Item | Value |
---|---|
geneid | 57486 |
ensemblid | ENSG00000123213.23 |
hgncid | 16058 |
symbol | NLN |
name | neurolysin |
refseq_nuc | NM_020726.5 |
refseq_prot | NP_065777.1 |
ensembl_nuc | ENST00000380985.10 |
ensembl_prot | ENSP00000370372.5 |
mane_status | MANE Select |
chr | chr5 |
start | 65722205 |
end | 65829283 |
strand | + |
ver | v1.2 |
region | chr5:65722205-65829283 |
region5000 | chr5:65717205-65834283 |
regionname0 | NLN_chr5_65722205_65829283 |
regionname5000 | NLN_chr5_65717205_65834283 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 704 | 292 | 56 | 63 | 126 | 14 | 31 | 106 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0002 | 0/0 | 704 | 25 | 21 | 3 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0003 | 0/0 | 704 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0004 | 0/0 | 704 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0005 | 0/0 | 704 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0006 | 0/0 | 704 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0007 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
a0008 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | MIARC others(699): Show |
chr5 | 65717205 | 65834283 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2112 | 204 | 52 | 42 | 74 | 10 | 25 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0002 | 1/0 | 2112 | 81 | 1 | 21 | 48 | 4 | 6 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0007 | 0/0 | 2112 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0011 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0013 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0014 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0001c0015 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0002c0003 | 0/0 | 2112 | 14 | 11 | 2 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0002c0004 | 0/0 | 2112 | 10 | 9 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0002c0016 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0003c0005 | 0/0 | 2112 | 7 | 6 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0004c0006 | 0/0 | 2112 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0005c0009 | 0/0 | 2112 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0006c0008 | 0/0 | 2112 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0007c0010 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 | ||
a0008c0012 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | ATGAT others(2107): Show |
chr5 | 65717205 | 65834283 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8652 | 33 | 4 | 10 | 5 | 4 | 10 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0002 | 0/0 | 8652 | 45 | 4 | 10 | 26 | 1 | 4 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0003 | 0/0 | 8652 | 22 | 0 | 5 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0004 | 0/0 | 8652 | 20 | 5 | 6 | 6 | 3 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0005 | 0/0 | 8652 | 18 | 1 | 0 | 15 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0006 | 0/0 | 8652 | 9 | 8 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0007 | 0/0 | 8651 | 2 | 0 | 1 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0008 | 0/0 | 8652 | 7 | 7 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0009 | 0/0 | 8652 | 8 | 0 | 6 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0011 | 0/0 | 8652 | 4 | 1 | 0 | 0 | 2 | 1 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0014 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0015 | 0/0 | 8652 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0019 | 0/0 | 8652 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0021 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8643): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0024 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0025 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0026 | 0/0 | 8652 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0027 | 0/0 | 8652 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0028 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0030 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8643): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0031 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0032 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0033 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0036 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0037 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0039 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0042 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0046 | 0/1 | 8649 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8644): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0047 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0048 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0050 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0051 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0052 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0053 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0055 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8657): Show |
chr5 | 65717205 | 65834283 |
a0001c0001t0056 | 0/0 | 8652 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0001 | 1/0 | 8652 | 70 | 1 | 19 | 39 | 4 | 6 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0004 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0012 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0013 | 0/0 | 8652 | 4 | 0 | 0 | 4 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0045 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0002t0054 | 0/0 | 8652 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0007t0018 | 0/0 | 8652 | 3 | 0 | 0 | 3 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0011t0005 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0013t0038 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0014t0057 | 0/0 | 8652 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0001c0015t0004 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0007 | 0/0 | 8651 | 4 | 1 | 2 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0010 | 0/0 | 8651 | 6 | 6 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0017 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0041 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0049 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0003t0058 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0004t0007 | 0/0 | 8651 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0004t0016 | 0/0 | 8651 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0004t0017 | 0/0 | 8651 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0004t0040 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0004t0043 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0002c0016t0034 | 0/0 | 8651 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0003c0005t0020 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0003c0005t0021 | 0/0 | 8648 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8643): Show |
chr5 | 65717205 | 65834283 |
a0003c0005t0022 | 0/0 | 8652 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0003c0005t0023 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0004c0006t0001 | 0/0 | 8652 | 4 | 4 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0004c0006t0008 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0004c0006t0029 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0005c0009t0035 | 0/0 | 8651 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8646): Show |
chr5 | 65717205 | 65834283 |
a0005c0009t0044 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0006c0008t0006 | 0/0 | 8652 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0007c0010t0001 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
a0008c0012t0001 | 0/0 | 8652 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | AGGCG others(8647): Show |
chr5 | 65717205 | 65834283 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0008g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0015g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0019g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0021g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0024g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0024g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0025g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0026g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0026g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0027g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0027g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0028g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0030g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0032g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0033g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0036g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0037g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0039g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0042g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0046g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0047g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0048g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0050g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0051g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0052g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0053g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0055g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0001t0056g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0012g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0013g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0013g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0013g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0045g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0002t0054g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0007t0018g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0007t0018g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0007t0018g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0011t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0013t0038g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0014t0057g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0001c0015t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0041g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0049g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0003t0058g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0016g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0016g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0017g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0017g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0040g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0004t0043g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0002c0016t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0020g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0022g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0023g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0003c0005t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0004c0006t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0004c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0004c0006t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0004c0006t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0004c0006t0029g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0005c0009t0035g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0005c0009t0044g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0006c0008t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0006c0008t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0007c0010t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
a0008c0012t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0039 | EUR | GBR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | FIN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00438 | hp1 | a0001 | c0007 | t0018 | g0291 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00609 | hp2 | a0001 | c0002 | t0013 | g0162 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0300 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00738 | hp1 | a0002 | c0003 | t0007 | g0137 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0242 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01071 | hp2 | a0001 | c0001 | t0055 | g0304 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0132 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0287 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01109 | hp1 | a0001 | c0001 | t0019 | g0019 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01167 | hp2 | a0002 | c0004 | t0017 | g0292 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0069 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01243 | hp1 | a0005 | c0009 | t0035 | g0255 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01243 | hp2 | a0003 | c0005 | t0022 | g0083 | AMR | PUR | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01256 | hp1 | a0002 | c0003 | t0007 | g0228 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0214 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0270 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0227 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0235 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0290 | EUR | IBS | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01884 | hp1 | a0001 | c0001 | t0031 | g0254 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01884 | hp2 | a0002 | c0003 | t0041 | g0089 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01891 | hp1 | a0001 | c0001 | t0030 | g0059 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01891 | hp2 | a0001 | c0001 | t0025 | g0020 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01934 | hp1 | a0001 | c0001 | t0009 | g0027 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0058 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01975 | hp1 | a0001 | c0001 | t0009 | g0116 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01981 | hp1 | a0001 | c0002 | t0054 | g0272 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02004 | hp2 | a0001 | c0001 | t0037 | g0007 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02027 | hp2 | a0001 | c0002 | t0013 | g0128 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02040 | hp2 | a0001 | c0002 | t0013 | g0012 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02055 | hp1 | a0005 | c0009 | t0044 | g0042 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02055 | hp2 | a0002 | c0003 | t0010 | g0267 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02056 | hp1 | a0001 | c0001 | t0014 | g0131 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02129 | hp2 | a0001 | c0002 | t0013 | g0012 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02132 | hp1 | a0001 | c0014 | t0057 | g0306 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | KHV | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02145 | hp2 | a0002 | c0003 | t0007 | g0085 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02257 | hp1 | a0002 | c0016 | t0034 | g0256 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02258 | hp2 | a0002 | c0004 | t0043 | g0258 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02280 | hp1 | a0002 | c0003 | t0010 | g0286 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0250 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02451 | hp1 | a0004 | c0006 | t0001 | g0101 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02451 | hp2 | a0001 | c0001 | t0051 | g0298 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02572 | hp2 | a0001 | c0001 | t0021 | g0097 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02622 | hp1 | a0003 | c0005 | t0023 | g0087 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02630 | hp1 | a0001 | c0001 | t0024 | g0045 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02647 | hp1 | a0002 | c0004 | t0016 | g0088 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02647 | hp2 | a0003 | c0005 | t0023 | g0060 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02717 | hp1 | a0001 | c0015 | t0004 | g0263 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02717 | hp2 | a0001 | c0001 | t0048 | g0264 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02723 | hp1 | a0002 | c0003 | t0010 | g0260 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02723 | hp2 | a0001 | c0001 | t0033 | g0218 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02809 | hp1 | a0001 | c0001 | t0028 | g0179 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02809 | hp2 | a0001 | c0001 | t0042 | g0109 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0043 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02818 | hp2 | a0001 | c0001 | t0039 | g0151 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02886 | hp1 | a0002 | c0003 | t0049 | g0268 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02895 | hp2 | a0002 | c0003 | t0058 | g0284 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02896 | hp1 | a0002 | c0004 | t0040 | g0310 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02896 | hp2 | a0003 | c0005 | t0020 | g0018 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0243 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02897 | hp2 | a0003 | c0005 | t0020 | g0018 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02965 | hp1 | a0002 | c0004 | t0016 | g0061 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02965 | hp2 | a0002 | c0004 | t0007 | g0248 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02970 | hp1 | a0001 | c0001 | t0047 | g0247 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02970 | hp2 | a0001 | c0001 | t0025 | g0020 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02976 | hp2 | a0006 | c0008 | t0006 | g0103 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03041 | hp2 | a0001 | c0011 | t0005 | g0021 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03098 | hp1 | a0002 | c0004 | t0016 | g0063 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03130 | hp2 | a0002 | c0004 | t0007 | g0244 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03139 | hp2 | a0002 | c0004 | t0007 | g0245 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03195 | hp2 | a0002 | c0003 | t0010 | g0282 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03209 | hp2 | a0001 | c0001 | t0050 | g0309 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03225 | hp1 | a0004 | c0006 | t0008 | g0221 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03225 | hp2 | a0003 | c0005 | t0022 | g0084 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03486 | hp1 | a0004 | c0006 | t0029 | g0108 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03490 | hp2 | a0001 | c0001 | t0026 | g0278 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03492 | hp1 | a0001 | c0001 | t0026 | g0294 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03516 | hp1 | a0002 | c0003 | t0010 | g0269 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | ESN | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03540 | hp2 | a0008 | c0012 | t0001 | g0106 | AFR | GWD | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03579 | hp1 | a0006 | c0008 | t0006 | g0177 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03579 | hp2 | a0002 | c0004 | t0017 | g0277 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03669 | hp2 | a0001 | c0001 | t0009 | g0024 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03688 | hp1 | a0001 | c0001 | t0056 | g0259 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0068 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04115 | hp1 | a0002 | c0003 | t0007 | g0229 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0062 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | STU | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | CHB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18941 | hp1 | a0001 | c0002 | t0012 | g0176 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18957 | hp2 | a0001 | c0002 | t0012 | g0174 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18962 | hp1 | a0001 | c0007 | t0018 | g0289 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18968 | hp2 | a0001 | c0002 | t0012 | g0003 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18983 | hp1 | a0001 | c0001 | t0014 | g0150 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18991 | hp2 | a0001 | c0001 | t0027 | g0307 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18993 | hp1 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19000 | hp2 | a0001 | c0001 | t0036 | g0026 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19006 | hp2 | a0001 | c0007 | t0018 | g0303 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19009 | hp1 | a0001 | c0002 | t0045 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19012 | hp2 | a0001 | c0001 | t0027 | g0308 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19030 | hp1 | a0004 | c0006 | t0001 | g0107 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19030 | hp2 | a0002 | c0003 | t0017 | g0266 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19043 | hp1 | a0002 | c0003 | t0010 | g0285 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19043 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19054 | hp1 | a0001 | c0001 | t0014 | g0130 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19083 | hp1 | a0001 | c0002 | t0012 | g0175 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19089 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | YRI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20129 | hp1 | a0001 | c0001 | t0024 | g0048 | AFR | ASW | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0276 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0111 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20905 | hp1 | a0001 | c0001 | t0011 | g0236 | SAS | GIH | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02109 | hp1 | a0001 | c0001 | t0052 | g0283 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0249 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02559 | hp1 | a0001 | c0001 | t0032 | g0220 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | ACB | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03471 | hp1 | a0007 | c0010 | t0001 | g0105 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG03471 | hp2 | a0003 | c0005 | t0021 | g0086 | AFR | MSL | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG06807 | hp1 | a0001 | c0001 | t0019 | g0019 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0222 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0219 | AFR | USA | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA21309 | hp1 | a0001 | c0013 | t0038 | g0022 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
NA21309 | hp2 | a0001 | c0001 | t0053 | g0299 | AFR | LWK | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
homoSapiens | chm13v2 | a0001 | c0001 | t0046 | g0241 | REF | REF | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0075 | REF | REF | NLN_chr5_65717205_65834283 | NLN | chr5 | 65717205 | 65834283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65758760 | G | A | 3 | a0004 a0006 a0007 |
9 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(6): Show |
missense_variant | MODERATE | c.235G>A | p.Gly79Ser | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 404/8652 | 235/2115 | 79/704 | chr5 | 65758760 | |||
chr5:65785895 | G | A | 2 | a0007 a0008 |
2 | HG03471.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.943G>A | p.Val315Ile | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/13 | 1112/8652 | 943/2115 | 315/704 | chr5 | 65785895 | |||
chr5:65788274 | A | G | 3 | a0003 a0005 a0006 |
11 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(8): Show |
missense_variant | MODERATE | c.1115A>G | p.Lys372Arg | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/13 | 1284/8652 | 1115/2115 | 372/704 | chr5 | 65788274 | |||
chr5:65822910 | C | T | 2 | a0002 a0005 |
27 | HG00738.hp1 HG01167.hp2 HG01243.hp1 others(24): Show |
missense_variant | MODERATE | c.2110C>T | p.Pro704Ser | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2279/8652 | 2110/2115 | 704/704 | chr5 | 65822910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65758741 | C | T | 1 | a0002c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.216C>T | p.Tyr72Tyr | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 385/8652 | 216/2115 | 72/704 | chr5 | 65758741 | |||
chr5:65758795 | G | A | 1 | a0001c0011 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.270G>A | p.Gln90Gln | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/13 | 439/8652 | 270/2115 | 90/704 | chr5 | 65758795 | |||
chr5:65785858 | C | T | 1 | a0001c0007 | 3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
synonymous_variant | LOW | c.906C>T | p.Phe302Phe | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/13 | 1075/8652 | 906/2115 | 302/704 | chr5 | 65785858 | |||
chr5:65788143 | C | T | 1 | a0001c0015 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.984C>T | p.Pro328Pro | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/13 | 1153/8652 | 984/2115 | 328/704 | chr5 | 65788143 | |||
chr5:65792595 | C | T | 1 | a0001c0014 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.1467C>T | p.His489His | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/13 | 1636/8652 | 1467/2115 | 489/704 | chr5 | 65792595 | |||
chr5:65812292 | G | A | 1 | a0001c0013 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1881G>A | p.Gly627Gly | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/13 | 2050/8652 | 1881/2115 | 627/704 | chr5 | 65812292 | |||
chr5:65812388 | A | G | 14 | a0001c0001 a0001c0007 a0001c0011 others(11): Show |
240 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(237): Show |
synonymous_variant | LOW | c.1977A>G | p.Pro659Pro | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/13 | 2146/8652 | 1977/2115 | 659/704 | chr5 | 65812388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65722299 | C | G | 21 | a0001c0001t0004 a0001c0001t0025 a0001c0001t0026 others(18): Show |
51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 75 | chr5 | 65722299 | ||||||
chr5:65722315 | C | T | 1 | a0001c0001t0014 | 4 | HG02056.hp1 NA18983.hp1 NA18993.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 59 | chr5 | 65722315 | ||||||
chr5:65722351 | G | T | 1 | a0002c0003t0058 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/13 | 23 | chr5 | 65722351 | ||||||
chr5:65823063 | A | C | 1 | a0001c0001t0024 | 2 | HG02630.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 148 | chr5 | 65823063 | ||||||
chr5:65823292 | G | A | 1 | a0001c0001t0019 | 2 | HG01109.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 377 | chr5 | 65823292 | ||||||
chr5:65823352 | G | A | 7 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0019 others(4): Show |
28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 437 | chr5 | 65823352 | ||||||
chr5:65823368 | T | C | 1 | a0002c0003t0049 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 453 | chr5 | 65823368 | ||||||
chr5:65823788 | A | G | 1 | a0001c0001t0047 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 873 | chr5 | 65823788 | ||||||
chr5:65824054 | A | G | 1 | a0003c0005t0023 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1139 | chr5 | 65824054 | ||||||
chr5:65824144 | T | A | 2 | a0001c0001t0015 a0001c0001t0050 |
4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1229 | chr5 | 65824144 | ||||||
chr5:65824199 | G | A | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(20): Show |
97 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1284G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1284 | chr5 | 65824199 | ||||||
chr5:65824226 | C | T | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(14): Show |
93 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1311C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1311 | chr5 | 65824226 | ||||||
chr5:65824316 | T | C | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
171 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1401T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1401 | chr5 | 65824316 | ||||||
chr5:65824437 | CA | C | 16 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(13): Show |
31 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1523delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1523 | chr5 | 65824437 | ||||||
chr5:65824544 | T | C | 16 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(13): Show |
31 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1629T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1629 | chr5 | 65824544 | ||||||
chr5:65824582 | G | T | 1 | a0003c0005t0022 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1667 | chr5 | 65824582 | ||||||
chr5:65824693 | T | C | 1 | a0001c0001t0025 | 2 | HG01891.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1778T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1778 | chr5 | 65824693 | ||||||
chr5:65824770 | G | A | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0036 others(2): Show |
35 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1855G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1855 | chr5 | 65824770 | ||||||
chr5:65824828 | G | A | 1 | a0005c0009t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1913G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1913 | chr5 | 65824828 | ||||||
chr5:65824875 | G | C | 15 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(12): Show |
30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1960G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1960 | chr5 | 65824875 | ||||||
chr5:65824910 | G | A | 15 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(12): Show |
30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1995G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 1995 | chr5 | 65824910 | ||||||
chr5:65825025 | C | T | 1 | a0001c0001t0042 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2110 | chr5 | 65825025 | ||||||
chr5:65825162 | TTCTC | T | 3 | a0001c0001t0021 a0001c0001t0030 a0003c0005t0021 |
3 | HG01891.hp1 HG02572.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2249_*2252delCTCT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2249 | INFO_REALIGN_3_PRIME | chr5 | 65825162 | |||||
chr5:65825365 | T | C | 15 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(12): Show |
30 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2450T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2450 | chr5 | 65825365 | ||||||
chr5:65825480 | A | G | 1 | a0001c0001t0027 | 2 | NA18991.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2565A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2565 | chr5 | 65825480 | ||||||
