Item | Value |
---|---|
geneid | 23731 |
ensemblid | ENSG00000106771.13 |
hgncid | 1363 |
symbol | TMEM245 |
name | transmembrane protein 245 |
refseq_nuc | NM_032012.4 |
refseq_prot | NP_114401.2 |
ensembl_nuc | ENST00000374586.8 |
ensembl_prot | ENSP00000363714.3 |
mane_status | MANE Select |
chr | chr9 |
start | 109015135 |
end | 109119947 |
strand | - |
ver | v1.2 |
region | chr9:109015135-109119947 |
region5000 | chr9:109010135-109124947 |
regionname0 | TMEM245_chr9_109015135_109119947 |
regionname5000 | TMEM245_chr9_109010135_109124947 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 879 | 270 | 64 | 45 | 123 | 5 | 31 | 97 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0002 | 0/0 | 879 | 75 | 0 | 23 | 43 | 4 | 5 | 35 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0003 | 0/0 | 879 | 40 | 22 | 4 | 0 | 3 | 11 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0004 | 0/0 | 879 | 31 | 0 | 0 | 30 | 0 | 1 | 24 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0005 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0006 | 0/0 | 879 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0007 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
a0008 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | MADGG others(874): Show |
chr9 | 109010135 | 109124947 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2637 | 228 | 52 | 39 | 108 | 4 | 23 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0005 | 0/0 | 2637 | 15 | 0 | 2 | 13 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0006 | 0/0 | 2637 | 13 | 12 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0007 | 0/0 | 2637 | 8 | 0 | 0 | 0 | 1 | 7 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0009 | 0/0 | 2637 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0013 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0015 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0001c0016 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0002c0002 | 0/0 | 2637 | 75 | 0 | 23 | 43 | 4 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0003c0004 | 0/0 | 2637 | 30 | 14 | 2 | 0 | 3 | 11 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0003c0008 | 0/0 | 2637 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0003c0012 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0003c0017 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0003c0018 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0004c0003 | 0/0 | 2637 | 31 | 0 | 0 | 30 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0005c0011 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0006c0010 | 0/0 | 2637 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0007c0014 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 | ||
a0008c0019 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ATGGC others(2632): Show |
chr9 | 109010135 | 109124947 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 8001 | 16 | 0 | 11 | 0 | 2 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0003 | 0/0 | 8000 | 27 | 1 | 5 | 20 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0004 | 0/0 | 7999 | 27 | 1 | 5 | 18 | 0 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0005 | 0/0 | 7999 | 28 | 2 | 7 | 17 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0006 | 0/0 | 8001 | 19 | 0 | 0 | 15 | 1 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0007 | 0/0 | 7999 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0008 | 1/0 | 7999 | 11 | 7 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0009 | 0/0 | 8001 | 11 | 2 | 0 | 9 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0011 | 0/0 | 7990 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7985): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0012 | 0/0 | 8002 | 6 | 3 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0013 | 0/0 | 8000 | 6 | 1 | 0 | 3 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0014 | 0/0 | 8000 | 5 | 3 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0015 | 0/0 | 8002 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0019 | 0/0 | 8001 | 4 | 2 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0020 | 0/0 | 7999 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0022 | 0/0 | 8000 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0023 | 0/0 | 7999 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0025 | 0/0 | 8001 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0026 | 0/0 | 7998 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0027 | 0/0 | 8000 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0028 | 0/0 | 8002 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0032 | 0/0 | 8001 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0033 | 0/0 | 8000 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0034 | 0/0 | 8000 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0035 | 0/0 | 7999 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0036 | 0/0 | 8001 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0037 | 0/0 | 8002 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0038 | 0/0 | 8001 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0039 | 0/0 | 8000 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0040 | 0/0 | 8000 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0043 | 0/0 | 8000 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0045 | 0/0 | 7995 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0046 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7986): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0048 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0049 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0051 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0052 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0053 | 0/0 | 7999 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0054 | 0/0 | 7999 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0055 | 0/0 | 8000 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0056 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0057 | 0/0 | 8001 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0058 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0059 | 0/0 | 8001 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0065 | 0/0 | 7999 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0069 | 0/0 | 7999 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0070 | 0/1 | 7997 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7992): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0073 | 0/0 | 7990 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7985): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0074 | 0/0 | 7998 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0075 | 0/0 | 7998 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0076 | 0/0 | 7994 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7989): Show |
chr9 | 109010135 | 109124947 |
a0001c0001t0084 | 0/0 | 8001 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0001c0005t0003 | 0/0 | 8000 | 11 | 0 | 2 | 9 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0005t0023 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0005t0024 | 0/0 | 8000 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0011 | 0/0 | 7990 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7985): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0030 | 0/0 | 7994 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7989): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0041 | 0/0 | 7993 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7988): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0046 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7986): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0060 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0061 | 0/0 | 7994 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7989): Show |
chr9 | 109010135 | 109124947 |
a0001c0006t0072 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0001c0007t0004 | 0/0 | 7999 | 6 | 0 | 0 | 0 | 1 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0007t0026 | 0/0 | 7998 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0001c0007t0050 | 0/0 | 7999 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0009t0017 | 0/0 | 7999 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0013t0064 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0001c0015t0004 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0001c0016t0012 | 0/0 | 8002 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0001 | 0/0 | 7995 | 49 | 0 | 15 | 27 | 2 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0002 | 0/0 | 8001 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0010 | 0/0 | 7995 | 9 | 0 | 4 | 5 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0018 | 0/0 | 7996 | 5 | 0 | 1 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7991): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0021 | 0/0 | 7996 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7991): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0047 | 0/0 | 7995 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0077 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0078 | 0/0 | 7995 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0079 | 0/0 | 7994 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7989): Show |
chr9 | 109010135 | 109124947 |
a0002c0002t0080 | 0/0 | 7995 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0002 | 0/0 | 8001 | 3 | 0 | 0 | 0 | 0 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0007 | 0/0 | 7999 | 14 | 8 | 2 | 0 | 1 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0017 | 0/0 | 7999 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0031 | 0/0 | 8000 | 3 | 0 | 0 | 0 | 0 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0042 | 0/0 | 8000 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0044 | 0/0 | 7999 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0062 | 0/0 | 8001 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0071 | 0/0 | 7998 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7993): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0081 | 0/0 | 8001 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0003c0004t0083 | 0/0 | 7999 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0003c0008t0016 | 0/0 | 7996 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7991): Show |
chr9 | 109010135 | 109124947 |
a0003c0008t0067 | 0/0 | 7995 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0003c0008t0068 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0003c0012t0063 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7991): Show |
chr9 | 109010135 | 109124947 |
a0003c0017t0082 | 0/0 | 8001 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0003c0018t0066 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
a0004c0003t0002 | 0/0 | 8001 | 25 | 0 | 0 | 25 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7996): Show |
chr9 | 109010135 | 109124947 |
a0004c0003t0015 | 0/0 | 8002 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7997): Show |
