | A | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+1154C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770749 | |||||||
chr5:60770839 | G | A | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+1064C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60770839 | |||||||
chr5:60771017 | A | G | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+886T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771017 | |||||||
chr5:60771023 | C | T | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+880G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771023 | |||||||
chr5:60771114 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.255+789G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771114 | |||||||
chr5:60771140 | C | A | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.255+763G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771140 | |||||||
chr5:60771225 | A | C | 1 | a0001c0001t0003g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.255+678T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771225 | |||||||
chr5:60771357 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.255+546A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771357 | |||||||
chr5:60771723 | C | T | 35 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.255+180G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771723 | |||||||
chr5:60771877 | C | T | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.255+26G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771877 | |||||||
chr5:60771891 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.255+12C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 4/8 | chr5 | 60771891 | |||||||
chr5:60772520 | G | A | 50 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0003g0007 others(47): Show |
51 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-427C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772520 | |||||||
chr5:60772528 | T | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0068 others(54): Show |
58 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.65-435A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772528 | |||||||
chr5:60772807 | T | C | 91 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.65-714A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60772807 | |||||||
chr5:60773040 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-947C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773040 | |||||||
chr5:60773230 | C | T | 87 | a0001c0001t0001g0099 a0001c0001t0001g0165 a0001c0001t0001g0166 others(84): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.65-1137G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773230 | |||||||
chr5:60773327 | G | A | 1 | a0001c0001t0004g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.65-1234C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773327 | |||||||
chr5:60773340 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65-1247A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773340 | |||||||
chr5:60773510 | T | C | 1 | a0001c0001t0017g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-1417A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773510 | |||||||
chr5:60773612 | C | T | 7 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(4): Show |
9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-1519G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60773612 | |||||||
chr5:60774054 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.65-1961A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774054 | |||||||
chr5:60774094 | A | C | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.65-2001T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774094 | |||||||
chr5:60774107 | G | A | 146 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-2014C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774107 | |||||||
chr5:60774128 | A | G | 3 | a0001c0001t0004g0005 a0001c0001t0004g0037 a0001c0001t0016g0030 |
4 | HG01258.hp1 HG01496.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2035T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774128 | |||||||
chr5:60774228 | T | A | 7 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(4): Show |
9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-2135A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774228 | |||||||
chr5:60774275 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.65-2182C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774275 | |||||||
chr5:60774605 | T | G | 1 | a0001c0001t0004g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.65-2512A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774605 | |||||||
chr5:60774677 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.65-2584A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774677 | |||||||
chr5:60774764 | C | CT | 13 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0123 others(10): Show |
13 | HG01109.hp1 HG01258.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-2672dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774764 | |||||||
chr5:60774764 | C | CTT | 8 | a0001c0001t0001g0108 a0001c0001t0006g0138 a0001c0001t0006g0140 others(5): Show |
8 | HG01175.hp2 HG03098.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-2673_65-2672dup others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774764 | |||||||
chr5:60774766 | T | C | 1 | a0001c0001t0005g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.65-2673A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60774766 | |||||||
chr5:60775074 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.65-2981A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775074 | |||||||
chr5:60775291 | T | C | 1 | a0001c0001t0012g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-3198A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775291 | |||||||
chr5:60775452 | A | AT | 54 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(51): Show |
55 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.65-3360dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775452 | |||||||
chr5:60775682 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-3589T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775682 | |||||||
chr5:60775784 | G | A | 3 | a0001c0001t0010g0245 a0001c0001t0010g0246 a0001c0001t0010g0247 |
3 | HG00140.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.65-3691C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775784 | |||||||
chr5:60775813 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.65-3720A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775813 | |||||||
chr5:60775954 | C | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.65-3861G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60775954 | |||||||
chr5:60776220 | C | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0187 |
2 | NA18997.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.65-4127G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776220 | |||||||
chr5:60776650 | A | G | 68 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(65): Show |
69 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-4557T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776650 | |||||||
chr5:60776908 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-4815A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776908 | |||||||
chr5:60776952 | A | G | 33 | a0001c0001t0001g0099 a0001c0001t0001g0137 a0001c0001t0001g0166 others(30): Show |
35 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.65-4859T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60776952 | |||||||
chr5:60777190 | C | G | 10 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(7): Show |
10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5097G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777190 | |||||||
chr5:60777281 | AC | A | 10 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(7): Show |
10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5189delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777281 | |||||||
chr5:60777311 | T | C | 10 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(7): Show |
10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5218A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777311 | |||||||
chr5:60777382 | TA | T | 7 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(4): Show |
7 | HG02615.hp1 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-5290delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777382 | |||||||
chr5:60777392 | A | T | 54 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(51): Show |
55 | HG00673.hp1 HG01109.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.65-5299T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777392 | |||||||
chr5:60777398 | A | T | 32 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(29): Show |
34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.65-5305T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777398 | |||||||
chr5:60777492 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-5399G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60777492 | |||||||
chr5:60778173 | T | C | 146 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-6080A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778173 | |||||||
chr5:60778348 | C | G | 1 | a0001c0001t0005g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.65-6255G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778348 | |||||||
chr5:60778368 | C | G | 3 | a0001c0001t0003g0199 a0001c0001t0011g0200 a0001c0001t0011g0201 |
3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.65-6275G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778368 | |||||||
chr5:60778391 | C | T | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.65-6298G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778391 | |||||||
chr5:60778669 | C | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-6576G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60778669 | |||||||
chr5:60779260 | G | T | 10 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(7): Show |
10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-7167C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779260 | |||||||
chr5:60779366 | C | T | 43 | a0001c0001t0002g0112 a0001c0001t0002g0205 a0001c0001t0002g0206 others(40): Show |
43 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.65-7273G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779366 | |||||||
chr5:60779481 | A | T | 9 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(6): Show |
9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-7388T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779481 | |||||||
chr5:60779501 | C | T | 146 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.65-7408G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779501 | |||||||
chr5:60779688 | T | C | 9 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(6): Show |
9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-7595A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60779688 | |||||||
chr5:60780114 | C | CT | 9 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0001g0216 others(6): Show |
9 | HG00140.hp1 HG00438.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7219dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | |||||||
chr5:60780114 | CT | C | 5 | a0001c0001t0001g0098 a0001c0001t0002g0208 a0001c0001t0006g0163 others(2): Show |
5 | HG01257.hp1 HG02572.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7219delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | |||||||
chr5:60780114 | CTT | C | 62 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(59): Show |
63 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.64+7218_64+7219del others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780114 | |||||||
chr5:60780149 | C | T | 7 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(4): Show |
9 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7185G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780149 | |||||||
chr5:60780188 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0197 |
2 | HG01433.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.64+7146G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780188 | |||||||
chr5:60780189 | G | A | 32 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(29): Show |
34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+7145C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780189 | |||||||
chr5:60780530 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.64+6804C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780530 | |||||||
chr5:60780531 | C | T | 1 | a0001c0001t0003g0007 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64+6803G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780531 | |||||||
chr5:60780717 | G | T | 2 | a0001c0001t0012g0241 a0001c0001t0012g0242 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.64+6617C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780717 | |||||||
chr5:60780793 | C | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+6541G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60780793 | |||||||
chr5:60781012 | C | A | 3 | a0001c0001t0002g0204 a0001c0001t0003g0169 a0001c0001t0008g0203 |
3 | HG01167.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.64+6322G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781012 | |||||||
chr5:60781096 | G | T | 9 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(6): Show |
9 | HG01175.hp2 HG02735.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+6238C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781096 | |||||||
chr5:60781212 | G | GA | 35 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(32): Show |
37 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.64+6121dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781212 | |||||||
chr5:60781212 | GA | G | 12 | a0001c0001t0001g0125 a0001c0001t0006g0138 a0001c0001t0006g0140 others(9): Show |
12 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+6121delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781212 | |||||||
chr5:60781385 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.64+5949C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781385 | |||||||
chr5:60781460 | GA | G | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+5873delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781460 | |||||||
chr5:60781627 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0118 |
3 | HG02896.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64+5707G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60781627 | |||||||
chr5:60782022 | A | C | 1 | a0001c0001t0005g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.64+5312T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782022 | |||||||
chr5:60782085 | T | G | 146 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64+5249A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782085 | |||||||
chr5:60782585 | C | T | 146 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64+4749G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782585 | |||||||
chr5:60782745 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4589T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782745 | |||||||
chr5:60782746 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4588A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782746 | |||||||
chr5:60782748 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4586T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782748 | |||||||
chr5:60782758 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64+4576T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782758 | |||||||
chr5:60782766 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64+4568A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782766 | |||||||
chr5:60782879 | A | G | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+4455T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60782879 | |||||||
chr5:60783231 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+4103A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783231 | |||||||
chr5:60783404 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64+3930G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783404 | |||||||
chr5:60783543 | T | C | 1 | a0001c0001t0008g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+3791A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783543 | |||||||
chr5:60783554 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0121 |
3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.64+3780T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783554 | |||||||
chr5:60783873 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+3461T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783873 | |||||||
chr5:60783995 | C | A | 10 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(7): Show |
10 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+3339G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60783995 | |||||||