chr5:65825499 | G | C | 1 | a0001c0001t0052 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2584G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2584 | chr5 | 65825499 | ||||||
chr5:65825540 | G | A | 32 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(29): Show |
105 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2625G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2625 | chr5 | 65825540 | ||||||
chr5:65825687 | G | A | 2 | a0001c0001t0039 a0001c0002t0054 |
2 | HG01981.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2772G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2772 | chr5 | 65825687 | ||||||
chr5:65825835 | T | C | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0036 others(3): Show |
36 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2920T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 2920 | chr5 | 65825835 | ||||||
chr5:65826006 | A | G | 9 | a0001c0001t0007 a0002c0003t0007 a0002c0003t0010 others(6): Show |
21 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3091A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3091 | chr5 | 65826006 | ||||||
chr5:65826138 | C | A | 1 | a0002c0003t0041 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3223C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3223 | chr5 | 65826138 | ||||||
chr5:65826199 | T | C | 13 | a0001c0001t0007 a0001c0001t0042 a0002c0003t0007 others(10): Show |
28 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3284T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3284 | chr5 | 65826199 | ||||||
chr5:65826219 | A | G | 3 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0051 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3304A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3304 | chr5 | 65826219 | ||||||
chr5:65826255 | C | T | 1 | a0001c0001t0037 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3340C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3340 | chr5 | 65826255 | ||||||
chr5:65826256 | G | C | 1 | a0005c0009t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3341G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3341 | chr5 | 65826256 | ||||||
chr5:65826262 | A | T | 1 | a0001c0001t0042 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3347A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3347 | chr5 | 65826262 | ||||||
chr5:65826300 | T | C | 1 | a0002c0004t0040 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3385T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3385 | chr5 | 65826300 | ||||||
chr5:65826380 | G | C | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0036 others(2): Show |
35 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3465G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3465 | chr5 | 65826380 | ||||||
chr5:65826474 | C | T | 1 | a0001c0001t0056 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3559C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 3559 | chr5 | 65826474 | ||||||
chr5:65826996 | C | A | 1 | a0003c0005t0023 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4081C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4081 | chr5 | 65826996 | ||||||
chr5:65827005 | G | C | 13 | a0001c0001t0007 a0001c0001t0028 a0001c0001t0042 others(10): Show |
27 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4090G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4090 | chr5 | 65827005 | ||||||
chr5:65827007 | G | C | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4092G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4092 | chr5 | 65827007 | ||||||
chr5:65827009 | A | T | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4094A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4094 | chr5 | 65827009 | ||||||
chr5:65827010 | A | C | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4095A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4095 | chr5 | 65827010 | ||||||
chr5:65827012 | T | A | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4097T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4097 | chr5 | 65827012 | ||||||
chr5:65827015 | C | A | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4100C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4100 | chr5 | 65827015 | ||||||
chr5:65827016 | C | G | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4101C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4101 | chr5 | 65827016 | ||||||
chr5:65827017 | A | G | 2 | a0002c0004t0040 a0005c0009t0035 |
2 | HG01243.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4102A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4102 | chr5 | 65827017 | ||||||
chr5:65827018 | C | T | 1 | a0001c0001t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4103C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4103 | chr5 | 65827018 | ||||||
chr5:65827139 | C | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(37): Show |
158 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*4224C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4224 | chr5 | 65827139 | ||||||
chr5:65827274 | G | A | 7 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0019 others(4): Show |
28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4359G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4359 | chr5 | 65827274 | ||||||
chr5:65827598 | T | A | 3 | a0002c0003t0010 a0002c0003t0049 a0002c0003t0058 |
8 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4683T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4683 | chr5 | 65827598 | ||||||
chr5:65827740 | G | A | 1 | a0004c0006t0029 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4825G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4825 | chr5 | 65827740 | ||||||
chr5:65827758 | T | C | 1 | a0002c0004t0040 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4843 | chr5 | 65827758 | ||||||
chr5:65827761 | A | C | 1 | a0001c0001t0026 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4846A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 4846 | chr5 | 65827761 | ||||||
chr5:65827977 | G | A | 1 | a0001c0001t0009 | 8 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5062G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5062 | chr5 | 65827977 | ||||||
chr5:65828002 | G | A | 1 | a0001c0001t0036 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5087G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5087 | chr5 | 65828002 | ||||||
chr5:65828214 | C | T | 1 | a0001c0002t0045 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5299C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5299 | chr5 | 65828214 | ||||||
chr5:65828229 | A | C | 4 | a0001c0001t0024 a0002c0004t0016 a0002c0016t0034 others(1): Show |
7 | HG02055.hp1 HG02257.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5314A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5314 | chr5 | 65828229 | ||||||
chr5:65828254 | G | GAAAATAA others(3): Show |
1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5341_*5342insAATA others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5342 | INFO_REALIGN_3_PRIME | chr5 | 65828254 | |||||
chr5:65828257 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5342G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5342 | chr5 | 65828257 | ||||||
chr5:65828258 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5343T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5343 | chr5 | 65828258 | ||||||
chr5:65828260 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5345T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5345 | chr5 | 65828260 | ||||||
chr5:65828261 | G | T | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5346G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5346 | chr5 | 65828261 | ||||||
chr5:65828262 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5347T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5347 | chr5 | 65828262 | ||||||
chr5:65828263 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5348G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5348 | chr5 | 65828263 | ||||||
chr5:65828264 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5349 | chr5 | 65828264 | ||||||
chr5:65828265 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5350C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5350 | chr5 | 65828265 | ||||||
chr5:65828268 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5353G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5353 | chr5 | 65828268 | ||||||
chr5:65828271 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5356C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5356 | chr5 | 65828271 | ||||||
chr5:65828276 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5361G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5361 | chr5 | 65828276 | ||||||
chr5:65828279 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5364 | chr5 | 65828279 | ||||||
chr5:65828292 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5377C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5377 | chr5 | 65828292 | ||||||
chr5:65828293 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5378T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5378 | chr5 | 65828293 | ||||||
chr5:65828294 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5379C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5379 | chr5 | 65828294 | ||||||
chr5:65828295 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5380C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5380 | chr5 | 65828295 | ||||||
chr5:65828297 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5382G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5382 | chr5 | 65828297 | ||||||
chr5:65828298 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5383T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5383 | chr5 | 65828298 | ||||||
chr5:65828299 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5384G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5384 | chr5 | 65828299 | ||||||
chr5:65828303 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5388G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5388 | chr5 | 65828303 | ||||||
chr5:65828305 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5390T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5390 | chr5 | 65828305 | ||||||
chr5:65828306 | C | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5391C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5391 | chr5 | 65828306 | ||||||
chr5:65828310 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5395T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5395 | chr5 | 65828310 | ||||||
chr5:65828314 | G | T | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5399 | chr5 | 65828314 | ||||||
chr5:65828315 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5400T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5400 | chr5 | 65828315 | ||||||
chr5:65828316 | T | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5401T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5401 | chr5 | 65828316 | ||||||
chr5:65828317 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5402G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5402 | chr5 | 65828317 | ||||||
chr5:65828318 | G | A | 1 | a0001c0001t0055 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5403G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5403 | chr5 | 65828318 | ||||||
chr5:65828429 | A | C | 1 | a0001c0001t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5514A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5514 | chr5 | 65828429 | ||||||
chr5:65828587 | C | T | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(32): Show |
123 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*5672C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5672 | chr5 | 65828587 | ||||||
chr5:65828715 | C | T | 1 | a0003c0005t0023 | 2 | HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5800C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5800 | chr5 | 65828715 | ||||||
chr5:65828750 | T | G | 20 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(17): Show |
65 | HG00438.hp1 HG00609.hp1 HG00738.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*5835T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5835 | chr5 | 65828750 | ||||||
chr5:65828775 | C | T | 1 | a0001c0002t0012 | 4 | NA18941.hp1 NA18957.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5860C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 5860 | chr5 | 65828775 | ||||||
chr5:65828952 | A | AC | 2 | a0001c0001t0042 a0003c0005t0023 |
3 | HG02622.hp1 HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6039dupC | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6040 | INFO_REALIGN_3_PRIME | chr5 | 65828952 | |||||
chr5:65829162 | A | G | 1 | a0001c0001t0011 | 4 | HG01516.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6247A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6247 | chr5 | 65829162 | ||||||
chr5:65829238 | A | G | 1 | a0003c0005t0022 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6323A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 13/13 | 6323 | chr5 | 65829238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65722494 | C | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+80C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722494 | |||||||
chr5:65722723 | A | G | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+309A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722723 | |||||||
chr5:65722959 | T | C | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+545T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65722959 | |||||||
chr5:65723104 | C | A | 2 | a0001c0011t0005g0021 a0001c0013t0038g0022 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.41+690C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723104 | |||||||
chr5:65723315 | T | C | 1 | a0001c0001t0056g0259 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.41+901T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723315 | |||||||
chr5:65723552 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+1138T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723552 | |||||||
chr5:65723577 | G | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+1163G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723577 | |||||||
chr5:65723629 | A | G | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+1215A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723629 | |||||||
chr5:65723659 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.41+1245C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723659 | |||||||
chr5:65723696 | T | C | 1 | a0002c0003t0010g0260 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41+1282T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723696 | |||||||
chr5:65723699 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.41+1285C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723699 | |||||||
chr5:65723739 | C | T | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+1325C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723739 | |||||||
chr5:65723763 | C | G | 51 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(48): Show |
52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+1349C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65723763 | |||||||
chr5:65723814 | C | CA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(17): Show |
21 | HG00099.hp1 HG01123.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+1422dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(2): Show |
8 | a0001c0001t0004g0301 a0001c0001t0004g0302 a0001c0001t0004g0305 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+1414_41+1422dup others(9): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0004g0288 a0001c0001t0004g0290 a0001c0001t0004g0293 others(17): Show |
20 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.41+1413_41+1422dup others(10): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(4): Show |
17 | a0001c0001t0004g0270 a0001c0001t0004g0271 a0001c0001t0004g0273 others(14): Show |
18 | HG01106.hp1 HG01261.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.41+1412_41+1422dup others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(5): Show |
1 | a0002c0003t0017g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+1411_41+1422dup others(12): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0004g0265 a0002c0004t0040g0310 |
2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41+1410_41+1422dup others(13): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0048g0264 a0001c0015t0004g0263 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.41+1409_41+1422dup others(14): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+1407_41+1422dup others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(10): Show |
1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+1406_41+1422dup others(17): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | C | CAAAAAAA others(11): Show |
1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+1405_41+1422dup others(18): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | CA | C | 35 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0001g0239 others(32): Show |
35 | HG01070.hp2 HG01256.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.41+1422delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65723814 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+1410_41+1422del others(13): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65723814 | ||||||
chr5:65724018 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+1604G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724018 | |||||||
chr5:65724112 | T | A | 1 | a0001c0001t0002g0041 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.41+1698T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724112 | |||||||
chr5:65724249 | TAACTGCC others(10): Show |
T | 1 | a0001c0002t0001g0215 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.41+1836_41+1852del others(17): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724249 | |||||||
chr5:65724261 | A | G | 92 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(89): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.41+1847A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724261 | |||||||
chr5:65724348 | T | C | 3 | a0001c0001t0052g0283 a0002c0003t0010g0267 a0002c0003t0010g0282 |
3 | HG02055.hp2 HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.41+1934T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724348 | |||||||
chr5:65724427 | T | C | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+2013T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724427 | |||||||
chr5:65724543 | T | C | 1 | a0001c0001t0015g0043 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41+2129T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724543 | |||||||
chr5:65724557 | A | G | 1 | a0001c0001t0009g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.41+2143A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724557 | |||||||
chr5:65724701 | T | C | 9 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+2287T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724701 | |||||||
chr5:65724789 | GTTTCTTT others(4): Show |
G | 1 | a0001c0013t0038g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+2390_41+2400del others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65724789 | ||||||
chr5:65724804 | C | T | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2390C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724804 | |||||||
chr5:65724804 | CT | C | 50 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(47): Show |
51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.41+2405delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65724804 | ||||||
chr5:65724805 | T | C | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2391T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724805 | |||||||
chr5:65724871 | G | T | 9 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+2457G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724871 | |||||||
chr5:65724978 | T | A | 34 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(31): Show |
34 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.41+2564T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724978 | |||||||
chr5:65724996 | G | A | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+2582G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65724996 | |||||||
chr5:65725027 | G | T | 1 | a0001c0002t0001g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.41+2613G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725027 | |||||||
chr5:65725085 | G | A | 1 | a0001c0001t0005g0052 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.41+2671G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725085 | |||||||
chr5:65725289 | A | G | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+2875A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725289 | |||||||
chr5:65725339 | T | C | 6 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0003g0055 others(3): Show |
6 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+2925T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725339 | |||||||
chr5:65725510 | A | G | 1 | a0001c0002t0001g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.41+3096A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725510 | |||||||
chr5:65725842 | G | A | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+3428G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725842 | |||||||
chr5:65725895 | G | A | 34 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(31): Show |
34 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.41+3481G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725895 | |||||||
chr5:65725897 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(153): Show |
165 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.41+3483A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725897 | |||||||
chr5:65725929 | G | A | 1 | a0001c0002t0004g0287 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.41+3515G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725929 | |||||||
chr5:65725969 | G | A | 5 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0002t0012g0174 others(2): Show |
5 | HG02040.hp1 NA18941.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+3555G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725969 | |||||||
chr5:65725972 | C | T | 1 | a0001c0002t0001g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.41+3558C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65725972 | |||||||
chr5:65726010 | G | A | 1 | a0001c0001t0030g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.41+3596G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726010 | |||||||
chr5:65726106 | C | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(48): Show |
57 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.41+3692C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726106 | |||||||
chr5:65726111 | C | CA | 21 | a0001c0001t0001g0037 a0001c0001t0001g0216 a0001c0001t0002g0223 others(18): Show |
21 | HG00741.hp2 HG02559.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+3716dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | ||||||
chr5:65726111 | CA | C | 103 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(100): Show |
113 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.41+3716delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | ||||||
chr5:65726111 | CAA | C | 11 | a0001c0001t0002g0257 a0001c0001t0004g0301 a0001c0001t0005g0261 others(8): Show |
13 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+3715_41+3716del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | ||||||
chr5:65726111 | CAAA | C | 49 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.41+3714_41+3716del others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65726111 | ||||||
chr5:65726114 | A | C | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+3700A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726114 | |||||||
chr5:65726131 | T | A | 1 | a0003c0005t0023g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+3717T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726131 | |||||||
chr5:65726280 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+3866A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726280 | |||||||
chr5:65726386 | G | A | 55 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(52): Show |
58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+3972G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726386 | |||||||
chr5:65726587 | G | A | 1 | a0001c0001t0021g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41+4173G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726587 | |||||||
chr5:65726684 | T | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4270T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726684 | |||||||
chr5:65726700 | A | G | 2 | a0001c0001t0006g0047 a0001c0001t0024g0048 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.41+4286A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726700 | |||||||
chr5:65726719 | A | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4305A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726719 | |||||||
chr5:65726734 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+4320G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726734 | |||||||
chr5:65726740 | C | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+4326C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726740 | |||||||
chr5:65726965 | T | G | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.41+4551T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65726965 | |||||||
chr5:65727014 | T | TG | 58 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(55): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+4600_41+4601ins others(1): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727014 | |||||||
chr5:65727015 | C | A | 58 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(55): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+4601C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727015 | |||||||
chr5:65727261 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.41+4847G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727261 | |||||||
chr5:65727295 | G | A | 51 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(48): Show |
52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+4881G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727295 | |||||||
chr5:65727370 | A | G | 55 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(52): Show |
58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+4956A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727370 | |||||||
chr5:65727541 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(52): Show |
61 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.41+5127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727541 | |||||||
chr5:65727559 | T | C | 1 | a0002c0004t0016g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41+5145T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727559 | |||||||
chr5:65727575 | G | A | 4 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(1): Show |
4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+5161G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727575 | |||||||
chr5:65727821 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0028g0179 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+5407C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727821 | |||||||
chr5:65727912 | C | G | 280 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(277): Show |
301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.41+5498C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727912 | |||||||
chr5:65727923 | C | T | 1 | a0001c0011t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.41+5509C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65727923 | |||||||
chr5:65728100 | A | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+5686A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728100 | |||||||
chr5:65728138 | A | G | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0169 others(2): Show |
5 | NA18949.hp1 NA18992.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+5724A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728138 | |||||||
chr5:65728188 | A | G | 2 | a0001c0002t0001g0167 a0001c0002t0001g0215 |
2 | NA18988.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.41+5774A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728188 | |||||||
chr5:65728454 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.41+6040T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728454 | |||||||
chr5:65728520 | C | A | 1 | a0002c0003t0058g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.41+6106C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728520 | |||||||
chr5:65728859 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0028g0179 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+6445T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728859 | |||||||
chr5:65728936 | C | T | 2 | a0002c0004t0016g0061 a0002c0004t0016g0063 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.41+6522C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728936 | |||||||
chr5:65728947 | G | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0005g0261 others(5): Show |
10 | HG01109.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+6533G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728947 | |||||||
chr5:65728969 | G | A | 19 | a0001c0001t0004g0270 a0001c0001t0004g0271 a0001c0001t0004g0273 others(16): Show |
19 | HG00438.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.41+6555G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65728969 | |||||||
chr5:65729272 | A | C | 93 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(90): Show |
101 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.41+6858A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729272 | |||||||
chr5:65729318 | G | GTATCAAT others(16): Show |
7 | a0001c0001t0002g0246 a0001c0001t0015g0249 a0001c0001t0015g0250 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6904_41+6905ins others(23): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729318 | |||||||
chr5:65729321 | T | A | 7 | a0001c0001t0002g0246 a0001c0001t0015g0249 a0001c0001t0015g0250 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6907T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729321 | |||||||
chr5:65729322 | G | T | 7 | a0001c0001t0002g0246 a0001c0001t0015g0249 a0001c0001t0015g0250 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6908G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729322 | |||||||
chr5:65729323 | A | C | 7 | a0001c0001t0002g0246 a0001c0001t0015g0249 a0001c0001t0015g0250 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6909A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729323 | |||||||
chr5:65729324 | C | A | 7 | a0001c0001t0002g0246 a0001c0001t0015g0249 a0001c0001t0015g0250 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+6910C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729324 | |||||||
chr5:65729369 | C | CT | 9 | a0001c0001t0001g0163 a0001c0001t0002g0080 a0001c0001t0002g0081 others(6): Show |
9 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+6978dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | ||||||
chr5:65729369 | CT | C | 88 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(85): Show |
95 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.41+6978delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | ||||||
chr5:65729369 | CTT | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0178 others(58): Show |
66 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.41+6977_41+6978del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | ||||||
chr5:65729369 | CTTT | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0180 a0001c0001t0002g0013 others(2): Show |
6 | HG00323.hp2 HG03017.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+6976_41+6978del others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65729369 | ||||||
chr5:65729394 | G | A | 187 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(184): Show |
200 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.41+6980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729394 | |||||||
chr5:65729422 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7008T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729422 | |||||||
chr5:65729462 | C | T | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.41+7048C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729462 | |||||||
chr5:65729621 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7207G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729621 | |||||||
chr5:65729654 | G | A | 3 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 |
3 | NA18948.hp2 NA18954.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.41+7240G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729654 | |||||||
chr5:65729658 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7244A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729658 | |||||||
chr5:65729666 | G | A | 55 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(52): Show |
58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+7252G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729666 | |||||||
chr5:65729789 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.41+7375A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729789 | |||||||
chr5:65729822 | A | G | 12 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(9): Show |
13 | NA18942.hp1 NA18962.hp2 NA18964.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+7408A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729822 | |||||||
chr5:65729883 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+7469G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65729883 | |||||||
chr5:65730004 | C | T | 1 | a0002c0003t0041g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41+7590C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730004 | |||||||
chr5:65730237 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.41+7823G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730237 | |||||||
chr5:65730352 | A | G | 1 | a0001c0013t0038g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+7938A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730352 | |||||||
chr5:65730392 | G | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(153): Show |
167 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.41+7978G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730392 | |||||||
chr5:65730393 | G | C | 1 | a0001c0001t0008g0002 | 3 | HG02258.hp1 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.41+7979G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730393 | |||||||
chr5:65730543 | CT | C | 7 | a0001c0001t0001g0038 a0001c0001t0002g0225 a0001c0001t0003g0067 others(4): Show |
8 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+8142delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65730543 | ||||||
chr5:65730562 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+8148A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730562 | |||||||
chr5:65730613 | A | G | 1 | a0006c0008t0006g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.41+8199A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730613 | |||||||
chr5:65730684 | G | A | 2 | a0001c0001t0021g0097 a0001c0001t0030g0059 |
2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.41+8270G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730684 | |||||||
chr5:65730829 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+8415G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65730829 | |||||||
chr5:65731127 | G | A | 2 | a0007c0010t0001g0105 a0008c0012t0001g0106 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.41+8713G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731127 | |||||||
chr5:65731152 | T | G | 49 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.41+8738T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731152 | |||||||
chr5:65731177 | C | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+8763C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731177 | |||||||
chr5:65731242 | G | C | 1 | a0001c0001t0004g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.41+8828G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731242 | |||||||
chr5:65731334 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0028g0179 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.41+8920A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731334 | |||||||
chr5:65731451 | T | C | 1 | a0001c0001t0048g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41+9037T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731451 | |||||||
chr5:65731604 | C | G | 3 | a0001c0001t0052g0283 a0002c0003t0010g0267 a0002c0003t0010g0282 |
3 | HG02055.hp2 HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.41+9190C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731604 | |||||||
chr5:65731636 | A | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(53): Show |
64 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+9222A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731636 | |||||||
chr5:65731734 | TAC | T | 2 | a0001c0002t0013g0012 a0001c0002t0013g0162 |
3 | HG00609.hp2 HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.41+9322_41+9323del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731734 | ||||||
chr5:65731742 | C | CT | 41 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(38): Show |
43 | HG00323.hp2 HG00438.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.41+9354dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | ||||||
chr5:65731742 | C | CTT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0185 others(40): Show |
51 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.41+9353_41+9354dup others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | ||||||
chr5:65731742 | C | CTTT | 8 | a0001c0001t0001g0037 a0001c0001t0001g0204 a0001c0001t0002g0040 others(5): Show |
8 | HG00621.hp2 HG02027.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+9352_41+9354dup others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | ||||||
chr5:65731742 | CT | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0226 a0001c0001t0003g0067 others(3): Show |
6 | HG00099.hp2 HG01516.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+9354delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | ||||||
chr5:65731742 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0005g0046 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.41+9340_41+9354del others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65731742 | ||||||
chr5:65731747 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9333T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731747 | |||||||
chr5:65731751 | TTTTTTTT others(11): Show |
T | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+9338_41+9355del others(18): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731751 | |||||||
chr5:65731764 | TTTTTC | T | 54 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(51): Show |
55 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.41+9351_41+9355del others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731764 | |||||||
chr5:65731865 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9451G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731865 | |||||||
chr5:65731966 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9552A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65731966 | |||||||
chr5:65732148 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0028g0179 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+9734A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732148 | |||||||
chr5:65732182 | C | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+9768C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732182 | |||||||
chr5:65732256 | TAGAAAGA others(2290): Show |
T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+9859_41+12155de others(1): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65732256 | ||||||
chr5:65732351 | T | A | 1 | a0003c0005t0023g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+9937T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732351 | |||||||
chr5:65732385 | G | T | 21 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0006g0102 others(18): Show |
23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.41+9971G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732385 | |||||||
chr5:65732386 | A | T | 21 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0006g0102 others(18): Show |
23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.41+9972A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732386 | |||||||
chr5:65732645 | C | T | 1 | a0003c0005t0022g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.41+10231C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65732645 | |||||||
chr5:65733474 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(220): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.41+11060A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733474 | |||||||
chr5:65733527 | A | G | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+11113A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733527 | |||||||
chr5:65733568 | G | A | 2 | a0006c0008t0006g0103 a0006c0008t0006g0177 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.41+11154G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733568 | |||||||
chr5:65733785 | T | A | 1 | a0001c0001t0001g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.41+11371T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733785 | |||||||
chr5:65733809 | T | C | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41+11395T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733809 | |||||||
chr5:65733966 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0253 others(1): Show |
5 | HG00099.hp1 HG01123.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+11552C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733966 | |||||||
chr5:65733998 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(106): Show |
118 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.41+11584T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65733998 | |||||||
chr5:65734200 | T | C | 1 | a0001c0001t0003g0066 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.41+11786T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734200 | |||||||
chr5:65734342 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0188 |
3 | NA18999.hp2 NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.41+11928C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734342 | |||||||
chr5:65734541 | G | GA | 100 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(97): Show |
109 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.41+12140dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65734541 | ||||||
chr5:65734622 | T | A | 2 | a0001c0001t0006g0023 a0001c0001t0006g0044 |
2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.41+12208T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734622 | |||||||
chr5:65734640 | A | G | 1 | a0001c0001t0048g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41+12226A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734640 | |||||||
chr5:65734687 | C | T | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+12273C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734687 | |||||||
chr5:65734688 | G | A | 91 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(88): Show |
99 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.41+12274G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734688 | |||||||
chr5:65734742 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12328A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734742 | |||||||
chr5:65734750 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.41+12336A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734750 | |||||||
chr5:65734869 | T | G | 1 | a0003c0005t0023g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+12455T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734869 | |||||||
chr5:65734894 | C | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12480C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734894 | |||||||
chr5:65734905 | A | G | 7 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(4): Show |
8 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+12491A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65734905 | |||||||
chr5:65735000 | C | T | 1 | a0001c0002t0001g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.41+12586C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735000 | |||||||
chr5:65735117 | G | T | 1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+12703G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735117 | |||||||
chr5:65735122 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+12708T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735122 | |||||||
chr5:65735215 | TA | T | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+12803delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65735215 | ||||||
chr5:65735665 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+13251A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735665 | |||||||
chr5:65735755 | A | T | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+13341A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735755 | |||||||
chr5:65735811 | A | G | 1 | a0001c0001t0005g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.41+13397A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65735811 | |||||||
chr5:65736104 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(112): Show |
126 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.41+13690T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736104 | |||||||
chr5:65736364 | C | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+13950C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736364 | |||||||
chr5:65736527 | C | T | 1 | a0001c0001t0006g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+14113C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736527 | |||||||
chr5:65736580 | T | C | 1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+14166T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736580 | |||||||
chr5:65736640 | AT | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14229delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65736640 | ||||||
chr5:65736676 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14262G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736676 | |||||||
chr5:65736700 | G | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14286G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736700 | |||||||
chr5:65736990 | A | G | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+14576A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736990 | |||||||
chr5:65736997 | C | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14583C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65736997 | |||||||
chr5:65737154 | CTG | C | 13 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(10): Show |
13 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+14744_41+14745d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65737154 | ||||||
chr5:65737221 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14807G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737221 | |||||||
chr5:65737263 | A | G | 1 | a0001c0001t0039g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+14849A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737263 | |||||||
chr5:65737306 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+14892G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737306 | |||||||
chr5:65737311 | C | T | 13 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(10): Show |
13 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+14897C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737311 | |||||||
chr5:65737541 | A | G | 22 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(19): Show |
22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+15127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737541 | |||||||
chr5:65737627 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15213T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737627 | |||||||
chr5:65737637 | G | A | 1 | a0001c0001t0039g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+15223G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737637 | |||||||
chr5:65737739 | G | A | 22 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(19): Show |
22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+15325G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737739 | |||||||
chr5:65737755 | A | G | 1 | a0001c0001t0004g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+15341A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737755 | |||||||
chr5:65737821 | C | T | 1 | a0001c0013t0038g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+15407C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737821 | |||||||
chr5:65737881 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.41+15467G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737881 | |||||||
chr5:65737898 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15484G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737898 | |||||||
chr5:65737909 | C | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15495C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65737909 | |||||||
chr5:65738025 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+15611A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738025 | |||||||
chr5:65738043 | G | A | 1 | a0001c0001t0009g0024 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41+15629G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738043 | |||||||
chr5:65738061 | G | A | 51 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(48): Show |
52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+15647G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738061 | |||||||
chr5:65738068 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+15654G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738068 | |||||||
chr5:65738135 | GA | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(130): Show |
145 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.41+15735delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738135 | ||||||
chr5:65738312 | G | GGT | 56 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(53): Show |
64 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+15900_41+15901d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738312 | ||||||
chr5:65738487 | A | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16073A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738487 | |||||||
chr5:65738552 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16138G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738552 | |||||||
chr5:65738610 | T | C | 1 | a0001c0001t0006g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.41+16196T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738610 | |||||||
chr5:65738632 | A | T | 6 | a0002c0003t0007g0085 a0002c0003t0041g0089 a0002c0004t0016g0088 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+16218A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738632 | |||||||
chr5:65738744 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16330A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738744 | |||||||
chr5:65738904 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0002g0098 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+16490G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738904 | |||||||
chr5:65738926 | G | GTATATAT others(26): Show |
10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16513_41+16514i others(35): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | ||||||
chr5:65738926 | G | GTATATAT others(28): Show |
1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16513_41+16514i others(37): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | ||||||
chr5:65738926 | GTGTATAT others(18): Show |
G | 2 | a0002c0004t0017g0277 a0002c0004t0017g0292 |
2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16514_41+16538d others(27): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738926 | ||||||
chr5:65738928 | G | A | 56 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(53): Show |
59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.41+16514G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738928 | |||||||
chr5:65738928 | G | T | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16514G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738928 | |||||||
chr5:65738936 | A | G | 46 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(43): Show |
49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16522A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738936 | |||||||
chr5:65738937 | T | TA | 42 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(39): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16523_41+16524i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738937 | |||||||
chr5:65738937 | T | TATATATA others(17): Show |
4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16523_41+16524i others(26): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738937 | |||||||
chr5:65738938 | T | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16524T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738938 | |||||||
chr5:65738939 | T | A | 42 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(39): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16525T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738939 | |||||||
chr5:65738940 | T | TA | 10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16526_41+16527i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738940 | |||||||
chr5:65738941 | T | A | 46 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(43): Show |
49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16527T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738941 | |||||||
chr5:65738942 | T | A | 11 | a0001c0001t0052g0283 a0001c0002t0001g0115 a0002c0003t0010g0260 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16528T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738942 | |||||||
chr5:65738944 | T | A | 42 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(39): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16530T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738944 | |||||||
chr5:65738949 | G | A | 57 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(54): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.41+16535G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738949 | |||||||
chr5:65738951 | T | A | 42 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(39): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.41+16537T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738951 | |||||||
chr5:65738952 | T | TTATA | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16538_41+16539i others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738952 | |||||||
chr5:65738953 | A | AT | 39 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(36): Show |
40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16540dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738953 | ||||||
chr5:65738955 | A | AT | 3 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 |
3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+16542dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738955 | ||||||
chr5:65738961 | G | A | 11 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16547G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738961 | |||||||
chr5:65738961 | G | T | 46 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(43): Show |
49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16547G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738961 | |||||||
chr5:65738962 | T | A | 11 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+16548T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738962 | |||||||
chr5:65738970 | A | ATATATAT others(5): Show |
10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16556_41+16557i others(14): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738970 | |||||||
chr5:65738970 | A | T | 46 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(43): Show |
49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.41+16556A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738970 | |||||||
chr5:65738972 | T | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+16558T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | |||||||
chr5:65738972 | T | TTTTATA | 3 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 |
3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+16558_41+16559i others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | |||||||
chr5:65738972 | TA | T | 39 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(36): Show |
40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16559delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738972 | |||||||
chr5:65738975 | A | T | 39 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(36): Show |
40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16561A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738975 | |||||||
chr5:65738976 | TA | T | 11 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0004c0006t0001g0009 others(8): Show |
12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16563delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738976 | |||||||
chr5:65738979 | AT | A | 11 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0004c0006t0001g0009 others(8): Show |
12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16567delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738979 | ||||||
chr5:65738980 | T | A | 44 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(41): Show |
47 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.41+16566T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738980 | |||||||
chr5:65738980 | T | TAAATA | 10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16566_41+16567i others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738980 | |||||||
chr5:65738981 | T | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16567T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738981 | |||||||
chr5:65738983 | T | TA | 10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16570dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738983 | ||||||
chr5:65738986 | A | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0002g0098 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+16572A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738986 | |||||||
chr5:65738986 | A | T | 11 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0004c0006t0001g0009 others(8): Show |
12 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+16572A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738986 | |||||||
chr5:65738988 | T | A | 29 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0028 others(26): Show |
32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.41+16574T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738988 | |||||||
chr5:65738988 | T | TTA | 222 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(219): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.41+16582_41+16583d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65738988 | ||||||
chr5:65738991 | T | A | 7 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0262 others(4): Show |
9 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+16577T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738991 | |||||||
chr5:65738993 | T | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16579T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738993 | |||||||
chr5:65738997 | T | A | 10 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16583T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738997 | |||||||
chr5:65738997 | T | TAAA | 39 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(36): Show |
40 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.41+16583_41+16584i others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738997 | |||||||
chr5:65738998 | T | A | 12 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0262 others(9): Show |
16 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.41+16584T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738998 | |||||||
chr5:65738999 | T | A | 56 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(53): Show |
59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.41+16585T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65738999 | |||||||
chr5:65739000 | T | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41+16586T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739000 | |||||||
chr5:65739003 | A | AT | 8 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0262 others(5): Show |
10 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16589_41+16590i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739003 | |||||||
chr5:65739008 | AT | A | 7 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0262 others(4): Show |
9 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+16595delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739008 | |||||||
chr5:65739009 | T | TATAAAAT others(50): Show |
2 | a0001c0001t0004g0302 a0001c0001t0055g0304 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41+16597_41+16598i others(59): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | ||||||
chr5:65739009 | T | TATAAAAT others(52): Show |
35 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(32): Show |