chr5:60784300 | C | T | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+3034G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784300 | |||||||
chr5:60784354 | G | A | 15 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(12): Show |
15 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+2980C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784354 | |||||||
chr5:60784512 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64+2822G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784512 | |||||||
chr5:60784547 | A | G | 53 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(50): Show |
54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+2787T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784547 | |||||||
chr5:60784567 | C | G | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+2767G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784567 | |||||||
chr5:60784591 | G | T | 53 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(50): Show |
54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+2743C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784591 | |||||||
chr5:60784596 | C | T | 32 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(29): Show |
34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+2738G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784596 | |||||||
chr5:60784789 | G | A | 12 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(9): Show |
12 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+2545C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60784789 | |||||||
chr5:60785008 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64+2326C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785008 | |||||||
chr5:60785028 | T | C | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+2306A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785028 | |||||||
chr5:60785052 | C | T | 3 | a0001c0001t0003g0199 a0001c0001t0011g0200 a0001c0001t0011g0201 |
3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.64+2282G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785052 | |||||||
chr5:60785198 | C | T | 32 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(29): Show |
34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+2136G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785198 | |||||||
chr5:60785469 | T | C | 53 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(50): Show |
54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1865A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785469 | |||||||
chr5:60785491 | T | C | 32 | a0001c0001t0001g0099 a0001c0001t0001g0166 a0001c0001t0001g0171 others(29): Show |
34 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+1843A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785491 | |||||||
chr5:60785688 | G | C | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+1646C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785688 | |||||||
chr5:60785723 | T | TCATTA | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+1610_64+1611ins others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785723 | |||||||
chr5:60785981 | T | C | 22 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0037 others(19): Show |
24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.64+1353A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60785981 | |||||||
chr5:60786004 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64+1330G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786004 | |||||||
chr5:60786222 | G | A | 11 | a0001c0001t0006g0138 a0001c0001t0006g0140 a0001c0001t0006g0141 others(8): Show |
11 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+1112C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786222 | |||||||
chr5:60786329 | C | T | 1 | a0001c0001t0005g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64+1005G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786329 | |||||||
chr5:60786341 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+993A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786341 | |||||||
chr5:60786390 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0180 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+944G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786390 | |||||||
chr5:60786403 | C | T | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+931G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786403 | |||||||
chr5:60786513 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+821A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786513 | |||||||
chr5:60786718 | G | A | 61 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0152 others(58): Show |
62 | HG00099.hp2 HG00639.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.64+616C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786718 | |||||||
chr5:60786721 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.64+613G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786721 | |||||||
chr5:60786814 | T | C | 147 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0123 others(144): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.64+520A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786814 | |||||||
chr5:60786908 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+426C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786908 | |||||||
chr5:60786923 | C | A | 1 | a0001c0001t0004g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64+411G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786923 | |||||||
chr5:60786975 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+359C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60786975 | |||||||
chr5:60787240 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64+94T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 3/8 | chr5 | 60787240 | |||||||
chr5:60787448 | C | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-34-17G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787448 | |||||||
chr5:60787472 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-41T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787472 | |||||||
chr5:60787675 | A | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | NA18959.hp1 NA18967.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-244T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60787675 | |||||||
chr5:60788076 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-34-645T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788076 | |||||||
chr5:60788193 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-762A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788193 | |||||||
chr5:60788291 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-860A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788291 | |||||||
chr5:60788328 | T | C | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-897A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788328 | |||||||
chr5:60788496 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-34-1065G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788496 | |||||||
chr5:60788522 | C | T | 1 | a0001c0001t0007g0029 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-34-1091G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788522 | |||||||
chr5:60788589 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-34-1158T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788589 | |||||||
chr5:60788664 | AC | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-34-1234delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788664 | |||||||
chr5:60788667 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0054 |
2 | NA18970.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-34-1236G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788667 | |||||||
chr5:60788881 | G | A | 1 | a0001c0001t0023g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-34-1450C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788881 | |||||||
chr5:60788945 | T | C | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-1514A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60788945 | |||||||
chr5:60789066 | A | G | 1 | a0001c0001t0010g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-34-1635T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789066 | |||||||
chr5:60789284 | A | C | 2 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
2 | HG02523.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-34-1853T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789284 | |||||||
chr5:60789413 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-34-1982C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789413 | |||||||
chr5:60789427 | A | T | 1 | a0001c0001t0006g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-34-1996T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789427 | |||||||
chr5:60789662 | A | G | 4 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0028 others(1): Show |
4 | HG01099.hp2 HG01168.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-2231T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789662 | |||||||
chr5:60789802 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-34-2371T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789802 | |||||||
chr5:60789843 | G | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-2412C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789843 | |||||||
chr5:60789909 | G | A | 2 | a0001c0001t0003g0172 a0001c0001t0003g0174 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-34-2478C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789909 | |||||||
chr5:60789936 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-34-2505C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60789936 | |||||||
chr5:60790055 | T | C | 7 | a0001c0001t0001g0171 a0001c0001t0003g0149 a0001c0001t0003g0153 others(4): Show |
7 | HG02258.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-2624A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790055 | |||||||
chr5:60790104 | T | C | 2 | a0001c0001t0001g0085 a0003c0004t0001g0086 |
2 | NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-34-2673A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790104 | |||||||
chr5:60790235 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-34-2804A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790235 | |||||||
chr5:60790248 | G | T | 1 | a0001c0001t0005g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-34-2817C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790248 | |||||||
chr5:60790554 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-34-3123G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790554 | |||||||
chr5:60790571 | T | G | 1 | a0001c0001t0002g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-34-3140A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790571 | |||||||
chr5:60790633 | T | C | 20 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0171 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34-3202A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790633 | |||||||
chr5:60790850 | T | G | 22 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-3419A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790850 | |||||||
chr5:60790909 | A | T | 1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-34-3478T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790909 | |||||||
chr5:60790923 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-3492T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790923 | |||||||
chr5:60790940 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-3509C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790940 | |||||||
chr5:60790983 | G | T | 6 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(3): Show |
6 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-3552C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60790983 | |||||||
chr5:60791073 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(86): Show |
94 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-34-3642G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791073 | |||||||
chr5:60791509 | G | A | 15 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(12): Show |
15 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-4078C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791509 | |||||||
chr5:60791550 | C | A | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-4119G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791550 | |||||||
chr5:60791700 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-4269A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791700 | |||||||
chr5:60791955 | C | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-34-4524G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60791955 | |||||||
chr5:60792123 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-4692C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792123 | |||||||
chr5:60792153 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-4722C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792153 | |||||||
chr5:60792321 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-34-4890T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792321 | |||||||
chr5:60792355 | T | G | 1 | a0001c0001t0003g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-34-4924A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792355 | |||||||
chr5:60792423 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-34-4992G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792423 | |||||||
chr5:60792428 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-34-4997A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792428 | |||||||
chr5:60792792 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-34-5361G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792792 | |||||||
chr5:60792967 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-34-5536T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60792967 | |||||||
chr5:60793265 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-34-5834G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793265 | |||||||
chr5:60793310 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+5870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793310 | |||||||
chr5:60793321 | C | T | 8 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0071 others(5): Show |
8 | HG01109.hp2 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+5859G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793321 | |||||||
chr5:60793442 | G | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+5738C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793442 | |||||||
chr5:60793609 | T | G | 53 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0171 others(50): Show |
54 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-35+5571A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793609 | |||||||
chr5:60793640 | A | C | 3 | a0001c0001t0003g0199 a0001c0001t0011g0200 a0001c0001t0011g0201 |
3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-35+5540T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793640 | |||||||
chr5:60793907 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-35+5273G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793907 | |||||||
chr5:60793952 | G | A | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+5228C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60793952 | |||||||
chr5:60794056 | G | A | 6 | a0001c0001t0003g0151 a0001c0001t0003g0191 a0001c0001t0003g0192 others(3): Show |
6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+5124C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794056 | |||||||
chr5:60794140 | A | C | 6 | a0001c0001t0001g0137 a0001c0001t0006g0138 a0001c0001t0006g0140 others(3): Show |
6 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+5040T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794140 | |||||||
chr5:60794143 | T | G | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35+5037A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794143 | |||||||
chr5:60794183 | T | A | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-35+4997A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794183 | |||||||
chr5:60794224 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-35+4956A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794224 | |||||||
chr5:60794524 | A | T | 2 | a0001c0001t0003g0170 a0001c0001t0003g0173 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-35+4656T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794524 | |||||||
chr5:60794655 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-35+4525C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794655 | |||||||
chr5:60794662 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-35+4518A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794662 | |||||||
chr5:60794674 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-35+4506A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794674 | |||||||