36 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+16597_41+16598i others(61): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | ||||||
chr5:65739009 | T | TATATAAA | 10 | a0001c0001t0048g0264 a0002c0003t0010g0260 a0002c0003t0010g0267 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+16597_41+16598i others(9): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739009 | ||||||
chr5:65739011 | T | A | 8 | a0001c0001t0002g0257 a0001c0001t0005g0261 a0001c0001t0006g0262 others(5): Show |
10 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+16597T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739011 | |||||||
chr5:65739012 | T | A | 57 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(54): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.41+16598T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739012 | |||||||
chr5:65739023 | A | T | 2 | a0002c0004t0017g0277 a0002c0004t0017g0292 |
2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16609A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739023 | |||||||
chr5:65739032 | TATATATA others(6): Show |
T | 2 | a0002c0004t0017g0277 a0002c0004t0017g0292 |
2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.41+16630_41+16642d others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65739032 | ||||||
chr5:65739042 | A | T | 58 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(55): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.41+16628A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739042 | |||||||
chr5:65739045 | A | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16631A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739045 | |||||||
chr5:65739109 | G | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+16695G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739109 | |||||||
chr5:65739185 | G | A | 51 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(48): Show |
52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.41+16771G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739185 | |||||||
chr5:65739321 | G | A | 1 | a0003c0005t0020g0018 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41+16907G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739321 | |||||||
chr5:65739432 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.41+17018G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739432 | |||||||
chr5:65739484 | T | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+17070T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739484 | |||||||
chr5:65739601 | T | G | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41+17187T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739601 | |||||||
chr5:65739880 | C | T | 8 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(5): Show |
9 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+17466C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65739880 | |||||||
chr5:65740068 | C | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0002g0098 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+17654C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740068 | |||||||
chr5:65740082 | T | C | 1 | a0006c0008t0006g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41+17668T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740082 | |||||||
chr5:65740092 | C | G | 4 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(1): Show |
4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+17678C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740092 | |||||||
chr5:65740472 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+18058A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740472 | |||||||
chr5:65740601 | G | C | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-17966G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740601 | |||||||
chr5:65740757 | A | G | 1 | a0001c0001t0005g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.42-17810A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740757 | |||||||
chr5:65740813 | T | TTA | 76 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(73): Show |
85 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.42-17742_42-17741d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740813 | ||||||
chr5:65740813 | T | TTATA | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-17744_42-17741d others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740813 | ||||||
chr5:65740870 | CT | C | 6 | a0001c0001t0003g0066 a0001c0001t0036g0026 a0004c0006t0001g0101 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-17679delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740870 | ||||||
chr5:65740870 | CTT | C | 57 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(54): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.42-17680_42-17679d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65740870 | ||||||
chr5:65740934 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42-17633C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740934 | |||||||
chr5:65740976 | C | A | 1 | a0003c0005t0022g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.42-17591C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65740976 | |||||||
chr5:65741135 | G | A | 1 | a0001c0002t0001g0010 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.42-17432G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741135 | |||||||
chr5:65741192 | G | C | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-17375G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741192 | |||||||
chr5:65741389 | C | T | 1 | a0001c0001t0014g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.42-17178C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741389 | |||||||
chr5:65741436 | T | C | 1 | a0001c0001t0006g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-17131T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741436 | |||||||
chr5:65741459 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-17108A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741459 | |||||||
chr5:65741624 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
92 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.42-16943C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741624 | |||||||
chr5:65741852 | A | G | 2 | a0002c0004t0017g0277 a0002c0004t0017g0292 |
2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42-16715A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65741852 | |||||||
chr5:65742013 | T | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16554T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742013 | |||||||
chr5:65742179 | T | C | 92 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(89): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.42-16388T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742179 | |||||||
chr5:65742223 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-16344G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742223 | |||||||
chr5:65742244 | AAG | A | 3 | a0001c0001t0015g0043 a0001c0001t0015g0249 a0001c0001t0015g0250 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.42-16320_42-16319d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65742244 | ||||||
chr5:65742269 | TAA | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16297_42-16296d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742269 | |||||||
chr5:65742284 | G | A | 3 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 |
3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-16283G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742284 | |||||||
chr5:65742314 | G | A | 92 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(89): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.42-16253G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742314 | |||||||
chr5:65742380 | A | G | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-16187A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742380 | |||||||
chr5:65742404 | C | T | 304 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(301): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.42-16163C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742404 | |||||||
chr5:65742504 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-16063G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742504 | |||||||
chr5:65742548 | C | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-16019C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742548 | |||||||
chr5:65742627 | T | A | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-15940T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742627 | |||||||
chr5:65742654 | G | A | 1 | a0001c0002t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.42-15913G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742654 | |||||||
chr5:65742698 | A | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-15869A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742698 | |||||||
chr5:65742737 | G | A | 63 | a0001c0001t0002g0017 a0001c0001t0002g0198 a0001c0001t0002g0199 others(60): Show |
67 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.42-15830G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742737 | |||||||
chr5:65742850 | C | G | 2 | a0001c0001t0006g0049 a0001c0001t0024g0045 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.42-15717C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742850 | |||||||
chr5:65742902 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42-15665C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742902 | |||||||
chr5:65742928 | G | A | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-15639G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65742928 | |||||||
chr5:65743000 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-15567A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743000 | |||||||
chr5:65743156 | T | TGCTGGTA others(2): Show |
4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0002c0003t0007g0228 others(1): Show |
4 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-15407_42-15399d others(11): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65743156 | ||||||
chr5:65743223 | TCAA | T | 4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0002c0003t0007g0228 others(1): Show |
4 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-15340_42-15338d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65743223 | ||||||
chr5:65743572 | G | A | 49 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-14995G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743572 | |||||||
chr5:65743605 | G | T | 2 | a0001c0001t0027g0307 a0001c0001t0027g0308 |
2 | NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-14962G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743605 | |||||||
chr5:65743779 | A | C | 9 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-14788A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743779 | |||||||
chr5:65743783 | C | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-14784C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743783 | |||||||
chr5:65743840 | G | T | 55 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(52): Show |
58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.42-14727G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743840 | |||||||
chr5:65743891 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.42-14676G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743891 | |||||||
chr5:65743948 | C | T | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-14619C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65743948 | |||||||
chr5:65744053 | G | T | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14514G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744053 | |||||||
chr5:65744138 | C | CT | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14428dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744138 | ||||||
chr5:65744162 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0163 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.42-14405G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744162 | |||||||
chr5:65744171 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42-14396A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744171 | |||||||
chr5:65744415 | G | T | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-14152G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744415 | |||||||
chr5:65744440 | A | G | 59 | a0001c0001t0002g0257 a0001c0001t0004g0265 a0001c0001t0004g0270 others(56): Show |
62 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-14127A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744440 | |||||||
chr5:65744472 | C | CT | 8 | a0001c0001t0001g0161 a0001c0001t0002g0148 a0001c0001t0003g0066 others(5): Show |
8 | HG01243.hp1 HG03041.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-14079dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | ||||||
chr5:65744472 | C | CTTT | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-14081_42-14079d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | ||||||
chr5:65744472 | CT | C | 62 | a0001c0001t0002g0251 a0001c0001t0004g0265 a0001c0001t0004g0270 others(59): Show |
64 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.42-14079delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744472 | ||||||
chr5:65744473 | T | C | 4 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(1): Show |
4 | HG00741.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-14094T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744473 | |||||||
chr5:65744474 | T | C | 2 | a0001c0001t0026g0278 a0001c0001t0026g0294 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-14093T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744474 | |||||||
chr5:65744489 | G | T | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-14078G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744489 | |||||||
chr5:65744618 | G | A | 51 | a0001c0001t0004g0265 a0001c0001t0004g0270 a0001c0001t0004g0271 others(48): Show |
52 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.42-13949G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744618 | |||||||
chr5:65744647 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.42-13920C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744647 | |||||||
chr5:65744834 | C | T | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-13733C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65744834 | |||||||
chr5:65744883 | G | GAGAAA | 64 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0002g0225 others(61): Show |
65 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.42-13674_42-13670d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65744883 | ||||||
chr5:65745047 | G | A | 1 | a0001c0001t0004g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.42-13520G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745047 | |||||||
chr5:65745110 | C | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(104): Show |
116 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.42-13457C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745110 | |||||||
chr5:65745143 | C | T | 1 | a0001c0001t0006g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-13424C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745143 | |||||||
chr5:65745247 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.42-13320A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745247 | |||||||
chr5:65745690 | G | A | 2 | a0001c0001t0001g0037 a0001c0015t0004g0263 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.42-12877G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745690 | |||||||
chr5:65745824 | T | C | 1 | a0001c0007t0018g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.42-12743T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745824 | |||||||
chr5:65745858 | C | T | 3 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 |
3 | NA18948.hp1 NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.42-12709C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745858 | |||||||
chr5:65745869 | G | A | 22 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(19): Show |
22 | HG01516.hp2 HG01517.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-12698G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745869 | |||||||
chr5:65745922 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(150): Show |
165 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.42-12645A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745922 | |||||||
chr5:65745963 | G | A | 3 | a0001c0001t0004g0293 a0001c0001t0004g0295 a0001c0001t0056g0259 |
3 | HG03688.hp1 NA18973.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.42-12604G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65745963 | |||||||
chr5:65746141 | G | A | 1 | a0005c0009t0035g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42-12426G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746141 | |||||||
chr5:65746211 | G | A | 1 | a0003c0005t0020g0018 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.42-12356G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746211 | |||||||
chr5:65746248 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.42-12319A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746248 | |||||||
chr5:65746304 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0005g0230 |
2 | NA18994.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.42-12263T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746304 | |||||||
chr5:65746420 | G | C | 1 | a0001c0001t0006g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-12147G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746420 | |||||||
chr5:65746497 | A | G | 2 | a0001c0001t0006g0028 a0001c0001t0031g0254 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.42-12070A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746497 | |||||||
chr5:65746637 | T | C | 1 | a0002c0004t0007g0244 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42-11930T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746637 | |||||||
chr5:65746990 | C | T | 5 | a0001c0001t0002g0196 a0001c0002t0001g0016 a0001c0002t0001g0184 others(2): Show |
6 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-11577C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746990 | |||||||
chr5:65746991 | G | A | 3 | a0001c0001t0004g0270 a0001c0001t0004g0271 a0001c0001t0004g0290 |
3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.42-11576G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65746991 | |||||||
chr5:65747042 | A | G | 4 | a0004c0006t0001g0009 a0004c0006t0001g0101 a0004c0006t0001g0107 others(1): Show |
5 | HG02451.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-11525A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747042 | |||||||
chr5:65747192 | T | C | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-11375T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747192 | |||||||
chr5:65747200 | AT | A | 4 | a0004c0006t0001g0009 a0004c0006t0001g0101 a0004c0006t0001g0107 others(1): Show |
5 | HG02451.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-11364delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65747200 | ||||||
chr5:65747266 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0195 |
2 | NA20805.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.42-11301C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747266 | |||||||
chr5:65747534 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.42-11033T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65747534 | |||||||
chr5:65748036 | A | G | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-10531A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748036 | |||||||
chr5:65748073 | C | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-10494C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748073 | |||||||
chr5:65748100 | C | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-10467C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748100 | |||||||
chr5:65748235 | C | T | 7 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0003g0055 others(4): Show |
7 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-10332C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748235 | |||||||
chr5:65748381 | T | C | 1 | a0002c0004t0017g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.42-10186T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748381 | |||||||
chr5:65748495 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.42-10072C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748495 | |||||||
chr5:65748637 | C | G | 1 | a0001c0001t0025g0020 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.42-9930C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748637 | |||||||
chr5:65748695 | A | G | 1 | a0001c0001t0004g0300 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.42-9872A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748695 | |||||||
chr5:65748782 | A | G | 2 | a0001c0001t0006g0102 a0001c0001t0006g0110 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.42-9785A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748782 | |||||||
chr5:65748902 | A | T | 1 | a0001c0002t0001g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.42-9665A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65748902 | |||||||
chr5:65749144 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(138): Show |
153 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.42-9423G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749144 | |||||||
chr5:65749245 | A | C | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-9322A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749245 | |||||||
chr5:65749284 | A | G | 1 | a0001c0001t0011g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.42-9283A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749284 | |||||||
chr5:65749375 | G | C | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-9192G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65749375 | |||||||
chr5:65750152 | G | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-8415G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750152 | |||||||
chr5:65750175 | G | A | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.42-8392G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750175 | |||||||
chr5:65750223 | G | C | 2 | a0004c0006t0001g0009 a0004c0006t0001g0107 |
3 | NA19030.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.42-8344G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750223 | |||||||
chr5:65750259 | T | A | 4 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-8308T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750259 | |||||||
chr5:65750408 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0009g0116 |
2 | HG01975.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.42-8159G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750408 | |||||||
chr5:65750445 | A | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(110): Show |
122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.42-8122A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750445 | |||||||
chr5:65750860 | A | C | 2 | a0001c0001t0004g0281 a0001c0001t0053g0299 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.42-7707A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750860 | |||||||
chr5:65750986 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(164): Show |
179 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.42-7581G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65750986 | |||||||
chr5:65751025 | A | C | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-7542A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751025 | |||||||
chr5:65751061 | G | A | 6 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0003g0055 others(3): Show |
6 | HG01081.hp2 HG01255.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-7506G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751061 | |||||||
chr5:65751124 | CA | C | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-7440delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65751124 | ||||||
chr5:65751218 | A | G | 2 | a0001c0001t0026g0278 a0001c0001t0026g0294 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-7349A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751218 | |||||||
chr5:65751299 | A | G | 1 | a0001c0001t0006g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-7268A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751299 | |||||||
chr5:65751418 | A | G | 1 | a0001c0001t0005g0233 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.42-7149A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751418 | |||||||
chr5:65751630 | G | A | 49 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-6937G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751630 | |||||||
chr5:65751722 | C | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(110): Show |
122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.42-6845C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751722 | |||||||
chr5:65751841 | T | TATG | 3 | a0001c0001t0002g0257 a0002c0004t0043g0258 a0002c0016t0034g0256 |
3 | HG02257.hp1 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-6714_42-6712dup others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65751841 | ||||||
chr5:65751856 | A | G | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-6711A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751856 | |||||||
chr5:65751912 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-6655C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751912 | |||||||
chr5:65751913 | G | A | 1 | a0001c0002t0001g0117 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.42-6654G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65751913 | |||||||
chr5:65752010 | T | C | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-6557T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752010 | |||||||
chr5:65752115 | A | G | 1 | a0001c0002t0004g0287 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.42-6452A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752115 | |||||||
chr5:65752137 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(114): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-6430T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752137 | |||||||
chr5:65752237 | CA | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-6317delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65752237 | ||||||
chr5:65752510 | G | A | 1 | a0001c0001t0009g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42-6057G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752510 | |||||||
chr5:65752554 | T | G | 1 | a0001c0002t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.42-6013T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752554 | |||||||
chr5:65752660 | T | C | 49 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-5907T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752660 | |||||||
chr5:65752706 | C | T | 1 | a0001c0002t0001g0182 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.42-5861C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752706 | |||||||
chr5:65752800 | G | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-5767G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752800 | |||||||
chr5:65752901 | T | G | 4 | a0001c0002t0001g0003 a0001c0002t0001g0147 a0001c0002t0001g0165 others(1): Show |
5 | HG00323.hp1 HG00621.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-5666T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65752901 | |||||||
chr5:65753052 | C | T | 75 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0216 others(72): Show |
76 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.42-5515C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753052 | |||||||
chr5:65753107 | A | G | 3 | a0001c0001t0051g0298 a0002c0004t0017g0277 a0002c0004t0017g0292 |
3 | HG01167.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42-5460A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753107 | |||||||
chr5:65753187 | T | A | 1 | a0001c0002t0001g0119 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.42-5380T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753187 | |||||||
chr5:65753200 | G | T | 8 | a0002c0003t0007g0085 a0002c0003t0041g0089 a0002c0004t0016g0061 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-5367G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753200 | |||||||
chr5:65753207 | A | G | 1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-5360A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753207 | |||||||
chr5:65753317 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-5250A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753317 | |||||||
chr5:65753497 | A | G | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.42-5070A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753497 | |||||||
chr5:65753539 | C | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(280): Show |
304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.42-5028C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753539 | |||||||
chr5:65753564 | C | T | 49 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-5003C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753564 | |||||||
chr5:65753650 | C | CA | 23 | a0001c0001t0001g0120 a0001c0001t0001g0185 a0001c0001t0002g0040 others(20): Show |
25 | HG01074.hp2 HG01109.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.42-4902dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65753650 | ||||||
chr5:65753765 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.42-4802T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753765 | |||||||
chr5:65753837 | C | G | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4730C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65753837 | |||||||
chr5:65754204 | C | T | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4363C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754204 | |||||||
chr5:65754225 | T | C | 15 | a0001c0001t0005g0122 a0001c0001t0005g0164 a0001c0002t0001g0011 others(12): Show |
16 | NA18941.hp2 NA18955.hp1 NA18961.hp1 others(13): Show |
intron_variant | MODIFIER | c.42-4342T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754225 | |||||||
chr5:65754255 | AG | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-4311delG | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754255 | |||||||
chr5:65754307 | C | G | 1 | a0001c0002t0001g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.42-4260C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754307 | |||||||
chr5:65754371 | C | T | 8 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(5): Show |
9 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-4196C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754371 | |||||||
chr5:65754419 | G | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(122): Show |
136 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.42-4148G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754419 | |||||||
chr5:65754564 | A | G | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0154 |
3 | NA18953.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.42-4003A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754564 | |||||||
chr5:65754608 | T | G | 1 | a0001c0001t0039g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42-3959T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754608 | |||||||
chr5:65754620 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42-3947C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754620 | |||||||
chr5:65754639 | C | T | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-3928C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754639 | |||||||
chr5:65754680 | C | A | 3 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0004g0275 |
3 | NA18948.hp1 NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.42-3887C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754680 | |||||||
chr5:65754718 | A | G | 4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0002c0003t0007g0228 others(1): Show |
4 | HG01256.hp1 HG01952.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3849A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754718 | |||||||
chr5:65754743 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(52): Show |
63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.42-3824C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754743 | |||||||
chr5:65754808 | A | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0170 |
3 | NA18949.hp1 NA18992.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.42-3759A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65754808 | |||||||
chr5:65755065 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-3502C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755065 | |||||||
chr5:65755378 | T | C | 1 | a0002c0003t0007g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.42-3189T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755378 | |||||||
chr5:65755677 | ATTAG | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-2885_42-2882del others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65755677 | ||||||
chr5:65755764 | A | G | 1 | a0002c0004t0007g0245 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-2803A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755764 | |||||||
chr5:65755829 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(114): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-2738G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755829 | |||||||
chr5:65755928 | T | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(114): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.42-2639T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755928 | |||||||
chr5:65755977 | G | A | 19 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0005g0052 others(16): Show |
24 | HG00609.hp2 HG01258.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.42-2590G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65755977 | |||||||
chr5:65756030 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.42-2537A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756030 | |||||||
chr5:65756188 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.42-2379A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756188 | |||||||
chr5:65756229 | C | G | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-2338C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756229 | |||||||
chr5:65756390 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.42-2177A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756390 | |||||||
chr5:65756604 | A | G | 2 | a0001c0001t0021g0097 a0001c0001t0030g0059 |
2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.42-1963A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65756604 | |||||||
chr5:65757032 | A | G | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 |
3 | NA18941.hp2 NA18955.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.42-1535A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757032 | |||||||
chr5:65757390 | G | A | 25 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0002g0098 others(22): Show |
26 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.42-1177G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757390 | |||||||
chr5:65757541 | A | G | 1 | a0003c0005t0023g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.42-1026A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757541 | |||||||
chr5:65757573 | G | T | 1 | a0001c0011t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42-994G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757573 | |||||||
chr5:65757596 | T | TTA | 49 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-963_42-962dupAT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 65757596 | ||||||
chr5:65757662 | G | C | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-905G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757662 | |||||||
chr5:65757696 | A | G | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.42-871A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757696 | |||||||
chr5:65757918 | G | C | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-649G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757918 | |||||||
chr5:65757926 | A | G | 49 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(46): Show |
50 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-641A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65757926 | |||||||
chr5:65758102 | G | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-465G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758102 | |||||||
chr5:65758209 | G | A | 2 | a0007c0010t0001g0105 a0008c0012t0001g0106 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.42-358G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758209 | |||||||
chr5:65758247 | G | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-320G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758247 | |||||||
chr5:65758298 | A | T | 1 | a0001c0002t0001g0031 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.42-269A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758298 | |||||||
chr5:65758321 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(52): Show |
63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.42-246A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758321 | |||||||
chr5:65758424 | A | G | 3 | a0001c0001t0004g0301 a0001c0001t0027g0307 a0001c0001t0027g0308 |
3 | NA18988.hp1 NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-143A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758424 | |||||||
chr5:65758556 | A | G | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-11A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 1/12 | chr5 | 65758556 | |||||||
chr5:65758984 | A | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(134): Show |
149 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.301+158A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65758984 | |||||||
chr5:65758997 | A | G | 1 | a0001c0002t0001g0211 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.301+171A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65758997 | |||||||
chr5:65759309 | G | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+483G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759309 | |||||||
chr5:65759396 | GTGTC | G | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+574_301+577del others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65759396 | ||||||
chr5:65759400 | CTG | C | 159 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(156): Show |
169 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.301+590_301+591del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65759400 | ||||||
chr5:65759491 | T | C | 2 | a0001c0001t0026g0278 a0001c0001t0026g0294 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.301+665T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759491 | |||||||
chr5:65759543 | G | A | 1 | a0001c0001t0047g0247 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.301+717G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65759543 | |||||||
chr5:65760270 | C | A | 2 | a0001c0007t0018g0291 a0001c0007t0018g0303 |
2 | HG00438.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.301+1444C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760270 | |||||||
chr5:65760368 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1542T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760368 | |||||||
chr5:65760371 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1545A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760371 | |||||||
chr5:65760372 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1546A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760372 | |||||||
chr5:65760373 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1547G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760373 | |||||||
chr5:65760384 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1558A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760384 | |||||||
chr5:65760385 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1559G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760385 | |||||||
chr5:65760386 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1560A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760386 | |||||||
chr5:65760390 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1564A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760390 | |||||||
chr5:65760395 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1569C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760395 | |||||||
chr5:65760397 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1571A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760397 | |||||||
chr5:65760403 | T | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1577T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760403 | |||||||
chr5:65760404 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1578A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760404 | |||||||
chr5:65760406 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1580A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760406 | |||||||
chr5:65760407 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1581G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760407 | |||||||
chr5:65760409 | T | A | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1583T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760409 | |||||||
chr5:65760410 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1584T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760410 | |||||||
chr5:65760419 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1593G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760419 | |||||||
chr5:65760420 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1594G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760420 | |||||||
chr5:65760423 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1597A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760423 | |||||||
chr5:65760428 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1602A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760428 | |||||||
chr5:65760430 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1604G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760430 | |||||||
chr5:65760432 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1606G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760432 | |||||||
chr5:65760434 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1608G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760434 | |||||||
chr5:65760440 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1614C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760440 | |||||||
chr5:65760441 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1615A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760441 | |||||||
chr5:65760443 | C | A | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1617C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760443 | |||||||
chr5:65760446 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1620G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760446 | |||||||
chr5:65760447 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1621G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760447 | |||||||
chr5:65760454 | T | G | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1628T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760454 | |||||||
chr5:65760455 | T | A | 1 | a0001c0001t0002g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.301+1629T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760455 | |||||||
chr5:65760814 | A | G | 6 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0001c0001t0005g0046 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+1988A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65760814 | |||||||
chr5:65761291 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302-1669A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761291 | |||||||
chr5:65761448 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.302-1512G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761448 | |||||||
chr5:65761536 | C | T | 2 | a0001c0001t0005g0261 a0001c0001t0019g0019 |
3 | HG01109.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.302-1424C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761536 | |||||||
chr5:65761816 | A | G | 92 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(89): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.302-1144A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761816 | |||||||
chr5:65761841 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(52): Show |
63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.302-1119G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65761841 | |||||||
chr5:65762000 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.302-960C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762000 | |||||||
chr5:65762108 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.302-852T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762108 | |||||||
chr5:65762532 | A | G | 1 | a0001c0001t0036g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.302-428A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762532 | |||||||
chr5:65762623 | AG | A | 8 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(5): Show |
9 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-336delG | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | chr5 | 65762623 | |||||||
chr5:65762702 | C | CA | 107 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(104): Show |
116 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.302-244dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 65762702 | ||||||
chr5:65763153 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.450+45A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763153 | |||||||
chr5:65763272 | G | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+164G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763272 | |||||||
chr5:65763282 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.450+174T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763282 | |||||||
chr5:65763385 | A | G | 1 | a0001c0002t0004g0287 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.450+277A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763385 | |||||||
chr5:65763706 | T | G | 2 | a0002c0004t0016g0061 a0002c0004t0016g0063 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.450+598T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763706 | |||||||
chr5:65763744 | TA | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+637delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763744 | |||||||
chr5:65763746 | C | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+638C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763746 | |||||||
chr5:65763767 | G | A | 3 | a0001c0001t0004g0293 a0001c0001t0004g0295 a0001c0001t0056g0259 |
3 | HG03688.hp1 NA18973.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.450+659G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763767 | |||||||
chr5:65763827 | T | C | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+719T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65763827 | |||||||
chr5:65764026 | T | G | 2 | a0007c0010t0001g0105 a0008c0012t0001g0106 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450+918T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764026 | |||||||
chr5:65764118 | A | G | 1 | a0001c0002t0012g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.450+1010A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764118 | |||||||
chr5:65764259 | C | CA | 12 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0003c0005t0022g0084 others(9): Show |
13 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+1153dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65764259 | ||||||
chr5:65764285 | C | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+1177C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764285 | |||||||
chr5:65764644 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0194 a0001c0001t0001g0204 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1536C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764644 | |||||||
chr5:65764685 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.450+1577G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764685 | |||||||
chr5:65764913 | T | A | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.450+1805T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65764913 | |||||||
chr5:65765074 | G | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0161 a0001c0001t0014g0130 others(3): Show |
6 | HG02056.hp1 NA18983.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1966G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765074 | |||||||
chr5:65765274 | T | A | 1 | a0001c0001t0002g0015 | 2 | NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.450+2166T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765274 | |||||||
chr5:65765349 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+2241C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765349 | |||||||
chr5:65765454 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+2346G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765454 | |||||||
chr5:65765458 | C | T | 1 | a0001c0001t0048g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.450+2350C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765458 | |||||||
chr5:65765506 | A | G | 1 | a0003c0005t0022g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450+2398A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765506 | |||||||
chr5:65765578 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+2470A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765578 | |||||||
chr5:65765631 | C | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+2523C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765631 | |||||||
chr5:65765678 | C | G | 6 | a0001c0001t0009g0024 a0001c0001t0009g0027 a0001c0001t0009g0068 others(3): Show |
6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+2570C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765678 | |||||||
chr5:65765706 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.450+2598C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765706 | |||||||
chr5:65765966 | C | T | 2 | a0007c0010t0001g0105 a0008c0012t0001g0106 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450+2858C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65765966 | |||||||
chr5:65766004 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+2896A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766004 | |||||||
chr5:65766041 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+2933G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766041 | |||||||
chr5:65766088 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+2980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766088 | |||||||
chr5:65766513 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(52): Show |
63 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.450+3405G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766513 | |||||||
chr5:65766801 | T | C | 1 | a0001c0001t0004g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.450+3693T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65766801 | |||||||
chr5:65767015 | G | T | 48 | a0001c0001t0001g0037 a0001c0001t0004g0265 a0001c0001t0004g0270 others(45): Show |
49 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.450+3907G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767015 | |||||||
chr5:65767349 | G | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.450+4241G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767349 | |||||||
chr5:65767362 | G | A | 4 | a0001c0001t0001g0120 a0001c0002t0013g0012 a0001c0002t0013g0128 others(1): Show |
5 | HG00609.hp2 HG02027.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+4254G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767362 | |||||||
chr5:65767508 | G | C | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+4400G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767508 | |||||||
chr5:65767641 | T | G | 2 | a0002c0004t0016g0061 a0002c0004t0016g0063 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.450+4533T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767641 | |||||||
chr5:65767898 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.450+4790G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65767898 | |||||||
chr5:65768035 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+4927A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768035 | |||||||
chr5:65768196 | C | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(108): Show |
122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.450+5088C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768196 | |||||||
chr5:65768277 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+5169G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768277 | |||||||
chr5:65768412 | C | G | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+5304C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768412 | |||||||
chr5:65768462 | C | A | 2 | a0002c0004t0016g0088 a0003c0005t0021g0086 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.450+5354C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768462 | |||||||
chr5:65768757 | C | T | 1 | a0001c0001t0007g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.450+5649C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768757 | |||||||
chr5:65768784 | C | T | 2 | a0001c0001t0032g0220 a0001c0001t0033g0218 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.450+5676C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768784 | |||||||
chr5:65768914 | C | T | 1 | a0001c0002t0001g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.450+5806C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65768914 | |||||||
chr5:65769118 | T | G | 2 | a0002c0004t0017g0277 a0002c0004t0017g0292 |
2 | HG01167.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.450+6010T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769118 | |||||||
chr5:65769201 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+6093A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769201 | |||||||
chr5:65769332 | C | G | 6 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0193 others(3): Show |
6 | HG00323.hp2 HG02257.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+6224C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769332 | |||||||
chr5:65769404 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.450+6296G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769404 | |||||||
chr5:65769547 | T | A | 1 | a0001c0001t0004g0281 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.450+6439T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769547 | |||||||
chr5:65769582 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+6474T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769582 | |||||||
chr5:65769624 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(160): Show |
175 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.450+6516G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769624 | |||||||
chr5:65769666 | A | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.450+6558A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769666 | |||||||
chr5:65769724 | A | G | 188 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(185): Show |
201 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.450+6616A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769724 | |||||||
chr5:65769725 | T | G | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+6617T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769725 | |||||||
chr5:65769907 | C | T | 1 | a0001c0001t0003g0079 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.450+6799C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65769907 | |||||||
chr5:65770163 | C | T | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.450+7055C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770163 | |||||||
chr5:65770278 | A | T | 1 | a0001c0001t0003g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.451-7149A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770278 | |||||||
chr5:65770498 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-6929A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770498 | |||||||
chr5:65770519 | G | T | 1 | a0001c0002t0001g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.451-6908G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770519 | |||||||
chr5:65770656 | C | T | 3 | a0001c0001t0002g0143 a0001c0002t0001g0111 a0001c0002t0001g0157 |
3 | HG01981.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.451-6771C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770656 | |||||||
chr5:65770659 | C | T | 1 | a0001c0001t0053g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-6768C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770659 | |||||||
chr5:65770680 | A | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0194 a0001c0001t0001g0204 |
3 | HG00323.hp2 HG02257.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.451-6747A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770680 | |||||||
chr5:65770764 | T | A | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-6663T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770764 | |||||||
chr5:65770915 | G | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-6512G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65770915 | |||||||
chr5:65771046 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0028g0179 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.451-6381C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771046 | |||||||
chr5:65771214 | A | G | 92 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0114 others(89): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.451-6213A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771214 | |||||||
chr5:65771683 | C | T | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-5744C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771683 | |||||||
chr5:65771923 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-5504A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65771923 | |||||||
chr5:65771963 | C | CA | 39 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0002g0223 others(36): Show |
39 | HG00741.hp2 HG01070.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.451-5450dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | ||||||
chr5:65771963 | C | CAA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0239 a0001c0001t0001g0240 others(16): Show |
22 | HG01109.hp1 HG01243.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.451-5451_451-5450d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | ||||||
chr5:65771963 | C | CAAA | 16 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0193 others(13): Show |
18 | HG00323.hp2 HG01081.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-5452_451-5450d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | ||||||
chr5:65771963 | C | CAAAA | 87 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(84): Show |
93 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.451-5453_451-5450d others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | ||||||
chr5:65771963 | C | CAAAAA | 9 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0004g0274 others(6): Show |
10 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-5454_451-5450d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65771963 | ||||||
chr5:65772094 | T | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0188 |
3 | NA18999.hp2 NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.451-5333T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772094 | |||||||
chr5:65772220 | A | C | 169 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(166): Show |
181 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.451-5207A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772220 | |||||||
chr5:65772451 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-4976G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772451 | |||||||
chr5:65772451 | G | C | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.451-4976G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772451 | |||||||
chr5:65772879 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-4548C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772879 | |||||||
chr5:65772891 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.451-4536C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772891 | |||||||
chr5:65772898 | A | G | 1 | a0001c0001t0005g0232 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.451-4529A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65772898 | |||||||
chr5:65772953 | GT | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
173 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.451-4460delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65772953 | ||||||
chr5:65773127 | A | AT | 167 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(164): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.451-4280dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65773127 | ||||||
chr5:65773255 | C | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-4172C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773255 | |||||||
chr5:65773592 | GAAGAAA | G | 8 | a0002c0003t0007g0085 a0002c0003t0041g0089 a0002c0004t0016g0061 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3830_451-3825d others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65773592 | ||||||
chr5:65773616 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.451-3811C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773616 | |||||||