chr5:60794975 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-35+4205G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794975 | |||||||
chr5:60794992 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-35+4188C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60794992 | |||||||
chr5:60795124 | C | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+4056G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795124 | |||||||
chr5:60795219 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3961G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795219 | |||||||
chr5:60795293 | G | C | 1 | a0001c0001t0003g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-35+3887C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795293 | |||||||
chr5:60795325 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0127 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35+3855C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795325 | |||||||
chr5:60795365 | C | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3815G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795365 | |||||||
chr5:60795459 | G | A | 1 | a0001c0001t0004g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-35+3721C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795459 | |||||||
chr5:60795478 | G | C | 1 | a0001c0001t0007g0001 | 3 | HG03490.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-35+3702C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795478 | |||||||
chr5:60795496 | G | A | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-35+3684C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795496 | |||||||
chr5:60795503 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3677A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795503 | |||||||
chr5:60795609 | G | C | 1 | a0001c0001t0007g0033 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-35+3571C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795609 | |||||||
chr5:60795655 | T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-35+3525A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795655 | |||||||
chr5:60795729 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3451T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795729 | |||||||
chr5:60795828 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-35+3352C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795828 | |||||||
chr5:60795846 | AAG | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3332_-35+3333d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795846 | |||||||
chr5:60795853 | G | C | 1 | a0001c0001t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-35+3327C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795853 | |||||||
chr5:60795933 | T | TGCCGCCA others(15): Show |
1 | a0001c0001t0002g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35+3225_-35+3246d others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795933 | |||||||
chr5:60795975 | TAAGAACA | T | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+3198_-35+3204d others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795975 | |||||||
chr5:60795991 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+3189A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795991 | |||||||
chr5:60795995 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35+3185G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60795995 | |||||||
chr5:60796009 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-35+3171A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796009 | |||||||
chr5:60796081 | G | A | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-35+3099C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796081 | |||||||
chr5:60796226 | C | T | 1 | a0001c0001t0003g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-35+2954G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796226 | |||||||
chr5:60796490 | C | T | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+2690G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796490 | |||||||
chr5:60796504 | C | G | 6 | a0001c0001t0003g0151 a0001c0001t0003g0191 a0001c0001t0003g0192 others(3): Show |
6 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2676G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796504 | |||||||
chr5:60796611 | A | G | 1 | a0001c0001t0004g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-35+2569T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796611 | |||||||
chr5:60796623 | C | T | 1 | a0001c0001t0003g0007 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-35+2557G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796623 | |||||||
chr5:60796859 | G | T | 6 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2321C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796859 | |||||||
chr5:60796860 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+2320C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60796860 | |||||||
chr5:60797190 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0092 a0001c0001t0001g0094 others(9): Show |
13 | HG00280.hp1 HG00544.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-35+1990C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797190 | |||||||
chr5:60797268 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-35+1912A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797268 | |||||||
chr5:60797275 | G | A | 2 | a0001c0001t0002g0229 a0001c0001t0002g0232 |
2 | HG00735.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+1905C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797275 | |||||||
chr5:60797560 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+1620G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797560 | |||||||
chr5:60797785 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-35+1395T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797785 | |||||||
chr5:60797939 | C | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+1241G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60797939 | |||||||
chr5:60798063 | T | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+1117A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798063 | |||||||
chr5:60798251 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0004g0055 |
2 | HG02486.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-35+929C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798251 | |||||||
chr5:60798313 | T | C | 17 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0171 others(14): Show |
17 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+867A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798313 | |||||||
chr5:60798345 | C | T | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+835G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798345 | |||||||
chr5:60798350 | T | G | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-35+830A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798350 | |||||||
chr5:60798412 | C | T | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+768G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798412 | |||||||
chr5:60798439 | G | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-35+741C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798439 | |||||||
chr5:60798519 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0074 |
2 | HG02056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-35+661C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60798519 | |||||||
chr5:60799177 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0045 others(51): Show |
56 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.-35+3A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 2/8 | chr5 | 60799177 | |||||||
chr5:60799248 | A | T | 8 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0071 others(5): Show |
8 | HG01109.hp2 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-18T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799248 | |||||||
chr5:60799428 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-85-198G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799428 | |||||||
chr5:60799445 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-215C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799445 | |||||||
chr5:60799502 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-85-272T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799502 | |||||||
chr5:60799514 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-284C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799514 | |||||||
chr5:60799546 | A | T | 4 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0150 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-316T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799546 | |||||||
chr5:60799553 | A | G | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-323T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799553 | |||||||
chr5:60799557 | C | T | 9 | a0001c0001t0005g0010 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-327G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799557 | |||||||
chr5:60799734 | A | G | 2 | a0001c0001t0002g0219 a0001c0001t0002g0220 |
2 | NA18983.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-85-504T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799734 | |||||||
chr5:60799781 | T | C | 13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0082 others(10): Show |
13 | HG00438.hp2 HG02027.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85-551A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799781 | |||||||
chr5:60799841 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-611A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799841 | |||||||
chr5:60799899 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-669A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799899 | |||||||
chr5:60799900 | G | A | 1 | a0001c0001t0002g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-85-670C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799900 | |||||||
chr5:60799908 | A | G | 6 | a0001c0001t0001g0137 a0001c0001t0006g0138 a0001c0001t0006g0140 others(3): Show |
6 | HG02809.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-678T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799908 | |||||||
chr5:60799969 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-739C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799969 | |||||||
chr5:60799993 | C | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0080 a0001c0001t0004g0090 |
4 | NA18612.hp1 NA18945.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-763G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60799993 | |||||||
chr5:60800030 | C | CA | 23 | a0001c0001t0001g0166 a0001c0001t0002g0206 a0001c0001t0002g0207 others(20): Show |
23 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-85-801dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | |||||||
chr5:60800030 | CA | C | 6 | a0001c0001t0002g0234 a0001c0001t0007g0031 a0001c0001t0008g0130 others(3): Show |
6 | HG01496.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-801delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | |||||||
chr5:60800030 | CAAAAAA | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(139): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-85-806_-85-801del others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | |||||||
chr5:60800030 | CAAAAAAA | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0147 a0001c0001t0002g0204 others(4): Show |
7 | HG01884.hp1 HG02132.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-807_-85-801del others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | |||||||
chr5:60800030 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-85-813_-85-801del others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800030 | |||||||
chr5:60800056 | T | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-826A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800056 | |||||||
chr5:60800206 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-976A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800206 | |||||||
chr5:60800400 | G | A | 3 | a0001c0001t0002g0204 a0001c0001t0003g0169 a0001c0001t0008g0203 |
3 | HG01167.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-85-1170C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800400 | |||||||
chr5:60800456 | A | C | 2 | a0001c0001t0002g0210 a0001c0001t0002g0211 |
2 | NA18939.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-85-1226T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800456 | |||||||
chr5:60800670 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-1440A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800670 | |||||||
chr5:60800722 | G | A | 2 | a0001c0001t0012g0241 a0001c0001t0012g0242 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-85-1492C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800722 | |||||||
chr5:60800778 | TC | T | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-1549delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800778 | |||||||
chr5:60800825 | T | G | 1 | a0001c0001t0007g0001 | 3 | HG03490.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-85-1595A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60800825 | |||||||
chr5:60801324 | C | CA | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2095dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801324 | |||||||
chr5:60801333 | A | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(2): Show |
5 | NA18939.hp1 NA18951.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-2103T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801333 | |||||||
chr5:60801444 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-2214C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801444 | |||||||
chr5:60801506 | A | AG | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2277dupC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801506 | |||||||
chr5:60801584 | A | T | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2354T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801584 | |||||||
chr5:60801726 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-85-2496C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801726 | |||||||
chr5:60801731 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-85-2501A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801731 | |||||||
chr5:60801877 | A | T | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2647T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801877 | |||||||
chr5:60801971 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-2741C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60801971 | |||||||
chr5:60802061 | C | CAT | 5 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0005g0011 others(2): Show |
5 | HG00621.hp1 HG00735.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2833_-85-2832d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | C | CATATATA others(3): Show |
1 | a0001c0001t0005g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-85-2841_-85-2832d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CAT | C | 5 | a0001c0001t0001g0137 a0001c0001t0002g0230 a0001c0001t0002g0232 others(2): Show |
5 | HG00738.hp2 HG02602.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-2833_-85-2832d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATAT | C | 6 | a0001c0001t0002g0225 a0001c0001t0006g0140 a0001c0001t0006g0141 others(3): Show |
6 | HG00140.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2835_-85-2832d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATAT | C | 3 | a0001c0001t0006g0138 a0001c0001t0008g0135 a0001c0001t0009g0243 |
3 | HG01981.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-85-2837_-85-2832d others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATATA others(3): Show |
C | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
5 | NA18906.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2841_-85-2832d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATATA others(5): Show |
C | 7 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 others(4): Show |
7 | HG01099.hp1 HG03490.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-2843_-85-2832d others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATATA others(7): Show |
C | 5 | a0001c0001t0002g0224 a0001c0001t0002g0233 a0001c0001t0002g0234 others(2): Show |
5 | HG00639.hp2 HG01261.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-2845_-85-2832d others(16): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0214 |
2 | HG03831.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-85-2847_-85-2832d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802061 | CATATATA others(11): Show |
C | 6 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(3): Show |
6 | HG02135.hp1 NA18939.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2849_-85-2832d others(20): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802061 | |||||||
chr5:60802073 | TATATATA others(41): Show |