chr5:65773797 | G | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451-3630G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65773797 | |||||||
chr5:65774043 | A | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-3384A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774043 | |||||||
chr5:65774055 | G | GT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0180 others(51): Show |
62 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.451-3356dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | ||||||
chr5:65774055 | G | GTT | 78 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(75): Show |
82 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.451-3357_451-3356d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | ||||||
chr5:65774055 | G | GTTT | 36 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(33): Show |
36 | HG00741.hp2 HG01256.hp1 HG01516.hp2 others(33): Show |
intron_variant | MODIFIER | c.451-3358_451-3356d others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774055 | ||||||
chr5:65774147 | G | GT | 4 | a0001c0001t0002g0017 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
5 | HG01496.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-3279dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774147 | ||||||
chr5:65774468 | T | C | 1 | a0002c0003t0049g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.451-2959T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774468 | |||||||
chr5:65774573 | C | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(107): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.451-2854C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774573 | |||||||
chr5:65774580 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-2847A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774580 | |||||||
chr5:65774647 | T | C | 1 | a0001c0001t0014g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.451-2780T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774647 | |||||||
chr5:65774715 | T | TTA | 7 | a0001c0001t0001g0178 a0001c0001t0002g0152 a0001c0001t0028g0179 others(4): Show |
7 | HG01261.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-2698_451-2697d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774715 | ||||||
chr5:65774729 | AT | A | 13 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0002g0098 others(10): Show |
13 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-2683delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774729 | ||||||
chr5:65774729 | ATT | A | 11 | a0001c0001t0005g0261 a0001c0001t0006g0102 a0001c0001t0006g0104 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-2684_451-2683d others(4): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 65774729 | ||||||
chr5:65774730 | T | TA | 65 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0156 others(62): Show |
72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(3): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | |||||||
chr5:65774730 | T | TATA | 41 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(38): Show |
44 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | |||||||
chr5:65774730 | T | TATATA | 11 | a0001c0001t0052g0283 a0002c0003t0010g0260 a0002c0003t0010g0267 others(8): Show |
11 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-2697_451-2696i others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774730 | |||||||
chr5:65774731 | T | A | 167 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0057 others(164): Show |
177 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-2696T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774731 | |||||||
chr5:65774732 | T | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(120): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.451-2695T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774732 | |||||||
chr5:65774733 | T | A | 131 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0057 others(128): Show |
138 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.451-2694T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774733 | |||||||
chr5:65774734 | T | A | 70 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(67): Show |
74 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.451-2693T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774734 | |||||||
chr5:65774735 | T | A | 6 | a0001c0001t0002g0246 a0001c0001t0002g0257 a0001c0002t0001g0213 others(3): Show |
6 | HG00738.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-2692T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774735 | |||||||
chr5:65774736 | T | A | 6 | a0001c0001t0004g0270 a0001c0001t0004g0271 a0001c0001t0004g0290 others(3): Show |
6 | HG01106.hp1 HG01167.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-2691T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774736 | |||||||
chr5:65774761 | G | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(111): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.451-2666G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774761 | |||||||
chr5:65774782 | T | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0120 others(87): Show |
98 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.451-2645T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774782 | |||||||
chr5:65774945 | G | A | 2 | a0001c0001t0026g0278 a0001c0001t0026g0294 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.451-2482G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774945 | |||||||
chr5:65774968 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-2459G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774968 | |||||||
chr5:65774976 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-2451C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774976 | |||||||
chr5:65774977 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.451-2450G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65774977 | |||||||
chr5:65775017 | C | G | 2 | a0001c0001t0004g0276 a0001c0001t0004g0296 |
2 | HG00733.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.451-2410C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775017 | |||||||
chr5:65775167 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.451-2260A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775167 | |||||||
chr5:65775291 | G | A | 1 | a0001c0001t0005g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.451-2136G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775291 | |||||||
chr5:65775306 | T | G | 1 | a0003c0005t0022g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.451-2121T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775306 | |||||||
chr5:65775355 | G | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-2072G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775355 | |||||||
chr5:65775446 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0184 a0001c0002t0001g0197 |
4 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1981C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775446 | |||||||
chr5:65775447 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-1980G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775447 | |||||||
chr5:65775467 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0028g0179 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.451-1960A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775467 | |||||||
chr5:65775556 | T | C | 6 | a0001c0001t0009g0024 a0001c0001t0009g0027 a0001c0001t0009g0068 others(3): Show |
6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-1871T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775556 | |||||||
chr5:65775870 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-1557A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65775870 | |||||||
chr5:65776005 | C | A | 1 | a0001c0002t0001g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.451-1422C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776005 | |||||||
chr5:65776479 | C | T | 90 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0120 others(87): Show |
98 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.451-948C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776479 | |||||||
chr5:65776798 | C | T | 1 | a0001c0001t0042g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.451-629C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65776798 | |||||||
chr5:65777036 | C | T | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-391C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777036 | |||||||
chr5:65777079 | G | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.451-348G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777079 | |||||||
chr5:65777330 | C | T | 8 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-97C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777330 | |||||||
chr5:65777397 | C | A | 282 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(279): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.451-30C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 3/12 | chr5 | 65777397 | |||||||
chr5:65777562 | G | GA | 8 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0002g0098 others(5): Show |
8 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+38dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 65777562 | ||||||
chr5:65777722 | G | A | 1 | a0001c0002t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.558+188G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777722 | |||||||
chr5:65777890 | G | T | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.558+356G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777890 | |||||||
chr5:65777915 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.558+381A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777915 | |||||||
chr5:65777923 | G | A | 51 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(48): Show |
52 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.558+389G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65777923 | |||||||
chr5:65778310 | A | G | 2 | a0002c0003t0010g0260 a0002c0003t0010g0269 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.558+776A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778310 | |||||||
chr5:65778331 | G | T | 1 | a0002c0004t0007g0244 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.558+797G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778331 | |||||||
chr5:65778334 | C | G | 3 | a0004c0006t0008g0221 a0006c0008t0006g0103 a0006c0008t0006g0177 |
3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.558+800C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778334 | |||||||
chr5:65778656 | G | A | 2 | a0004c0006t0001g0009 a0004c0006t0001g0107 |
3 | NA19030.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.558+1122G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778656 | |||||||
chr5:65778703 | G | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.558+1169G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778703 | |||||||
chr5:65778865 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.559-1314T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778865 | |||||||
chr5:65778890 | G | A | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.559-1289G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778890 | |||||||
chr5:65778891 | T | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.559-1288T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778891 | |||||||
chr5:65778934 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.559-1245G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65778934 | |||||||
chr5:65779009 | G | T | 1 | a0001c0001t0004g0300 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.559-1170G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779009 | |||||||
chr5:65779113 | G | A | 1 | a0001c0001t0005g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.559-1066G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779113 | |||||||
chr5:65779117 | G | A | 51 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(48): Show |
52 | HG00741.hp2 HG01243.hp2 HG01256.hp1 others(49): Show |
intron_variant | MODIFIER | c.559-1062G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779117 | |||||||
chr5:65779210 | C | T | 282 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(279): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.559-969C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779210 | |||||||
chr5:65779427 | C | T | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-752C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779427 | |||||||
chr5:65779487 | C | A | 1 | a0001c0001t0004g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.559-692C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779487 | |||||||
chr5:65779496 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.559-683C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779496 | |||||||
chr5:65779704 | A | G | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.559-475A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779704 | |||||||
chr5:65779835 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.559-344G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779835 | |||||||
chr5:65779869 | T | G | 1 | a0001c0001t0006g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.559-310T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65779869 | |||||||
chr5:65779887 | T | TA | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.559-291dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 65779887 | ||||||
chr5:65780022 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0149 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.559-157C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780022 | |||||||
chr5:65780031 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.559-148A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780031 | |||||||
chr5:65780038 | C | A | 2 | a0001c0001t0048g0264 a0002c0004t0040g0310 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.559-141C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780038 | |||||||
chr5:65780115 | C | A | 13 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0001c0011t0005g0021 others(10): Show |
14 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.559-64C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780115 | |||||||
chr5:65780133 | A | C | 3 | a0004c0006t0008g0221 a0006c0008t0006g0103 a0006c0008t0006g0177 |
3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.559-46A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 4/12 | chr5 | 65780133 | |||||||
chr5:65780311 | C | A | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+30C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780311 | |||||||
chr5:65780329 | A | C | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+48A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780329 | |||||||
chr5:65780444 | A | G | 2 | a0007c0010t0001g0105 a0008c0012t0001g0106 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.661+163A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780444 | |||||||
chr5:65780643 | C | G | 1 | a0002c0004t0016g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+362C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780643 | |||||||
chr5:65780735 | G | A | 1 | a0001c0001t0004g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.661+454G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780735 | |||||||
chr5:65780791 | A | T | 1 | a0001c0001t0005g0234 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.662-470A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780791 | |||||||
chr5:65780831 | G | A | 8 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0002g0098 others(5): Show |
8 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-430G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 5/12 | chr5 | 65780831 | |||||||
chr5:65781705 | G | A | 1 | a0002c0004t0007g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+284G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65781705 | |||||||
chr5:65781909 | G | C | 19 | a0001c0001t0001g0178 a0001c0001t0001g0239 a0001c0001t0001g0240 others(16): Show |
20 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+488G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65781909 | |||||||
chr5:65782018 | C | T | 1 | a0002c0004t0007g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+597C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782018 | |||||||
chr5:65782045 | G | T | 1 | a0001c0001t0002g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.822+624G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782045 | |||||||
chr5:65782083 | T | G | 51 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(48): Show |
52 | HG00741.hp2 HG01074.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.822+662T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782083 | |||||||
chr5:65782198 | T | A | 133 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(130): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.822+777T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782198 | |||||||
chr5:65782358 | T | C | 7 | a0001c0001t0002g0246 a0001c0001t0015g0043 a0001c0001t0015g0249 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+937T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782358 | |||||||
chr5:65782417 | A | G | 1 | a0002c0004t0007g0244 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.822+996A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782417 | |||||||
chr5:65782504 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.822+1083T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782504 | |||||||
chr5:65782808 | A | G | 1 | a0002c0004t0007g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.822+1387A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65782808 | |||||||
chr5:65783008 | C | G | 2 | a0001c0001t0003g0071 a0001c0001t0003g0074 |
2 | NA18974.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.822+1587C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783008 | |||||||
chr5:65783219 | T | C | 2 | a0001c0001t0004g0280 a0001c0001t0004g0297 |
2 | HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.822+1798T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783219 | |||||||
chr5:65783292 | C | T | 26 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0001c0001t0006g0028 others(23): Show |
27 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.822+1871C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783292 | |||||||
chr5:65783506 | G | T | 1 | a0001c0001t0025g0020 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.822+2085G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783506 | |||||||
chr5:65783533 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0028g0179 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.822+2112G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783533 | |||||||
chr5:65783538 | G | A | 2 | a0001c0001t0005g0052 a0001c0001t0005g0169 |
2 | NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.822+2117G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783538 | |||||||
chr5:65783584 | G | A | 52 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(49): Show |
53 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(50): Show |
intron_variant | MODIFIER | c.822+2163G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783584 | |||||||
chr5:65783651 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-2124G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783651 | |||||||
chr5:65783703 | T | TA | 143 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0127 others(140): Show |
154 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.823-2056dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65783703 | ||||||
chr5:65783784 | G | T | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.823-1991G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65783784 | |||||||
chr5:65784017 | T | G | 202 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0057 others(199): Show |
216 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(213): Show |
intron_variant | MODIFIER | c.823-1758T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784017 | |||||||
chr5:65784264 | C | T | 256 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0050 others(253): Show |
271 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(268): Show |
intron_variant | MODIFIER | c.823-1511C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784264 | |||||||
chr5:65784273 | TAATAA | T | 145 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0120 others(142): Show |
156 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.823-1496_823-1492d others(7): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65784273 | ||||||
chr5:65784322 | A | C | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
10 | HG01243.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-1453A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784322 | |||||||
chr5:65784369 | A | G | 1 | a0002c0003t0010g0286 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-1406A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784369 | |||||||
chr5:65784594 | A | G | 1 | a0001c0002t0012g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.823-1181A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784594 | |||||||
chr5:65784657 | G | T | 3 | a0004c0006t0008g0221 a0006c0008t0006g0103 a0006c0008t0006g0177 |
3 | HG02976.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.823-1118G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784657 | |||||||
chr5:65784707 | G | T | 21 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0001c0011t0005g0021 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.823-1068G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784707 | |||||||
chr5:65784753 | G | A | 91 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0120 others(88): Show |
99 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.823-1022G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784753 | |||||||
chr5:65784982 | T | C | 1 | a0001c0001t0036g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.823-793T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65784982 | |||||||
chr5:65785038 | T | C | 8 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0002g0098 others(5): Show |
8 | HG01256.hp1 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-737T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785038 | |||||||
chr5:65785169 | A | G | 121 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0120 others(118): Show |
131 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.823-606A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785169 | |||||||
chr5:65785219 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.823-556A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785219 | |||||||
chr5:65785242 | C | T | 5 | a0001c0001t0002g0257 a0001c0001t0004g0281 a0002c0004t0043g0258 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-533C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785242 | |||||||
chr5:65785339 | A | T | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.823-436A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785339 | |||||||
chr5:65785389 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823-386G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785389 | |||||||
chr5:65785605 | CA | C | 32 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(29): Show |
32 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.823-154delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65785605 | ||||||
chr5:65785605 | CAA | C | 25 | a0001c0001t0005g0261 a0001c0001t0006g0028 a0001c0001t0006g0262 others(22): Show |
28 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.823-155_823-154del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 65785605 | ||||||
chr5:65785623 | C | T | 1 | a0001c0002t0012g0176 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.823-152C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 6/12 | chr5 | 65785623 | |||||||
chr5:65786046 | G | A | 1 | a0001c0001t0004g0301 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.958+136G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786046 | |||||||
chr5:65786050 | T | A | 55 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(52): Show |
56 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.958+140T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786050 | |||||||
chr5:65786278 | C | T | 52 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(49): Show |
53 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(50): Show |
intron_variant | MODIFIER | c.958+368C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786278 | |||||||
chr5:65786617 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.958+707G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786617 | |||||||
chr5:65786753 | T | C | 3 | a0001c0007t0018g0289 a0001c0007t0018g0291 a0001c0007t0018g0303 |
3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.958+843T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786753 | |||||||
chr5:65786974 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.958+1064G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65786974 | |||||||
chr5:65787023 | T | G | 21 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0001c0011t0005g0021 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.959-1095T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787023 | |||||||
chr5:65787030 | G | A | 2 | a0001c0001t0004g0302 a0001c0001t0055g0304 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.959-1088G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787030 | |||||||
chr5:65787115 | T | C | 26 | a0001c0001t0001g0050 a0001c0001t0001g0216 a0001c0001t0001g0226 others(23): Show |
26 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.959-1003T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787115 | |||||||
chr5:65787156 | G | A | 4 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 others(1): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.959-962G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787156 | |||||||
chr5:65787173 | A | T | 49 | a0001c0001t0001g0037 a0001c0001t0001g0114 a0001c0001t0001g0149 others(46): Show |
50 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.959-945A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787173 | |||||||
chr5:65787252 | G | A | 3 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 |
4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-866G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787252 | |||||||
chr5:65787254 | A | ATG | 63 | a0001c0001t0001g0050 a0001c0001t0001g0178 a0001c0001t0001g0216 others(60): Show |
67 | HG00741.hp2 HG01243.hp2 HG01516.hp2 others(64): Show |
intron_variant | MODIFIER | c.959-844_959-843dup others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787254 | ||||||
chr5:65787254 | A | G | 3 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 |
4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-864A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787254 | |||||||
chr5:65787254 | ATG | A | 2 | a0001c0002t0001g0119 a0003c0005t0020g0018 |
3 | HG02896.hp2 HG02897.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.959-844_959-843del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787254 | ||||||
chr5:65787256 | G | A | 3 | a0001c0001t0005g0261 a0001c0001t0006g0262 a0001c0001t0019g0019 |
4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.959-862G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787256 | |||||||
chr5:65787288 | GCA | G | 3 | a0001c0001t0015g0043 a0001c0001t0015g0249 a0001c0001t0015g0250 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.959-823_959-822del others(2): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 65787288 | ||||||
chr5:65787308 | G | A | 20 | a0001c0001t0006g0028 a0001c0011t0005g0021 a0002c0003t0007g0085 others(17): Show |
21 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.959-810G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787308 | |||||||
chr5:65787321 | T | C | 110 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0114 others(107): Show |
115 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.959-797T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787321 | |||||||
chr5:65787332 | A | G | 1 | a0001c0002t0001g0030 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.959-786A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787332 | |||||||
chr5:65787382 | C | T | 7 | a0001c0001t0001g0180 a0001c0001t0009g0024 a0001c0001t0009g0027 others(4): Show |
7 | HG00323.hp2 HG01070.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.959-736C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787382 | |||||||
chr5:65787435 | A | G | 1 | a0001c0013t0038g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.959-683A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787435 | |||||||
chr5:65787515 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.959-603A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787515 | |||||||
chr5:65787869 | G | C | 9 | a0001c0001t0006g0102 a0001c0001t0006g0104 a0001c0001t0006g0110 others(6): Show |
12 | HG01884.hp1 HG02258.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.959-249G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787869 | |||||||
chr5:65787907 | A | G | 1 | a0001c0001t0004g0271 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.959-211A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787907 | |||||||
chr5:65787969 | G | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0139 others(70): Show |
81 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.959-149G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787969 | |||||||
chr5:65787981 | C | T | 1 | a0001c0001t0028g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959-137C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65787981 | |||||||
chr5:65788038 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0141 others(47): Show |
58 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.959-80A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 7/12 | chr5 | 65788038 | |||||||
chr5:65788738 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0160 |
2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1325+254G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788738 | |||||||
chr5:65788769 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1325+285C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788769 | |||||||
chr5:65788859 | G | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0139 others(2): Show |
5 | HG00642.hp2 HG01123.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325+375G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65788859 | |||||||
chr5:65788971 | C | CA | 92 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(89): Show |
95 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1325+500dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 65788971 | ||||||