T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-2891_-85-2844d others(50): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802073 | |||||||
chr5:60802081 | TATATATA others(37): Show |
T | 48 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0147 others(45): Show |
49 | HG00099.hp2 HG00673.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2852d others(46): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802081 | |||||||
chr5:60802083 | TATATATA others(33): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-85-2893_-85-2854d others(42): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802083 | |||||||
chr5:60802083 | TATATATA others(35): Show |
T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(91): Show |
99 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2854d others(44): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802083 | |||||||
chr5:60802085 | TATATATA others(33): Show |
T | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0006g0072 others(1): Show |
4 | HG02056.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2856d others(42): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802085 | |||||||
chr5:60802087 | TATATATA others(31): Show |
T | 10 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0121 others(7): Show |
10 | HG00639.hp1 HG01167.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-2895_-85-2858d others(40): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802087 | |||||||
chr5:60802089 | TATATATA others(23): Show |
T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2860d others(32): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802089 | |||||||
chr5:60802089 | TATATATA others(29): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-85-2895_-85-2860d others(38): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802089 | |||||||
chr5:60802091 | TATATATA others(27): Show |
T | 1 | a0001c0001t0006g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-2895_-85-2862d others(36): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802091 | |||||||
chr5:60802099 | TATATATA others(13): Show |
T | 1 | a0001c0001t0016g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-2889_-85-2870d others(22): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802099 | |||||||
chr5:60802101 | TATATATA others(11): Show |
T | 5 | a0001c0001t0005g0014 a0001c0001t0007g0001 a0001c0001t0007g0031 others(2): Show |
6 | HG00280.hp2 HG01496.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2872d others(20): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802101 | |||||||
chr5:60802103 | TATATATA others(9): Show |
T | 1 | a0001c0001t0007g0001 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-85-2889_-85-2874d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802103 | |||||||
chr5:60802105 | TATATATA others(7): Show |
T | 6 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0005g0018 others(3): Show |
6 | HG01192.hp2 HG01952.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2889_-85-2876d others(16): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802105 | |||||||
chr5:60802107 | TATATATA others(5): Show |
T | 1 | a0001c0001t0007g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-85-2889_-85-2878d others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802107 | |||||||
chr5:60802109 | TATATATA others(3): Show |
T | 1 | a0001c0001t0005g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-85-2889_-85-2880d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802109 | |||||||
chr5:60802113 | T | C | 1 | a0001c0001t0008g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-2883A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802113 | |||||||
chr5:60802115 | T | C | 4 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0008g0132 others(1): Show |
4 | HG02622.hp1 NA18939.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2885A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802115 | |||||||
chr5:60802115 | TATAC | T | 3 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0024 |
3 | HG01069.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-85-2889_-85-2886d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802115 | |||||||
chr5:60802117 | T | C | 20 | a0001c0001t0001g0137 a0001c0001t0002g0206 a0001c0001t0002g0209 others(17): Show |
20 | HG02135.hp1 HG02622.hp1 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.-85-2887A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802117 | |||||||
chr5:60802117 | TAC | T | 3 | a0001c0001t0005g0015 a0001c0001t0005g0023 a0001c0001t0015g0022 |
3 | HG00738.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-85-2889_-85-2888d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802117 | |||||||
chr5:60802119 | C | T | 11 | a0001c0001t0001g0166 a0001c0001t0005g0010 a0001c0001t0005g0011 others(8): Show |
11 | HG00140.hp1 HG01099.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2889G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802119 | |||||||
chr5:60802123 | C | T | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-2893G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802123 | |||||||
chr5:60802257 | T | C | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85-3027A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802257 | |||||||
chr5:60802419 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-85-3189A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802419 | |||||||
chr5:60802440 | A | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-85-3210T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802440 | |||||||
chr5:60802748 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-85-3518T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802748 | |||||||
chr5:60802962 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-3732G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60802962 | |||||||
chr5:60803034 | C | T | 13 | a0001c0001t0001g0137 a0001c0001t0006g0138 a0001c0001t0006g0140 others(10): Show |
13 | HG02622.hp1 HG02647.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-3804G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803034 | |||||||
chr5:60803467 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-85-4237G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803467 | |||||||
chr5:60803468 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-85-4238C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803468 | |||||||
chr5:60803631 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0008g0203 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-85-4401C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803631 | |||||||
chr5:60803904 | A | T | 2 | a0001c0001t0005g0013 a0001c0001t0005g0014 |
2 | NA20300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-85-4674T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803904 | |||||||
chr5:60803976 | T | C | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-4746A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60803976 | |||||||
chr5:60804083 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0002g0231 |
2 | HG00621.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-85-4853A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804083 | |||||||
chr5:60804562 | A | G | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-5332T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804562 | |||||||
chr5:60804617 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0180 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-85-5387G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60804617 | |||||||
chr5:60805036 | A | G | 2 | a0001c0001t0003g0186 a0001c0001t0003g0189 |
2 | HG00673.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-85-5806T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805036 | |||||||
chr5:60805110 | C | T | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85-5880G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805110 | |||||||
chr5:60805282 | C | A | 1 | a0001c0001t0002g0184 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-85-6052G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805282 | |||||||
chr5:60805426 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-6196C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805426 | |||||||
chr5:60805465 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-85-6235T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805465 | |||||||
chr5:60805470 | G | A | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-6240C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805470 | |||||||
chr5:60805490 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-85-6260A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805490 | |||||||
chr5:60805862 | T | C | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-6632A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60805862 | |||||||
chr5:60806488 | C | G | 2 | a0001c0001t0003g0193 a0001c0001t0003g0195 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-85-7258G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806488 | |||||||
chr5:60806607 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-85-7377A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806607 | |||||||
chr5:60806717 | C | T | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-7487G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806717 | |||||||
chr5:60806903 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-7673T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806903 | |||||||
chr5:60806994 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-85-7764C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60806994 | |||||||
chr5:60807095 | A | G | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG02523.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-85-7865T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807095 | |||||||
chr5:60807107 | G | T | 7 | a0001c0001t0001g0129 a0001c0001t0006g0143 a0001c0001t0006g0163 others(4): Show |
7 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-7877C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807107 | |||||||
chr5:60807266 | A | T | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG02523.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-85-8036T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807266 | |||||||
chr5:60807530 | G | GA | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-85-8301dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807530 | |||||||
chr5:60807625 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-8395G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807625 | |||||||
chr5:60807665 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-85-8435T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807665 | |||||||
chr5:60807726 | G | A | 2 | a0001c0001t0009g0243 a0001c0001t0009g0250 |
2 | HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-85-8496C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807726 | |||||||
chr5:60807727 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-8497G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807727 | |||||||
chr5:60807737 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-8507G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807737 | |||||||
chr5:60807770 | C | A | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-8540G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807770 | |||||||
chr5:60807771 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-85-8541T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807771 | |||||||
chr5:60807826 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-85-8596G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807826 | |||||||
chr5:60807827 | G | A | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-8597C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807827 | |||||||
chr5:60807843 | CA | C | 22 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 others(19): Show |
22 | HG00621.hp1 HG00639.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-85-8614delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807843 | |||||||
chr5:60807988 | G | A | 1 | a0001c0001t0004g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-85-8758C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807988 | |||||||
chr5:60807992 | C | A | 1 | a0001c0001t0004g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-85-8762G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60807992 | C | CA | 41 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0165 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.-85-8763dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60807992 | C | CAA | 12 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0220 others(9): Show |
12 | HG00621.hp1 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-8764_-85-8763d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60807992 | CA | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(117): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-85-8763delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60807992 | CAA | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0108 others(6): Show |
9 | HG01168.hp2 HG01175.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-8764_-85-8763d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60807992 | CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-8778_-85-8763d others(18): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60807992 | |||||||
chr5:60808330 | T | C | 7 | a0001c0001t0001g0129 a0001c0001t0006g0143 a0001c0001t0006g0163 others(4): Show |
7 | HG01175.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-9100A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808330 | |||||||
chr5:60808408 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-9178T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808408 | |||||||
chr5:60808533 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-9303A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808533 | |||||||
chr5:60808675 | G | GT | 4 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-9446dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808675 | |||||||
chr5:60808763 | A | G | 1 | a0001c0001t0005g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-85-9533T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60808763 | |||||||
chr5:60809275 | A | T | 1 | a0001c0001t0004g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-85-10045T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809275 | |||||||
chr5:60809409 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-10179A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809409 | |||||||
chr5:60809673 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0121 |
2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-85-10443C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809673 | |||||||
chr5:60809708 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-10478G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809708 | |||||||
chr5:60809798 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-85-10568C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809798 | |||||||
chr5:60809800 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-85-10570G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60809800 | |||||||
chr5:60810179 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-10949C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810179 | |||||||
chr5:60810237 | T | C | 3 | a0001c0001t0003g0199 a0001c0001t0011g0200 a0001c0001t0011g0201 |
3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-85-11007A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810237 | |||||||
chr5:60810420 | C | T | 2 | a0001c0001t0003g0160 a0001c0001t0003g0164 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-85-11190G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810420 | |||||||
chr5:60810656 | G | A | 1 | a0001c0001t0012g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-85-11426C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810656 | |||||||
chr5:60810736 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-85-11506A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810736 | |||||||
chr5:60810784 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-85-11554C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60810784 | |||||||
chr5:60811175 | TA | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-11946delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811175 | |||||||
chr5:60811182 | A | C | 1 | a0001c0001t0005g0010 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-85-11952T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811182 | |||||||
chr5:60811236 | G | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-12006C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811236 | |||||||
chr5:60811283 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-85-12053A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811283 | |||||||
chr5:60811463 | A | G | 1 | a0001c0001t0006g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-12233T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811463 | |||||||
chr5:60811858 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-85-12628T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60811858 | |||||||
chr5:60812230 | T | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-13000A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812230 | |||||||
chr5:60812338 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-13108T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812338 | |||||||
chr5:60812388 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0105 others(4): Show |
7 | HG00408.hp1 NA18970.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-13158A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812388 | |||||||
chr5:60812443 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0106 a0001c0001t0001g0119 |
3 | NA19004.hp1 NA19074.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-85-13213C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812443 | |||||||
chr5:60812643 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-85-13413A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812643 | |||||||
chr5:60812703 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0202 a0001c0001t0023g0162 |
3 | HG01175.hp2 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-85-13473A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812703 | |||||||
chr5:60812724 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-13494C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812724 | |||||||
chr5:60812844 | G | C | 55 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0001g0171 others(52): Show |
56 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-85-13614C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812844 | |||||||
chr5:60812884 | G | A | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-13654C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812884 | |||||||
chr5:60812923 | T | G | 1 | a0001c0003t0006g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-85-13693A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60812923 | |||||||
chr5:60813097 | C | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-13867G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813097 | |||||||
chr5:60813134 | A | G | 22 | a0001c0001t0001g0099 a0001c0001t0004g0005 a0001c0001t0004g0006 others(19): Show |
24 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-85-13904T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813134 | |||||||
chr5:60813230 | T | C | 1 | a0001c0001t0006g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-85-14000A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813230 | |||||||
chr5:60813324 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-85-14094G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813324 | |||||||
chr5:60813620 | C | G | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-14390G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813620 | |||||||
chr5:60813695 | T | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-14465A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813695 | |||||||
chr5:60813775 | A | T | 1 | a0001c0001t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-85-14545T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813775 | |||||||
chr5:60813780 | G | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-85-14550C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60813780 | |||||||
chr5:60814057 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-14827G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814057 | |||||||
chr5:60814378 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-85-15148A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814378 | |||||||
chr5:60814382 | A | G | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-15152T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814382 | |||||||
chr5:60814649 | A | C | 2 | a0001c0001t0001g0129 a0001c0001t0020g0128 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-85-15419T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814649 | |||||||
chr5:60814782 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-85-15552C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814782 | |||||||
chr5:60814785 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-85-15555C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60814785 | |||||||
chr5:60815014 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-85-15784T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815014 | |||||||
chr5:60815477 | C | G | 1 | a0001c0001t0006g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-85-16247G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815477 | |||||||
chr5:60815535 | C | CAATAAAA others(19): Show |
1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-16331_-85-1630 others(30): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815535 | |||||||
chr5:60815535 | CAATAAAA others(19): Show |
C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-85-16331_-85-1630 others(30): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815535 | |||||||
chr5:60815551 | TTTTATAA others(18): Show |
T | 1 | a0001c0001t0012g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-85-16346_-85-1632 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815551 | |||||||
chr5:60815661 | G | A | 1 | a0001c0001t0023g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-85-16431C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815661 | |||||||
chr5:60815716 | C | T | 2 | a0001c0001t0006g0072 a0001c0001t0006g0073 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-85-16486G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815716 | |||||||
chr5:60815752 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0045 others(52): Show |
57 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-85-16522T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815752 | |||||||
chr5:60815826 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-85-16596A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815826 | |||||||
chr5:60815983 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-85-16753A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60815983 | |||||||
chr5:60816083 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-16853T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816083 | |||||||
chr5:60816088 | T | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0168 a0001c0001t0003g0172 others(1): Show |
5 | HG00099.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-16858A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816088 | |||||||
chr5:60816122 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-85-16892T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816122 | |||||||
chr5:60816176 | T | C | 1 | a0001c0001t0006g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-85-16946A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816176 | |||||||
chr5:60816209 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-85-16979T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816209 | |||||||
chr5:60816380 | C | CA | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-17151dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816380 | |||||||
chr5:60816380 | CA | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-17151delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816380 | |||||||
chr5:60816610 | T | C | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-17380A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816610 | |||||||
chr5:60816652 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-85-17422C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60816652 | |||||||
chr5:60817679 | C | CACACACA others(10): Show |
97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(94): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-85-18466_-85-1845 others(21): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817679 | |||||||
chr5:60817679 | CACACACA others(10): Show |
C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-18466_-85-1845 others(21): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817679 | |||||||
chr5:60817810 | A | G | 3 | a0001c0001t0004g0006 a0001c0001t0004g0080 a0001c0001t0004g0090 |
4 | NA18612.hp1 NA18945.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-18580T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817810 | |||||||
chr5:60817822 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-85-18592C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817822 | |||||||
chr5:60817824 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-18594T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817824 | |||||||
chr5:60817830 | A | ATG | 6 | a0001c0001t0001g0129 a0001c0001t0002g0002 a0001c0001t0002g0187 others(3): Show |
7 | HG02056.hp2 HG02630.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-18602_-85-1860 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817830 | |||||||
chr5:60817842 | GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-18620_-85-1861 others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817842 | |||||||
chr5:60817848 | GTA | G | 10 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-18620_-85-1861 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817848 | |||||||
chr5:60817850 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-85-18620T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817850 | |||||||
chr5:60817852 | A | G | 20 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(17): Show |
21 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-18622T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60817852 | |||||||
chr5:60818319 | G | GA | 25 | a0001c0001t0001g0094 a0001c0001t0001g0137 a0001c0001t0001g0165 others(22): Show |
25 | HG00438.hp2 HG01175.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-85-19090dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | |||||||
chr5:60818319 | GA | G | 79 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0062 others(76): Show |
80 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-85-19090delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | |||||||
chr5:60818319 | GAA | G | 40 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(37): Show |
42 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-85-19091_-85-1909 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818319 | |||||||
chr5:60818408 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-19178A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818408 | |||||||
chr5:60818433 | A | T | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-85-19203T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60818433 | |||||||
chr5:60819015 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-19785T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819015 | |||||||
chr5:60819020 | A | AGAGGGGA others(8): Show |
3 | a0001c0001t0010g0245 a0001c0001t0010g0246 a0001c0001t0010g0247 |
3 | HG00140.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-85-19805_-85-1979 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819020 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-19790T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819020 | AGAGGG | A | 6 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0006g0141 others(3): Show |
6 | HG00621.hp1 HG01261.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-19795_-85-1979 others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819020 | AGAGGGGA others(3): Show |
A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0205 a0001c0001t0002g0206 others(11): Show |
14 | HG02135.hp1 HG02809.hp1 HG03225.hp1 others(11): Show |
intron_variant | MODIFIER | c.-85-19800_-85-1979 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819020 | AGAGGGGA others(8): Show |
A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0214 |
2 | HG03831.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-85-19805_-85-1979 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819020 | AGAGGGGA others(13): Show |
A | 1 | a0001c0001t0009g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-85-19810_-85-1979 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819020 | |||||||
chr5:60819023 | G | C | 1 | a0001c0001t0002g0002 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-85-19793C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819023 | |||||||
chr5:60819031 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19801C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819031 | |||||||
chr5:60819032 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19802T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819032 | |||||||
chr5:60819044 | GGGAGGGG others(83): Show |
G | 1 | a0001c0001t0019g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-85-19904_-85-1981 others(94): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819044 | |||||||
chr5:60819054 | GGGAGGGG others(63): Show |
G | 1 | a0001c0001t0001g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-85-19894_-85-1982 others(74): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819054 | |||||||
chr5:60819055 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-85-19825C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819055 | |||||||
chr5:60819059 | GGGAGGGG others(38): Show |
G | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-19874_-85-1983 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | |||||||
chr5:60819059 | GGGAGGGG others(48): Show |
G | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1983 others(59): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | |||||||
chr5:60819059 | GGGAGGGG others(58): Show |
G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-19894_-85-1983 others(69): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | |||||||
chr5:60819059 | GGGAGGGG others(68): Show |
G | 2 | a0001c0001t0003g0071 a0001c0001t0006g0073 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-85-19904_-85-1983 others(79): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819059 | |||||||
chr5:60819064 | GGGAGGGG others(43): Show |
G | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1983 others(54): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819064 | |||||||
chr5:60819064 | GGGAGGGG others(63): Show |
G | 22 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0094 others(19): Show |
22 | HG00099.hp1 HG01358.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1983 others(74): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819064 | |||||||
chr5:60819069 | GGGAGGGG others(28): Show |
G | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-19874_-85-1984 others(39): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | |||||||
chr5:60819069 | GGGAGGGG others(38): Show |
G | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-85-19884_-85-1984 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | |||||||
chr5:60819069 | GGGAGGGG others(58): Show |
G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0042 others(40): Show |
46 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1984 others(69): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819069 | |||||||
chr5:60819070 | GGAGGGGA others(55): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-85-19902_-85-1984 others(66): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819070 | |||||||
chr5:60819074 | GGGAGGGG others(53): Show |
G | 29 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0083 others(26): Show |
29 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1984 others(64): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819074 | |||||||
chr5:60819079 | GGGAGGGG others(48): Show |
G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0048 others(35): Show |
39 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1985 others(59): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819079 | |||||||
chr5:60819084 | GGGAGGGG others(43): Show |
G | 26 | a0001c0001t0001g0003 a0001c0001t0002g0068 a0001c0001t0003g0113 others(23): Show |
27 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1985 others(54): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819084 | |||||||
chr5:60819085 | GGAGGGGA others(40): Show |
G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19902_-85-1985 others(51): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819085 | |||||||
chr5:60819089 | GGGAGGGG others(13): Show |
G | 1 | a0001c0001t0008g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-19879_-85-1986 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819089 | |||||||
chr5:60819089 | GGGAGGGG others(38): Show |
G | 12 | a0001c0001t0001g0104 a0001c0001t0005g0011 a0001c0001t0005g0015 others(9): Show |
14 | HG00738.hp1 HG01069.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1986 others(49): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819089 | |||||||