chr5:65788971 | CA | C | 10 | a0001c0001t0008g0002 a0001c0001t0008g0008 a0001c0001t0008g0219 others(7): Show |
13 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+500delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 65788971 | ||||||
chr5:65789067 | A | G | 2 | a0001c0001t0031g0254 a0005c0009t0035g0255 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1325+583A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789067 | |||||||
chr5:65789116 | G | A | 10 | a0001c0001t0008g0002 a0001c0001t0008g0008 a0001c0001t0008g0219 others(7): Show |
13 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+632G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789116 | |||||||
chr5:65789323 | A | G | 1 | a0004c0006t0008g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1325+839A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789323 | |||||||
chr5:65789371 | T | C | 3 | a0002c0004t0007g0244 a0002c0004t0007g0245 a0002c0004t0007g0248 |
3 | HG02965.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1325+887T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789371 | |||||||
chr5:65789493 | C | A | 1 | a0001c0002t0001g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1325+1009C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789493 | |||||||
chr5:65789503 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(95): Show |
103 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1325+1019A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789503 | |||||||
chr5:65789755 | A | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0161 a0001c0001t0004g0295 others(3): Show |
6 | NA18983.hp1 NA18993.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+1271A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789755 | |||||||
chr5:65789756 | T | C | 1 | a0001c0001t0021g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1325+1272T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789756 | |||||||
chr5:65789797 | C | T | 35 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0046 others(32): Show |
38 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325+1313C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789797 | |||||||
chr5:65789845 | A | G | 35 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0046 others(32): Show |
38 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325+1361A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65789845 | |||||||
chr5:65790081 | A | T | 1 | a0002c0004t0016g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1325+1597A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790081 | |||||||
chr5:65790130 | C | A | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1325+1646C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790130 | |||||||
chr5:65790204 | T | G | 25 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0046 others(22): Show |
25 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.1325+1720T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790204 | |||||||
chr5:65790469 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(164): Show |
175 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1325+1985A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790469 | |||||||
chr5:65790541 | A | C | 6 | a0001c0001t0002g0181 a0001c0001t0002g0186 a0001c0001t0002g0187 others(3): Show |
6 | HG00621.hp2 NA18747.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-1913A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790541 | |||||||
chr5:65790571 | A | G | 4 | a0001c0001t0011g0222 a0001c0001t0011g0227 a0001c0001t0011g0235 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-1883A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790571 | |||||||
chr5:65790624 | C | T | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1830C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790624 | |||||||
chr5:65790641 | G | A | 11 | a0001c0001t0031g0254 a0001c0001t0039g0151 a0001c0001t0052g0283 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-1813G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790641 | |||||||
chr5:65790800 | T | G | 45 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(42): Show |
51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1326-1654T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790800 | |||||||
chr5:65790806 | G | A | 1 | a0001c0001t0004g0297 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1326-1648G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790806 | |||||||
chr5:65790877 | G | A | 1 | a0001c0002t0013g0162 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1326-1577G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790877 | |||||||
chr5:65790949 | G | A | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-1505G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65790949 | |||||||
chr5:65791023 | A | C | 34 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(31): Show |
36 | HG00609.hp1 HG01070.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1326-1431A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791023 | |||||||
chr5:65791106 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1326-1348A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791106 | |||||||
chr5:65791258 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(164): Show |
175 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1326-1196G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791258 | |||||||
chr5:65791284 | A | C | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1170A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791284 | |||||||
chr5:65791378 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(164): Show |
175 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1326-1076G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791378 | |||||||
chr5:65791409 | T | G | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1326-1045T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791409 | |||||||
chr5:65791493 | C | T | 1 | a0001c0001t0005g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1326-961C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791493 | |||||||
chr5:65791494 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(164): Show |
175 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1326-960A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791494 | |||||||
chr5:65791530 | C | A | 68 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0001t0001g0133 others(65): Show |
71 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1326-924C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791530 | |||||||
chr5:65791543 | G | A | 7 | a0001c0001t0039g0151 a0001c0001t0052g0283 a0001c0001t0053g0299 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-911G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791543 | |||||||
chr5:65791553 | G | A | 7 | a0001c0001t0039g0151 a0001c0001t0052g0283 a0001c0001t0053g0299 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326-901G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791553 | |||||||
chr5:65791593 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(164): Show |
175 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1326-861T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791593 | |||||||
chr5:65791602 | A | G | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-852A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791602 | |||||||
chr5:65791704 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(84): Show |
92 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1326-750C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791704 | |||||||
chr5:65791729 | A | T | 1 | a0001c0001t0005g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1326-725A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791729 | |||||||
chr5:65791730 | A | T | 11 | a0001c0001t0031g0254 a0001c0001t0039g0151 a0001c0001t0052g0283 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-724A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65791730 | |||||||
chr5:65792348 | G | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(96): Show |
105 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.1326-106G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65792348 | |||||||
chr5:65792434 | C | T | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1326-20C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 8/12 | chr5 | 65792434 | |||||||
chr5:65792660 | GT | G | 7 | a0001c0001t0001g0195 a0001c0001t0031g0254 a0003c0005t0022g0083 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1527+15delT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65792660 | ||||||
chr5:65792751 | GA | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0185 others(2): Show |
6 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1527+98delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65792751 | ||||||
chr5:65792905 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1527+250T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65792905 | |||||||
chr5:65792941 | T | G | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1527+286T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65792941 | |||||||
chr5:65793340 | G | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(122): Show |
129 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1527+685G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793340 | |||||||
chr5:65793505 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1527+850G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793505 | |||||||
chr5:65793630 | TA | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(117): Show |
124 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1527+989delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65793630 | ||||||
chr5:65793698 | T | C | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1527+1043T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793698 | |||||||
chr5:65793952 | T | G | 64 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0001t0001g0133 others(61): Show |
65 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1527+1297T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793952 | |||||||
chr5:65793995 | G | A | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1340G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65793995 | |||||||
chr5:65794098 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1527+1443G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794098 | |||||||
chr5:65794154 | G | T | 3 | a0001c0001t0002g0257 a0002c0004t0040g0310 a0002c0004t0043g0258 |
3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1499G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794154 | |||||||
chr5:65794183 | C | T | 3 | a0001c0001t0002g0257 a0002c0004t0040g0310 a0002c0004t0043g0258 |
3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+1528C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794183 | |||||||
chr5:65794263 | A | G | 1 | a0002c0003t0010g0269 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1527+1608A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794263 | |||||||
chr5:65794400 | C | G | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+1745C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794400 | |||||||
chr5:65794427 | A | G | 1 | a0001c0001t0056g0259 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1527+1772A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794427 | |||||||
chr5:65794561 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1527+1906C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794561 | |||||||
chr5:65794656 | C | T | 1 | a0008c0012t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1527+2001C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794656 | |||||||
chr5:65794717 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0156 a0001c0001t0009g0058 others(1): Show |
4 | HG01496.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+2062C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794717 | |||||||
chr5:65794718 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(121): Show |
128 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1527+2063G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794718 | |||||||
chr5:65794727 | A | G | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+2072A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794727 | |||||||
chr5:65794804 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1527+2149C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794804 | |||||||
chr5:65794983 | TTTTAATC others(32): Show |
T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0052 a0001c0001t0005g0169 |
3 | NA18992.hp1 NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1527+2329_1527+236 others(43): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65794983 | |||||||
chr5:65795082 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1527+2427G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795082 | |||||||
chr5:65795118 | C | T | 1 | a0001c0001t0004g0300 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1527+2463C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795118 | |||||||
chr5:65795217 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(223): Show |
240 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.1527+2562C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795217 | |||||||
chr5:65795241 | G | A | 52 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(49): Show |
60 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1527+2586G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795241 | |||||||
chr5:65795247 | G | A | 1 | a0001c0001t0014g0130 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1527+2592G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795247 | |||||||
chr5:65795351 | G | T | 3 | a0002c0003t0007g0137 a0002c0003t0007g0228 a0002c0003t0007g0229 |
3 | HG00738.hp1 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1527+2696G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795351 | |||||||
chr5:65795638 | G | A | 4 | a0003c0005t0022g0083 a0003c0005t0022g0084 a0003c0005t0023g0060 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1527+2983G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795638 | |||||||
chr5:65795746 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1527+3091G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795746 | |||||||
chr5:65795825 | T | A | 1 | a0002c0004t0007g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1527+3170T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65795825 | |||||||
chr5:65796060 | C | T | 4 | a0003c0005t0022g0083 a0003c0005t0022g0084 a0003c0005t0023g0060 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1527+3405C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796060 | |||||||
chr5:65796118 | C | T | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+3463C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796118 | |||||||
chr5:65796153 | C | A | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1527+3498C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796153 | |||||||
chr5:65796270 | T | G | 1 | a0001c0001t0003g0076 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1527+3615T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796270 | |||||||
chr5:65796320 | T | G | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1527+3665T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796320 | |||||||
chr5:65796896 | T | A | 27 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0046 others(24): Show |
28 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.1527+4241T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65796896 | |||||||
chr5:65797052 | C | T | 3 | a0002c0004t0007g0244 a0002c0004t0007g0245 a0002c0004t0007g0248 |
3 | HG02965.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1527+4397C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797052 | |||||||
chr5:65797143 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1527+4488T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797143 | |||||||
chr5:65797313 | C | A | 1 | a0001c0002t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1527+4658C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797313 | |||||||
chr5:65797812 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1527+5157C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797812 | |||||||
chr5:65797826 | C | G | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+5171C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797826 | |||||||
chr5:65797883 | T | C | 2 | a0001c0001t0015g0249 a0001c0001t0015g0250 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1527+5228T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797883 | |||||||
chr5:65797896 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1527+5241C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797896 | |||||||
chr5:65797937 | A | G | 1 | a0001c0001t0004g0300 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1527+5282A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65797937 | |||||||
chr5:65798000 | G | A | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+5345G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798000 | |||||||
chr5:65798018 | T | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(50): Show |
56 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1527+5363T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798018 | |||||||
chr5:65798052 | GAAGCGAA others(4): Show |
G | 1 | a0001c0001t0052g0283 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1527+5412_1527+542 others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65798052 | ||||||
chr5:65798181 | C | T | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1527+5526C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798181 | |||||||
chr5:65798417 | C | T | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1527+5762C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798417 | |||||||
chr5:65798478 | A | G | 1 | a0002c0003t0041g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1527+5823A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798478 | |||||||
chr5:65798577 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1527+5922C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798577 | |||||||
chr5:65798642 | A | G | 21 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0046 others(18): Show |
21 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1527+5987A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798642 | |||||||
chr5:65798907 | G | T | 52 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(49): Show |
60 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1527+6252G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798907 | |||||||
chr5:65798982 | G | A | 1 | a0003c0005t0021g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1527+6327G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65798982 | |||||||
chr5:65799035 | C | T | 5 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1527+6380C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799035 | |||||||
chr5:65799050 | T | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(84): Show |
90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1527+6395T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799050 | |||||||
chr5:65799080 | C | G | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+6425C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799080 | |||||||
chr5:65799276 | A | G | 1 | a0001c0002t0004g0287 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1527+6621A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799276 | |||||||
chr5:65799295 | A | G | 55 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(52): Show |
63 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1527+6640A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799295 | |||||||
chr5:65799424 | C | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0205 others(1): Show |
5 | NA18962.hp2 NA18964.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1527+6769C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799424 | |||||||
chr5:65799427 | G | C | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+6772G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799427 | |||||||
chr5:65799573 | C | A | 1 | a0001c0001t0042g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1527+6918C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799573 | |||||||
chr5:65799637 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1527+6982G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799637 | |||||||
chr5:65799654 | A | T | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1527+6999A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799654 | |||||||
chr5:65799714 | A | G | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1527+7059A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799714 | |||||||
chr5:65799724 | A | G | 2 | a0001c0002t0001g0126 a0001c0002t0001g0200 |
2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1527+7069A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65799724 | |||||||
chr5:65799917 | T | TA | 57 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(54): Show |
65 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1527+7272dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65799917 | ||||||
chr5:65800156 | T | C | 10 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1527+7501T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800156 | |||||||
chr5:65800234 | T | G | 1 | a0001c0001t0028g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1527+7579T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800234 | |||||||
chr5:65800339 | C | T | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1527+7684C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800339 | |||||||
chr5:65800472 | G | A | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1527+7817G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800472 | |||||||
chr5:65800489 | C | T | 1 | a0001c0001t0014g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1527+7834C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800489 | |||||||
chr5:65800663 | C | CTTAT | 146 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(143): Show |
158 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.1527+8043_1527+804 others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTATTTA others(1): Show |
27 | a0001c0001t0001g0226 a0001c0001t0002g0098 a0001c0001t0002g0099 others(24): Show |
28 | HG00738.hp1 HG00741.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1527+8039_1527+804 others(12): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTATTTA others(5): Show |
8 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1527+8035_1527+804 others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTATTTA others(9): Show |
2 | a0001c0001t0002g0257 a0003c0005t0023g0060 |
2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1527+8031_1527+804 others(20): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTTTTAT others(4): Show |
1 | a0001c0001t0005g0232 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1527+8010_1527+801 others(15): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTTTTAT others(8): Show |
53 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0001t0001g0133 others(50): Show |
54 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1527+8010_1527+801 others(19): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800663 | C | CTTTTTAT others(12): Show |
7 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0004g0280 others(4): Show |
7 | HG01261.hp1 HG02132.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1527+8010_1527+801 others(23): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65800663 | ||||||
chr5:65800840 | A | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1527+8185A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65800840 | |||||||
chr5:65801237 | T | G | 1 | a0001c0001t0006g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1528-8278T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801237 | |||||||
chr5:65801404 | G | T | 2 | a0001c0001t0006g0102 a0001c0001t0006g0110 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1528-8111G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801404 | |||||||
chr5:65801427 | T | C | 1 | a0001c0002t0001g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1528-8088T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801427 | |||||||
chr5:65801474 | G | T | 30 | a0001c0001t0002g0257 a0001c0001t0005g0035 a0001c0001t0005g0036 others(27): Show |
31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-8041G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801474 | |||||||
chr5:65801509 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1528-8006A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801509 | |||||||
chr5:65801631 | C | G | 2 | a0001c0002t0001g0136 a0001c0002t0004g0287 |
2 | HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1528-7884C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801631 | |||||||
chr5:65801806 | A | AT | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-7708dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65801806 | ||||||
chr5:65801818 | T | TG | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-7697_1528-769 others(5): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801818 | |||||||
chr5:65801923 | G | A | 1 | a0001c0002t0001g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1528-7592G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801923 | |||||||
chr5:65801977 | A | T | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1528-7538A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65801977 | |||||||
chr5:65802043 | C | T | 1 | a0001c0001t0009g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1528-7472C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802043 | |||||||
chr5:65802185 | C | G | 1 | a0001c0001t0004g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1528-7330C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802185 | |||||||
chr5:65802300 | G | A | 1 | a0002c0003t0017g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1528-7215G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802300 | |||||||
chr5:65802301 | G | T | 62 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(59): Show |
70 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1528-7214G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802301 | |||||||
chr5:65802363 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1528-7152C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802363 | |||||||
chr5:65802404 | G | T | 30 | a0001c0001t0002g0257 a0001c0001t0005g0035 a0001c0001t0005g0036 others(27): Show |
31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-7111G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802404 | |||||||
chr5:65802427 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1528-7088C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802427 | |||||||
chr5:65802435 | C | T | 1 | a0001c0013t0038g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1528-7080C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802435 | |||||||
chr5:65802436 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1528-7079G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802436 | |||||||
chr5:65802668 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1528-6847G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802668 | |||||||
chr5:65802718 | C | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(153): Show |
162 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1528-6797C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802718 | |||||||
chr5:65802885 | G | A | 54 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(51): Show |
62 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1528-6630G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65802885 | |||||||
chr5:65803098 | G | A | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-6417G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803098 | |||||||
chr5:65803211 | T | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-6304T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803211 | |||||||
chr5:65803251 | C | T | 62 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(59): Show |
70 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1528-6264C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803251 | |||||||
chr5:65803255 | C | T | 1 | a0002c0004t0017g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1528-6260C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803255 | |||||||
chr5:65803336 | C | T | 61 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0001t0001g0133 others(58): Show |
62 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1528-6179C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803336 | |||||||
chr5:65803401 | G | T | 1 | a0001c0001t0002g0143 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1528-6114G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803401 | |||||||
chr5:65803408 | A | C | 2 | a0003c0005t0020g0018 a0003c0005t0021g0086 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1528-6107A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803408 | |||||||
chr5:65803417 | C | T | 55 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(52): Show |
63 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1528-6098C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803417 | |||||||
chr5:65803510 | G | C | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1528-6005G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803510 | |||||||
chr5:65803602 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1528-5913C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803602 | |||||||
chr5:65803799 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(89): Show |
97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1528-5716C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803799 | |||||||
chr5:65803807 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1528-5708G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803807 | |||||||
chr5:65803850 | T | C | 3 | a0004c0006t0001g0009 a0004c0006t0001g0101 a0004c0006t0001g0107 |
4 | HG02451.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1528-5665T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803850 | |||||||
chr5:65803889 | C | T | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-5626C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65803889 | |||||||
chr5:65804331 | G | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-5184G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804331 | |||||||
chr5:65804390 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1528-5125T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804390 | |||||||