chr5:60819094 | G | A | 6 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 others(3): Show |
6 | HG00621.hp1 HG03490.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-19864C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | |||||||
chr5:60819094 | G | GGGAGA | 3 | a0001c0001t0002g0223 a0001c0001t0002g0225 a0001c0001t0002g0229 |
3 | HG00735.hp2 HG01099.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-85-19865_-85-1986 others(9): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | |||||||
chr5:60819094 | GGGAGGGG others(33): Show |
G | 5 | a0001c0001t0005g0020 a0001c0001t0007g0031 a0001c0001t0007g0034 others(2): Show |
5 | HG01192.hp2 HG01358.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-19904_-85-1986 others(44): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819094 | |||||||
chr5:60819099 | G | A | 18 | a0001c0001t0001g0137 a0001c0001t0002g0205 a0001c0001t0002g0207 others(15): Show |
18 | HG00621.hp1 HG00735.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-19869C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGAGG others(3): Show |
5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
5 | HG03471.hp2 NA18983.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-19879_-85-1987 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGAGG others(8): Show |
1 | a0001c0001t0002g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-85-19884_-85-1987 others(19): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGGGG others(3): Show |
3 | a0001c0001t0002g0222 a0001c0001t0002g0224 a0001c0001t0002g0240 |
3 | HG00639.hp2 HG01952.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-85-19870_-85-1986 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGGGG others(13): Show |
2 | a0001c0001t0002g0228 a0001c0001t0024g0215 |
2 | HG04204.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-85-19870_-85-1986 others(24): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGGGG others(18): Show |
1 | a0001c0001t0002g0233 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-85-19870_-85-1986 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | G | GGGAGGGG others(18): Show |
1 | a0001c0001t0002g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-85-19870_-85-1986 others(29): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | GGGAGAGG others(3): Show |
G | 5 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0134 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-19879_-85-1987 others(14): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | GGGAGAGG others(23): Show |
G | 2 | a0001c0001t0007g0032 a0001c0001t0017g0035 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-85-19899_-85-1987 others(34): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819099 | GGGAGAGG others(28): Show |
G | 1 | a0001c0001t0007g0033 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-85-19904_-85-1987 others(39): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819099 | |||||||
chr5:60819109 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19879T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819109 | |||||||
chr5:60819114 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19884T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819114 | |||||||
chr5:60819119 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19889T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819119 | |||||||
chr5:60819124 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19894T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819124 | |||||||
chr5:60819129 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-85-19899T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819129 | |||||||
chr5:60819133 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-19903C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819133 | |||||||
chr5:60819134 | A | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0166 a0001c0001t0007g0032 others(1): Show |
4 | HG01361.hp1 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-19904T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819134 | |||||||
chr5:60819252 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-85-20022T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819252 | |||||||
chr5:60819374 | G | A | 4 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-20144C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819374 | |||||||
chr5:60819546 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-85-20316G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819546 | |||||||
chr5:60819601 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-20371C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819601 | |||||||
chr5:60819639 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-85-20409G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819639 | |||||||
chr5:60819690 | G | T | 1 | a0001c0001t0016g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-20460C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819690 | |||||||
chr5:60819840 | G | A | 2 | a0001c0001t0005g0016 a0001c0001t0005g0023 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-85-20610C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60819840 | |||||||
chr5:60820170 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-85-20940C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820170 | |||||||
chr5:60820260 | T | C | 2 | a0001c0001t0006g0140 a0001c0003t0006g0139 |
2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-85-21030A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820260 | |||||||
chr5:60820330 | C | A | 2 | a0001c0001t0008g0135 a0001c0001t0008g0136 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-85-21100G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820330 | |||||||
chr5:60820369 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0165 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-21139A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820369 | |||||||
chr5:60820586 | C | T | 1 | a0001c0001t0016g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-21356G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820586 | |||||||
chr5:60820706 | C | T | 24 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 others(21): Show |
24 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-85-21476G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820706 | |||||||
chr5:60820786 | T | C | 8 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(5): Show |
10 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85-21556A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820786 | |||||||
chr5:60820923 | A | G | 1 | a0001c0001t0016g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-85-21693T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60820923 | |||||||
chr5:60821053 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(180): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-85-21823G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821053 | |||||||
chr5:60821057 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-85-21827G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821057 | |||||||
chr5:60821282 | T | G | 1 | a0001c0001t0004g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-85-22052A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821282 | |||||||
chr5:60821375 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-85-22145T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821375 | |||||||
chr5:60821375 | A | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-22145T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821375 | |||||||
chr5:60821654 | T | C | 2 | a0001c0001t0012g0241 a0001c0001t0012g0242 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-85-22424A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821654 | |||||||
chr5:60821679 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-85-22449T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821679 | |||||||
chr5:60821711 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-86+22449A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821711 | |||||||
chr5:60821896 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-86+22264A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60821896 | |||||||
chr5:60822163 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-86+21997A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822163 | |||||||
chr5:60822284 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-86+21876C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822284 | |||||||
chr5:60822488 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-86+21672T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822488 | |||||||
chr5:60822936 | C | T | 1 | a0001c0001t0024g0215 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-86+21224G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60822936 | |||||||
chr5:60823010 | A | G | 1 | a0001c0001t0019g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-86+21150T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823010 | |||||||
chr5:60823045 | G | A | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+21115C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823045 | |||||||
chr5:60823058 | GAGA | G | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+21099_-86+2110 others(7): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823058 | |||||||
chr5:60823134 | T | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-86+21026A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823134 | |||||||
chr5:60823135 | GAAGT | G | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+21021_-86+2102 others(8): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823135 | |||||||
chr5:60823205 | A | C | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+20955T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823205 | |||||||
chr5:60823270 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-86+20890G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823270 | |||||||
chr5:60823271 | G | A | 6 | a0001c0001t0001g0067 a0001c0001t0006g0143 a0001c0001t0006g0163 others(3): Show |
6 | HG00099.hp1 HG01175.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+20889C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823271 | |||||||
chr5:60823360 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-86+20800C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823360 | |||||||
chr5:60823838 | G | A | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+20322C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823838 | |||||||
chr5:60823897 | G | C | 1 | a0001c0001t0004g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-86+20263C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823897 | |||||||
chr5:60823910 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(149): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-86+20250T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60823910 | |||||||
chr5:60824072 | A | T | 2 | a0001c0001t0003g0172 a0001c0001t0003g0174 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-86+20088T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824072 | |||||||
chr5:60824295 | C | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(188): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-86+19865G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824295 | |||||||
chr5:60824362 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0008g0203 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+19798C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824362 | |||||||
chr5:60824384 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-86+19776C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824384 | |||||||
chr5:60824456 | A | G | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+19704T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824456 | |||||||
chr5:60824867 | T | A | 1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+19293A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824867 | |||||||
chr5:60824894 | C | A | 1 | a0001c0001t0004g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-86+19266G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824894 | |||||||
chr5:60824963 | T | TC | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+19196_-86+1919 others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60824963 | |||||||
chr5:60825171 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+18989C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825171 | |||||||
chr5:60825270 | A | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(207): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-86+18890T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825270 | |||||||
chr5:60825411 | C | T | 31 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-86+18749G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825411 | |||||||
chr5:60825444 | T | C | 36 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(33): Show |
38 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-86+18716A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825444 | |||||||
chr5:60825482 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+18678G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825482 | |||||||
chr5:60825535 | G | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(194): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-86+18625C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825535 | |||||||
chr5:60825643 | A | T | 8 | a0001c0001t0007g0001 a0001c0001t0007g0031 a0001c0001t0007g0032 others(5): Show |
10 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-86+18517T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825643 | |||||||
chr5:60825647 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+18513C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60825647 | |||||||
chr5:60826372 | A | AT | 5 | a0001c0001t0006g0143 a0001c0001t0006g0163 a0001c0001t0006g0202 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+17787dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826372 | |||||||
chr5:60826374 | T | A | 30 | a0001c0001t0001g0166 a0001c0001t0005g0008 a0001c0001t0005g0010 others(27): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+17786A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826374 | |||||||
chr5:60826557 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0019g0041 |
2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-86+17603C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826557 | |||||||
chr5:60826564 | C | T | 1 | a0002c0002t0002g0110 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-86+17596G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826564 | |||||||
chr5:60826580 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-86+17580A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826580 | |||||||
chr5:60826809 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+17351G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60826809 | |||||||
chr5:60827047 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-86+17113T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827047 | |||||||
chr5:60827077 | C | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0012g0241 others(2): Show |
5 | HG01192.hp1 HG01433.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+17083G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827077 | |||||||
chr5:60827156 | C | T | 1 | a0001c0001t0017g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-86+17004G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827156 | |||||||
chr5:60827236 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-86+16924G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827236 | |||||||
chr5:60827454 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG01099.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-86+16706T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827454 | |||||||
chr5:60827934 | C | T | 1 | a0001c0001t0024g0215 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-86+16226G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827934 | |||||||
chr5:60827956 | G | A | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+16204C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827956 | |||||||
chr5:60827961 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-86+16199T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60827961 | |||||||
chr5:60828013 | AC | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.-86+16146delG | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828013 | |||||||
chr5:60828096 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+16064A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828096 | |||||||
chr5:60828178 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-86+15982G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828178 | |||||||
chr5:60828331 | C | CTA | 3 | a0001c0001t0006g0163 a0001c0001t0006g0202 a0001c0001t0023g0162 |
3 | HG01175.hp2 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-86+15828_-86+1582 others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828331 | |||||||
chr5:60828406 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-86+15754A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828406 | |||||||
chr5:60828453 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-86+15707A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828453 | |||||||
chr5:60828644 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+15516C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60828644 | |||||||
chr5:60829014 | A | G | 1 | a0001c0001t0013g0009 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-86+15146T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829014 | |||||||
chr5:60829110 | T | A | 1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+15050A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829110 | |||||||
chr5:60829168 | C | CA | 30 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(27): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+14991dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829168 | |||||||
chr5:60829199 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+14961C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829199 | |||||||
chr5:60829203 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0068 |
2 | NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-86+14957G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829203 | |||||||
chr5:60829277 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0165 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+14883C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829277 | |||||||
chr5:60829401 | T | G | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+14759A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829401 | |||||||
chr5:60829463 | A | G | 1 | a0001c0001t0003g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-86+14697T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829463 | |||||||
chr5:60829525 | T | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+14635A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829525 | |||||||
chr5:60829615 | T | C | 1 | a0001c0001t0006g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-86+14545A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60829615 | |||||||
chr5:60830045 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+14115G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830045 | |||||||
chr5:60830439 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-86+13721A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830439 | |||||||
chr5:60830475 | A | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
12 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+13685T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830475 | |||||||
chr5:60830597 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(181): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-86+13563A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830597 | |||||||
chr5:60830609 | CT | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0092 a0001c0001t0001g0093 others(9): Show |
13 | HG00280.hp1 HG00544.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+13550delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830609 | |||||||
chr5:60830613 | T | C | 11 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG00621.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+13547A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60830613 | |||||||
chr5:60831232 | G | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+12928C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831232 | |||||||
chr5:60831468 | A | G | 3 | a0001c0001t0003g0178 a0001c0001t0003g0179 a0001c0001t0003g0180 |
3 | HG01516.hp1 HG01517.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-86+12692T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831468 | |||||||
chr5:60831690 | A | T | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+12470T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831690 | |||||||
chr5:60831842 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-86+12318G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831842 | |||||||
chr5:60831897 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(94): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-86+12263A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831897 | |||||||
chr5:60831976 | A | C | 1 | a0001c0001t0002g0221 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-86+12184T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60831976 | |||||||
chr5:60832366 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0121 |
3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-86+11794A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832366 | |||||||
chr5:60832370 | T | G | 3 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-86+11790A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832370 | |||||||
chr5:60832652 | T | A | 1 | a0001c0001t0004g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-86+11508A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832652 | |||||||
chr5:60832659 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-86+11501G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832659 | |||||||
chr5:60832662 | C | T | 17 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(14): Show |
17 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-86+11498G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832662 | |||||||
chr5:60832813 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-86+11347C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60832813 | |||||||
chr5:60833069 | A | C | 1 | a0001c0001t0003g0174 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-86+11091T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833069 | |||||||
chr5:60833186 | T | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG01069.hp2 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+10974A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833186 | |||||||
chr5:60833501 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+10659C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833501 | |||||||
chr5:60833534 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-86+10626T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833534 | |||||||
chr5:60833594 | A | G | 1 | a0002c0002t0001g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-86+10566T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833594 | |||||||
chr5:60833845 | T | C | 1 | a0001c0001t0006g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-86+10315A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833845 | |||||||
chr5:60833868 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-86+10292A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833868 | |||||||
chr5:60833921 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0059 others(1): Show |
5 | HG00438.hp1 HG00673.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+10239T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833921 | |||||||
chr5:60833956 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-86+10204T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60833956 | |||||||
chr5:60834391 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-86+9769G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834391 | |||||||
chr5:60834540 | C | T | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+9620G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834540 | |||||||
chr5:60834684 | A | C | 1 | a0001c0001t0002g0002 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-86+9476T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834684 | |||||||
chr5:60834730 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-86+9430G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834730 | |||||||
chr5:60834775 | G | A | 1 | a0001c0001t0008g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-86+9385C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834775 | |||||||
chr5:60834781 | GT | G | 3 | a0001c0001t0005g0021 a0001c0001t0005g0024 a0001c0001t0015g0022 |
3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+9378delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834781 | |||||||
chr5:60834786 | TTGATTTT others(2459): Show |
T | 3 | a0001c0001t0005g0021 a0001c0001t0005g0024 a0001c0001t0015g0022 |
3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+6908_-86+9373d others(2): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60834786 | |||||||
chr5:60835008 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(241): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-86+9152G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835008 | |||||||
chr5:60835020 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+9140C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835020 | |||||||
chr5:60835156 | C | T | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+9004G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835156 | |||||||
chr5:60835190 | G | GA | 17 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00438.hp2 HG01109.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-86+8969dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835190 | |||||||
chr5:60835190 | GA | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0197 a0001c0001t0002g0211 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+8969delT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835190 | |||||||
chr5:60835467 | A | G | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8693T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835467 | |||||||
chr5:60835570 | C | A | 1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+8590G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835570 | |||||||
chr5:60835824 | C | T | 27 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
29 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-86+8336G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835824 | |||||||
chr5:60835930 | C | G | 1 | a0001c0001t0005g0017 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-86+8230G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835930 | |||||||
chr5:60835989 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-86+8171G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60835989 | |||||||
chr5:60836016 | G | A | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8144C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836016 | |||||||
chr5:60836057 | T | C | 27 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(24): Show |
29 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-86+8103A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836057 | |||||||
chr5:60836119 | A | C | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8041T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836119 | |||||||
chr5:60836142 | C | CAT | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(100): Show |
108 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-86+8016_-86+8017d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836142 | |||||||
chr5:60836285 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-86+7875C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836285 | |||||||
chr5:60836358 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+7802A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60836358 | |||||||
chr5:60837253 | T | A | 3 | a0001c0001t0005g0021 a0001c0001t0005g0024 a0001c0001t0015g0022 |
3 | HG02145.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-86+6907A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837253 | |||||||
chr5:60837290 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-86+6870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837290 | |||||||
chr5:60837297 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-86+6863G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837297 | |||||||
chr5:60837313 | GGTGGGGG others(4): Show |
G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+6836_-86+6846d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837313 | |||||||
chr5:60837314 | GTGGGGGG others(3): Show |
G | 1 | a0001c0001t0005g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-86+6836_-86+6845d others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837314 | |||||||
chr5:60837315 | T | G | 11 | a0001c0001t0001g0045 a0001c0001t0001g0109 a0001c0001t0001g0165 others(8): Show |
11 | HG00621.hp2 HG01261.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+6845A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837315 | T | TG | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0059 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-86+6844dupC | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837315 | T | TGG | 36 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(33): Show |
39 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-86+6843_-86+6844d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837315 | T | TGGG | 16 | a0001c0001t0001g0107 a0001c0001t0001g0126 a0001c0001t0001g0147 others(13): Show |
16 | HG01109.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-86+6842_-86+6844d others(5): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837315 | T | TGGGG | 15 | a0001c0001t0001g0108 a0001c0001t0003g0153 a0001c0001t0003g0154 others(12): Show |
15 | HG01109.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-86+6841_-86+6844d others(6): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837315 | T | TGGGGGGG others(4): Show |
1 | a0001c0001t0003g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-86+6844_-86+6845i others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837315 | |||||||
chr5:60837322 | GGAGTGGG others(4): Show |
G | 1 | a0001c0001t0020g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-86+6827_-86+6837d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837322 | |||||||
chr5:60837324 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(196): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-86+6836T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837324 | |||||||
chr5:60837324 | A | T | 1 | a0001c0001t0003g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-86+6836T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837324 | |||||||
chr5:60837325 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0009g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-86+6834_-86+6835i others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837325 | |||||||
chr5:60837326 | T | G | 13 | a0001c0001t0001g0048 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
13 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+6834A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837326 | |||||||
chr5:60837332 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-86+6827_-86+6828i others(12): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837332 | |||||||
chr5:60837333 | T | C | 2 | a0001c0001t0002g0204 a0001c0001t0008g0203 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+6827A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837333 | |||||||
chr5:60837333 | T | G | 11 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0003g0007 others(8): Show |
12 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+6827A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837333 | |||||||
chr5:60837465 | G | A | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-86+6695C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837465 | |||||||
chr5:60837866 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0008g0203 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-86+6294G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837866 | |||||||
chr5:60837880 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(182): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-86+6280T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60837880 | |||||||
chr5:60838290 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-86+5870C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838290 | |||||||
chr5:60838462 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-86+5698T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838462 | |||||||
chr5:60838513 | G | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+5647C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838513 | |||||||
chr5:60838541 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5619G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838541 | |||||||
chr5:60838550 | A | C | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+5610T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838550 | |||||||
chr5:60838811 | G | A | 18 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0002g0181 others(15): Show |
18 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.-86+5349C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838811 | |||||||