chr5:65804397 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1528-5118T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804397 | |||||||
chr5:65804571 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-4944T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804571 | |||||||
chr5:65804690 | A | C | 1 | a0001c0014t0057g0306 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1528-4825A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804690 | |||||||
chr5:65804741 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(220): Show |
237 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1528-4774A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804741 | |||||||
chr5:65804833 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-4682T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804833 | |||||||
chr5:65804942 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1528-4573A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804942 | |||||||
chr5:65804954 | G | A | 3 | a0001c0001t0006g0028 a0001c0001t0031g0254 a0005c0009t0035g0255 |
3 | HG01243.hp1 HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1528-4561G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65804954 | |||||||
chr5:65805135 | A | G | 61 | a0001c0001t0001g0050 a0001c0001t0001g0120 a0001c0001t0001g0133 others(58): Show |
62 | HG00323.hp2 HG00438.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1528-4380A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805135 | |||||||
chr5:65805632 | T | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1528-3883T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805632 | |||||||
chr5:65805749 | C | T | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-3766C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805749 | |||||||
chr5:65805809 | G | A | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-3706G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805809 | |||||||
chr5:65805843 | A | G | 4 | a0001c0001t0015g0043 a0001c0001t0015g0249 a0001c0001t0015g0250 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-3672A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805843 | |||||||
chr5:65805886 | T | G | 1 | a0002c0003t0041g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1528-3629T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65805886 | |||||||
chr5:65806233 | T | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-3282T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806233 | |||||||
chr5:65806294 | A | G | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-3221A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806294 | |||||||
chr5:65806413 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1528-3102T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806413 | |||||||
chr5:65806426 | G | C | 2 | a0001c0001t0006g0102 a0001c0001t0006g0110 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1528-3089G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806426 | |||||||
chr5:65806450 | T | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-3065T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806450 | |||||||
chr5:65806639 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1528-2876A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806639 | |||||||
chr5:65806674 | C | T | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-2841C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806674 | |||||||
chr5:65806735 | T | G | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-2780T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65806735 | |||||||
chr5:65807012 | A | G | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1528-2503A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807012 | |||||||
chr5:65807071 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1528-2444G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807071 | |||||||
chr5:65807173 | T | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-2342T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807173 | |||||||
chr5:65807176 | CA | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(214): Show |
231 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1528-2326delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65807176 | ||||||
chr5:65807338 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(89): Show |
97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1528-2177C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807338 | |||||||
chr5:65807438 | A | AT | 6 | a0001c0001t0002g0207 a0001c0002t0001g0158 a0002c0004t0017g0277 others(3): Show |
6 | HG01167.hp2 HG03471.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1528-2065dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 65807438 | ||||||
chr5:65807561 | C | T | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1528-1954C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807561 | |||||||
chr5:65807589 | C | T | 1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1528-1926C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807589 | |||||||
chr5:65807597 | T | G | 6 | a0001c0001t0008g0002 a0001c0001t0008g0008 a0001c0001t0008g0219 others(3): Show |
9 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1528-1918T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65807597 | |||||||
chr5:65808088 | G | A | 4 | a0001c0002t0001g0010 a0001c0002t0001g0118 a0001c0002t0001g0140 others(1): Show |
5 | HG01255.hp2 HG01358.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1528-1427G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808088 | |||||||
chr5:65808098 | G | A | 30 | a0001c0001t0002g0257 a0001c0001t0005g0035 a0001c0001t0005g0036 others(27): Show |
31 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1528-1417G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808098 | |||||||
chr5:65808319 | G | A | 2 | a0001c0002t0001g0211 a0001c0002t0001g0213 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1528-1196G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808319 | |||||||
chr5:65808516 | A | G | 1 | a0002c0004t0007g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1528-999A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808516 | |||||||
chr5:65808845 | A | T | 4 | a0001c0001t0015g0043 a0001c0001t0015g0249 a0001c0001t0015g0250 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-670A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808845 | |||||||
chr5:65808909 | C | T | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-606C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808909 | |||||||
chr5:65808942 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1528-573A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808942 | |||||||
chr5:65808972 | C | G | 1 | a0001c0002t0001g0125 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1528-543C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65808972 | |||||||
chr5:65809130 | C | T | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1528-385C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809130 | |||||||
chr5:65809369 | C | T | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1528-146C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809369 | |||||||
chr5:65809381 | G | A | 3 | a0001c0002t0001g0010 a0001c0002t0001g0118 a0001c0002t0001g0140 |
4 | HG01255.hp2 HG01358.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528-134G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 9/12 | chr5 | 65809381 | |||||||
chr5:65809795 | G | A | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1714+94G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 10/12 | chr5 | 65809795 | |||||||
chr5:65810354 | G | C | 5 | a0001c0001t0002g0181 a0001c0001t0002g0186 a0001c0001t0002g0187 others(2): Show |
5 | NA18747.hp2 NA18942.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1843+189G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810354 | |||||||
chr5:65810400 | T | C | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1843+235T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810400 | |||||||
chr5:65810433 | G | A | 2 | a0001c0001t0004g0265 a0001c0001t0004g0279 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1843+268G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810433 | |||||||
chr5:65810607 | C | T | 10 | a0001c0001t0006g0023 a0001c0001t0006g0044 a0001c0001t0006g0047 others(7): Show |
10 | HG00741.hp2 HG01167.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1843+442C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810607 | |||||||
chr5:65810965 | T | C | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1843+800T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810965 | |||||||
chr5:65810973 | T | C | 1 | a0001c0001t0003g0079 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1843+808T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65810973 | |||||||
chr5:65811111 | T | G | 1 | a0001c0001t0002g0238 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1843+946T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811111 | |||||||
chr5:65811112 | T | A | 1 | a0001c0001t0002g0238 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1843+947T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811112 | |||||||
chr5:65811152 | A | T | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843+987A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811152 | |||||||
chr5:65811170 | G | A | 5 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843+1005G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811170 | |||||||
chr5:65811425 | C | G | 46 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(43): Show |
51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1844-830C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811425 | |||||||
chr5:65811447 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1844-808G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811447 | |||||||
chr5:65811515 | T | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(92): Show |
100 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1844-740T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811515 | |||||||
chr5:65811546 | G | A | 6 | a0001c0001t0008g0002 a0001c0001t0008g0008 a0001c0001t0008g0219 others(3): Show |
9 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1844-709G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811546 | |||||||
chr5:65811570 | C | G | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1844-685C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811570 | |||||||
chr5:65811628 | C | A | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1844-627C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811628 | |||||||
chr5:65811668 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1844-587T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811668 | |||||||
chr5:65811762 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(89): Show |
97 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1844-493C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811762 | |||||||
chr5:65811851 | A | T | 2 | a0002c0004t0016g0088 a0002c0016t0034g0256 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1844-404A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811851 | |||||||
chr5:65811989 | C | T | 1 | a0001c0002t0001g0025 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1844-266C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65811989 | |||||||
chr5:65812215 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1844-40G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812215 | |||||||
chr5:65812222 | A | G | 1 | a0001c0001t0004g0293 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1844-33A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812222 | |||||||
chr5:65812242 | T | C | 1 | a0002c0003t0041g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1844-13T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 11/12 | chr5 | 65812242 | |||||||
chr5:65812428 | G | A | 3 | a0001c0007t0018g0289 a0001c0007t0018g0291 a0001c0007t0018g0303 |
3 | HG00438.hp1 NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1980+37G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812428 | |||||||
chr5:65812485 | G | T | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+94G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812485 | |||||||
chr5:65812582 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(220): Show |
237 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1980+191T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812582 | |||||||
chr5:65812739 | G | T | 3 | a0001c0001t0002g0257 a0002c0004t0040g0310 a0002c0004t0043g0258 |
3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+348G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812739 | |||||||
chr5:65812947 | C | A | 1 | a0001c0002t0001g0092 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1980+556C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65812947 | |||||||
chr5:65813049 | C | T | 218 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(215): Show |
232 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.1980+658C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813049 | |||||||
chr5:65813179 | A | C | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1980+788A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813179 | |||||||
chr5:65813365 | C | G | 5 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980+974C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813365 | |||||||
chr5:65813423 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1980+1032C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813423 | |||||||
chr5:65813782 | G | A | 3 | a0001c0001t0002g0257 a0002c0004t0040g0310 a0002c0004t0043g0258 |
3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+1391G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813782 | |||||||
chr5:65813829 | G | C | 1 | a0001c0002t0001g0100 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1980+1438G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813829 | |||||||
chr5:65813927 | C | CA | 8 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0021g0097 others(5): Show |
9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1980+1549dupA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65813927 | ||||||
chr5:65813941 | T | A | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1980+1550T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813941 | |||||||
chr5:65813992 | C | A | 8 | a0002c0003t0010g0260 a0002c0003t0010g0267 a0002c0003t0010g0269 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+1601C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65813992 | |||||||
chr5:65814013 | G | A | 36 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(33): Show |
38 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1980+1622G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814013 | |||||||
chr5:65814014 | G | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0052 a0001c0001t0005g0169 |
3 | NA18992.hp1 NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1980+1623G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814014 | |||||||
chr5:65814116 | T | C | 1 | a0001c0001t0042g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1980+1725T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814116 | |||||||
chr5:65814416 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0032g0220 a0001c0001t0033g0218 others(1): Show |
4 | HG02451.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+2025G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814416 | |||||||
chr5:65814544 | A | C | 1 | a0001c0001t0005g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1980+2153A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814544 | |||||||
chr5:65814725 | A | G | 212 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(209): Show |
226 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1980+2334A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814725 | |||||||
chr5:65814930 | T | G | 6 | a0001c0001t0002g0257 a0001c0001t0006g0028 a0001c0001t0031g0254 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+2539T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814930 | |||||||
chr5:65814961 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(123): Show |
131 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1980+2570A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65814961 | |||||||
chr5:65815030 | C | T | 1 | a0001c0001t0004g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1980+2639C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815030 | |||||||
chr5:65815072 | A | T | 1 | a0001c0002t0001g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1980+2681A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815072 | |||||||
chr5:65815411 | A | T | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1980+3020A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65815411 | |||||||
chr5:65816011 | C | G | 1 | a0001c0002t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1980+3620C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816011 | |||||||
chr5:65816018 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980+3627T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816018 | |||||||
chr5:65816051 | C | T | 35 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(32): Show |
37 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1980+3660C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816051 | |||||||
chr5:65816064 | A | G | 1 | a0001c0001t0031g0254 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1980+3673A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816064 | |||||||
chr5:65816126 | G | C | 162 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0120 others(159): Show |
173 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(170): Show |
intron_variant | MODIFIER | c.1980+3735G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816126 | |||||||
chr5:65816287 | C | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(49): Show |
55 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1980+3896C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816287 | |||||||
chr5:65816345 | C | T | 2 | a0001c0001t0004g0302 a0001c0001t0055g0304 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1980+3954C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816345 | |||||||
chr5:65816356 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(85): Show |
91 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1980+3965A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816356 | |||||||
chr5:65816523 | G | A | 1 | a0002c0004t0040g0310 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1980+4132G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816523 | |||||||
chr5:65816610 | C | T | 1 | a0004c0006t0029g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1980+4219C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816610 | |||||||
chr5:65816694 | G | A | 2 | a0001c0001t0032g0220 a0001c0001t0051g0298 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1980+4303G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816694 | |||||||
chr5:65816830 | C | G | 1 | a0001c0011t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1980+4439C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816830 | |||||||
chr5:65816901 | T | G | 212 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(209): Show |
226 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1980+4510T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65816901 | |||||||
chr5:65817007 | G | A | 1 | a0001c0002t0001g0197 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1980+4616G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817007 | |||||||
chr5:65817025 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1980+4634A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817025 | |||||||
chr5:65817326 | C | T | 2 | a0003c0005t0022g0083 a0003c0005t0022g0084 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1980+4935C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817326 | |||||||
chr5:65817637 | C | G | 4 | a0001c0001t0015g0043 a0001c0001t0015g0249 a0001c0001t0015g0250 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-5144C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817637 | |||||||
chr5:65817715 | A | G | 5 | a0001c0001t0005g0051 a0001c0001t0005g0164 a0001c0001t0005g0217 others(2): Show |
5 | NA18954.hp2 NA18964.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-5066A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817715 | |||||||
chr5:65817868 | C | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0209 |
2 | NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1981-4913C>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65817868 | |||||||
chr5:65818256 | C | A | 2 | a0001c0001t0002g0257 a0002c0004t0043g0258 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-4525C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818256 | |||||||
chr5:65818331 | T | C | 6 | a0001c0001t0004g0300 a0002c0003t0007g0085 a0002c0003t0007g0137 others(3): Show |
6 | HG00735.hp1 HG00738.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1981-4450T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818331 | |||||||
chr5:65818372 | C | T | 1 | a0001c0001t0056g0259 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1981-4409C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818372 | |||||||
chr5:65818389 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1981-4392C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818389 | |||||||
chr5:65818766 | G | C | 44 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(41): Show |
46 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1981-4015G>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818766 | |||||||
chr5:65818769 | G | A | 1 | a0001c0001t0004g0295 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1981-4012G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65818769 | |||||||
chr5:65819019 | G | A | 2 | a0003c0005t0023g0060 a0003c0005t0023g0087 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1981-3762G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819019 | |||||||
chr5:65819175 | G | A | 175 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(172): Show |
187 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.1981-3606G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819175 | |||||||
chr5:65819190 | T | A | 1 | a0005c0009t0044g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1981-3591T>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819190 | |||||||
chr5:65819190 | T | C | 3 | a0001c0001t0002g0257 a0002c0004t0040g0310 a0002c0004t0043g0258 |
3 | HG02258.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-3591T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819190 | |||||||
chr5:65819437 | A | G | 1 | a0001c0001t0042g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1981-3344A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819437 | |||||||
chr5:65819460 | C | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(236): Show |
253 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.1981-3321C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819460 | |||||||
chr5:65819525 | G | A | 2 | a0002c0004t0016g0088 a0002c0016t0034g0256 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1981-3256G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819525 | |||||||
chr5:65819721 | A | G | 171 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(168): Show |
183 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.1981-3060A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65819721 | |||||||
chr5:65820011 | T | C | 1 | a0001c0002t0001g0209 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1981-2770T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820011 | |||||||
chr5:65820061 | C | A | 1 | a0003c0005t0023g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1981-2720C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820061 | |||||||
chr5:65820261 | A | G | 222 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(219): Show |
236 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.1981-2520A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820261 | |||||||
chr5:65820290 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(172): Show |
187 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.1981-2491C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820290 | |||||||
chr5:65820716 | G | GT | 7 | a0001c0001t0005g0261 a0001c0001t0019g0019 a0001c0002t0001g0100 others(4): Show |
8 | HG01109.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1981-2056dupT | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820716 | ||||||
chr5:65820718 | T | C | 6 | a0001c0001t0009g0024 a0001c0001t0009g0027 a0001c0001t0009g0068 others(3): Show |
6 | HG01070.hp2 HG01169.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-2063T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820718 | |||||||
chr5:65820722 | T | G | 1 | a0001c0007t0018g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1981-2059T>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820722 | |||||||
chr5:65820722 | T | TTTTG | 85 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(82): Show |
88 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1981-2043_1981-204 others(8): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820722 | ||||||
chr5:65820745 | C | T | 3 | a0004c0006t0001g0009 a0004c0006t0001g0101 a0004c0006t0001g0107 |
4 | HG02451.hp1 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-2036C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820745 | |||||||
chr5:65820746 | G | A | 1 | a0002c0016t0034g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1981-2035G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820746 | |||||||
chr5:65820799 | T | C | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1982T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820799 | |||||||
chr5:65820800 | G | T | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1981G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820800 | |||||||
chr5:65820804 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1977G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820804 | |||||||
chr5:65820899 | C | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1882C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820899 | |||||||
chr5:65820900 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(210): Show |
227 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1981-1881A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820900 | |||||||
chr5:65820962 | AC | A | 310 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(307): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1981-1815delC | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65820962 | ||||||
chr5:65820965 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1816C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65820965 | |||||||
chr5:65821042 | CA | C | 6 | a0001c0001t0039g0151 a0002c0004t0016g0061 a0002c0004t0016g0063 others(3): Show |
6 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1981-1723delA | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65821042 | ||||||
chr5:65821069 | A | C | 42 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0001g0156 others(39): Show |
44 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1981-1712A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821069 | |||||||
chr5:65821098 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1683G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821098 | |||||||
chr5:65821103 | A | T | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1678A>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821103 | |||||||
chr5:65821104 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1677G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821104 | |||||||
chr5:65821122 | G | T | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1659G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821122 | |||||||
chr5:65821125 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1656A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821125 | |||||||
chr5:65821259 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0003g0054 a0001c0001t0003g0055 others(1): Show |
4 | HG01081.hp2 HG01978.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-1522T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821259 | |||||||
chr5:65821293 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1981-1488T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821293 | |||||||
chr5:65821561 | CTT | C | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-1218_1981-121 others(6): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65821561 | ||||||
chr5:65821580 | G | T | 3 | a0001c0001t0005g0122 a0001c0001t0005g0230 a0001c0001t0005g0232 |
3 | NA18973.hp1 NA18994.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1981-1201G>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821580 | |||||||
chr5:65821599 | A | C | 2 | a0002c0004t0016g0061 a0002c0004t0016g0063 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1981-1182A>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821599 | |||||||
chr5:65821606 | C | T | 1 | a0004c0006t0029g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1981-1175C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821606 | |||||||
chr5:65821807 | C | A | 4 | a0002c0004t0016g0061 a0002c0004t0016g0063 a0002c0004t0016g0088 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-974C>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821807 | |||||||
chr5:65821943 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1981-838T>C | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65821943 | |||||||
chr5:65822185 | C | T | 1 | a0002c0003t0017g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1981-596C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822185 | |||||||
chr5:65822281 | C | T | 1 | a0001c0001t0005g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1981-500C>T | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822281 | |||||||
chr5:65822357 | ACCATTTG others(7): Show |
A | 3 | a0001c0001t0032g0220 a0001c0001t0033g0218 a0001c0001t0051g0298 |
3 | HG02451.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1981-419_1981-406d others(16): Show |
NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 65822357 | ||||||
chr5:65822584 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-197G>A | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822584 | |||||||
chr5:65822678 | A | G | 1 | a0001c0002t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1981-103A>G | NLN | ENSG00000123213.23 | transcript | ENST00000380985.10 | protein_coding | 12/12 | chr5 | 65822678 |