chr5:60838852 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0004g0047 |
2 | HG02818.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-86+5308G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838852 | |||||||
chr5:60838950 | G | A | 6 | a0001c0001t0001g0171 a0001c0001t0003g0191 a0001c0001t0003g0192 others(3): Show |
6 | HG02145.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5210C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60838950 | |||||||
chr5:60839021 | CAA | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(160): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.-86+5137_-86+5138d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839021 | |||||||
chr5:60839027 | A | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0168 |
2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-86+5133T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839027 | |||||||
chr5:60839029 | A | T | 51 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0197 others(48): Show |
52 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.-86+5131T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839029 | |||||||
chr5:60839031 | T | A | 12 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0164 others(9): Show |
12 | HG01175.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+5129A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839031 | |||||||
chr5:60839033 | T | A | 5 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+5127A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839033 | |||||||
chr5:60839044 | A | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+5116T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839044 | |||||||
chr5:60839294 | G | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(238): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-86+4866C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839294 | |||||||
chr5:60839355 | G | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+4805C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839355 | |||||||
chr5:60839685 | G | A | 1 | a0001c0001t0004g0116 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-86+4475C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60839685 | |||||||
chr5:60840037 | G | A | 1 | a0001c0001t0006g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-86+4123C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840037 | |||||||
chr5:60840132 | G | C | 2 | a0001c0001t0008g0135 a0001c0001t0008g0136 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-86+4028C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840132 | |||||||
chr5:60840135 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(87): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+4025C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840135 | |||||||
chr5:60840158 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(165): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-86+4002T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840158 | |||||||
chr5:60840286 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-86+3874A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840286 | |||||||
chr5:60840627 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(87): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+3533G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840627 | |||||||
chr5:60840700 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0165 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+3460G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840700 | |||||||
chr5:60840741 | A | T | 19 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0003g0038 others(16): Show |
19 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+3419T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840741 | |||||||
chr5:60840786 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-86+3374G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840786 | |||||||
chr5:60840799 | G | A | 9 | a0001c0001t0007g0001 a0001c0001t0007g0029 a0001c0001t0007g0031 others(6): Show |
11 | HG00280.hp2 HG01192.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-86+3361C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60840799 | |||||||
chr5:60841006 | T | TA | 19 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0003g0038 others(16): Show |
19 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+3153dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841006 | |||||||
chr5:60841023 | C | CT | 5 | a0001c0001t0001g0045 a0001c0001t0001g0216 a0001c0001t0009g0243 others(2): Show |
5 | HG01981.hp1 HG02135.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+3136dupA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | |||||||
chr5:60841023 | CT | C | 94 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(91): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-86+3136delA | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | |||||||
chr5:60841023 | CTT | C | 7 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0028 others(4): Show |
7 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86+3135_-86+3136d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841023 | |||||||
chr5:60841075 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-86+3085C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841075 | |||||||
chr5:60841309 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0020g0128 |
3 | HG02572.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+2851T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841309 | |||||||
chr5:60841341 | A | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-86+2819T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841341 | |||||||
chr5:60841423 | A | G | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2737T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841423 | |||||||
chr5:60841426 | A | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2734T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841426 | |||||||
chr5:60841433 | T | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2727A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841433 | |||||||
chr5:60841435 | A | T | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2725T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841435 | |||||||
chr5:60841437 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2723A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841437 | |||||||
chr5:60841438 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2722C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841438 | |||||||
chr5:60841439 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2721C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841439 | |||||||
chr5:60841440 | G | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2720C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841440 | |||||||
chr5:60841441 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2719A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841441 | |||||||
chr5:60841443 | T | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(199): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-86+2717A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841443 | |||||||
chr5:60841448 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2712A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841448 | |||||||
chr5:60841450 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2710A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841450 | |||||||
chr5:60841467 | T | G | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2693A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841467 | |||||||
chr5:60841468 | CTTATCCT others(4): Show |
C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2681_-86+2691d others(13): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841468 | |||||||
chr5:60841480 | G | C | 1 | a0001c0001t0007g0036 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-86+2680C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841480 | |||||||
chr5:60841674 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-86+2486A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841674 | |||||||
chr5:60841778 | T | C | 3 | a0001c0001t0003g0199 a0001c0001t0011g0200 a0001c0001t0011g0201 |
3 | HG01109.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-86+2382A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60841778 | |||||||
chr5:60842003 | G | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-86+2157C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842003 | |||||||
chr5:60842032 | C | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-86+2128G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842032 | |||||||
chr5:60842132 | A | G | 38 | a0001c0001t0001g0171 a0001c0001t0001g0197 a0001c0001t0001g0198 others(35): Show |
39 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-86+2028T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842132 | |||||||
chr5:60842146 | A | C | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-86+2014T>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842146 | |||||||
chr5:60842233 | T | C | 1 | a0001c0001t0006g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-86+1927A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842233 | |||||||
chr5:60842460 | A | T | 7 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0008g0132 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+1700T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842460 | |||||||
chr5:60842496 | T | TA | 12 | a0001c0001t0001g0042 a0001c0001t0001g0122 a0001c0001t0001g0123 others(9): Show |
12 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+1663dupT | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842496 | |||||||
chr5:60842496 | T | TAA | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(88): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-86+1662_-86+1663d others(4): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842496 | |||||||
chr5:60842512 | G | T | 30 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(27): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+1648C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842512 | |||||||
chr5:60842516 | GCAGGGGG others(1): Show |
G | 10 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0207 others(7): Show |
10 | HG03490.hp2 HG03491.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.-86+1636_-86+1643d others(10): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842516 | |||||||
chr5:60842763 | C | T | 38 | a0001c0001t0001g0171 a0001c0001t0001g0197 a0001c0001t0001g0198 others(35): Show |
39 | HG00099.hp2 HG00673.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-86+1397G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842763 | |||||||
chr5:60842866 | T | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1294A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842866 | |||||||
chr5:60842869 | G | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1291C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842869 | |||||||
chr5:60842874 | T | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1286A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842874 | |||||||
chr5:60842875 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1285C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842875 | |||||||
chr5:60842880 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1280G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842880 | |||||||
chr5:60842881 | T | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1279A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842881 | |||||||
chr5:60842885 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1275G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842885 | |||||||
chr5:60842886 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1274T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842886 | |||||||
chr5:60842887 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0019g0041 |
2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-86+1273G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842887 | |||||||
chr5:60842891 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1269A>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842891 | |||||||
chr5:60842892 | A | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1268T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842892 | |||||||
chr5:60842895 | T | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1265A>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842895 | |||||||
chr5:60842897 | T | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1263A>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842897 | |||||||
chr5:60842900 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1260C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842900 | |||||||
chr5:60842901 | C | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1259G>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842901 | |||||||
chr5:60842902 | C | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1258G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842902 | |||||||
chr5:60842903 | A | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1257T>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842903 | |||||||
chr5:60842904 | C | CGTAGGGC others(1): Show |
90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(87): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+1255_-86+1256i others(10): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842904 | |||||||
chr5:60842905 | G | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-86+1255C>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60842905 | |||||||
chr5:60843022 | C | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86+1138G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843022 | |||||||
chr5:60843056 | C | G | 11 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86+1104G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843056 | |||||||
chr5:60843064 | G | A | 1 | a0001c0001t0025g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-86+1096C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843064 | |||||||
chr5:60843128 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-86+1032G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843128 | |||||||
chr5:60843211 | G | C | 2 | a0001c0001t0006g0163 a0001c0001t0023g0162 |
2 | HG01175.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-86+949C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843211 | |||||||
chr5:60843233 | G | A | 4 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0028 others(1): Show |
4 | HG01099.hp2 HG01168.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+927C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843233 | |||||||
chr5:60843259 | C | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0168 |
2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-86+901G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843259 | |||||||
chr5:60843336 | G | GGGGAAAG others(19): Show |
1 | a0001c0001t0018g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+798_-86+823dup others(26): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843336 | |||||||
chr5:60843336 | GGGGAAAG others(19): Show |
G | 30 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0011 others(27): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-86+798_-86+823del others(26): Show |
ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843336 | |||||||
chr5:60843337 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-86+823C>G | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843337 | |||||||
chr5:60843391 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-86+769C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843391 | |||||||
chr5:60843721 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(87): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-86+439G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843721 | |||||||
chr5:60843727 | C | G | 1 | a0001c0001t0003g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-86+433G>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843727 | |||||||
chr5:60843909 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+251C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843909 | |||||||
chr5:60843965 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-86+195C>T | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60843965 | |||||||
chr5:60844048 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-86+112G>A | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60844048 | |||||||
chr5:60844054 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(134): Show |
142 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86+106T>C | ELOVL7 | ENSG00000164181.14 | transcript | ENST00000508821.6 | protein_coding | 1/8 | chr5 | 60844054 |