chr9 | 109010135 | 109124947 |
a0004c0003t0029 | 0/0 | 8000 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0005c0011t0007 | 0/0 | 7999 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7994): Show |
chr9 | 109010135 | 109124947 |
a0006c0010t0003 | 0/0 | 8000 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0007c0014t0040 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7995): Show |
chr9 | 109010135 | 109124947 |
a0008c0019t0001 | 0/0 | 7995 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | ACCGC others(7990): Show |
chr9 | 109010135 | 109124947 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0008g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0011g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0011g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0015g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0015g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0019g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0019g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0019g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0019g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0020g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0020g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0020g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0022g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0023g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0025g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0025g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0025g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0026g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0026g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0027g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0027g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0027g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0028g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0028g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0028g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0032g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0032g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0033g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0033g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0034g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0034g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0035g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0035g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0036g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0036g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0037g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0037g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0038g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0038g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0039g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0039g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0040g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0043g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0043g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0045g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0045g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0046g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0048g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0049g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0051g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0052g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0053g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0054g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0055g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0056g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0057g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0058g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0059g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0065g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0069g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0070g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0073g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0074g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0075g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0076g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0001t0084g0420 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0023g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0024g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0005t0024g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0030g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0030g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0030g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0041g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0041g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0046g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0060g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0061g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0006t0072g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0026g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0007t0050g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0009t0017g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0009t0017g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0013t0064g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0015t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0001c0016t0012g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0415 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0001g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0002g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0002g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0010g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0018g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0018g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0018g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0018g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0018g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0021g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0021g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0021g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0021g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0047g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0047g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0077g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0078g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0079g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0002c0002t0080g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0017g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0017g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0031g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0031g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0031g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0042g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0042g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0044g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0044g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0062g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0071g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0081g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0004t0083g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0016g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0016g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0016g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0067g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0008t0068g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0012t0063g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0017t0082g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0003c0018t0066g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0015g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0015g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0029g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0029g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0004c0003t0029g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0005c0011t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0005c0011t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0006c0010t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0006c0010t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0007c0014t0040g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
a0008c0019t0001g0406 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0359 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00099 | hp2 | a0003 | c0004 | t0007 | g0329 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0030 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00408 | hp1 | a0004 | c0003 | t0002 | g0073 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00408 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0376 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00609 | hp2 | a0001 | c0001 | t0009 | g0107 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00621 | hp1 | a0002 | c0002 | t0018 | g0350 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00621 | hp2 | a0004 | c0003 | t0002 | g0037 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00639 | hp1 | a0007 | c0014 | t0040 | g0242 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00639 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00733 | hp1 | a0003 | c0008 | t0016 | g0308 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0390 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0364 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG00741 | hp2 | a0008 | c0019 | t0001 | g0406 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0366 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01081 | hp2 | a0001 | c0001 | t0014 | g0248 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0395 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01106 | hp1 | a0003 | c0004 | t0007 | g0340 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01109 | hp1 | a0003 | c0008 | t0067 | g0306 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01109 | hp2 | a0001 | c0013 | t0064 | g0023 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0410 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0409 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01175 | hp2 | a0002 | c0002 | t0018 | g0396 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0393 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0164 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0277 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01243 | hp2 | a0001 | c0001 | t0045 | g0174 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0187 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01255 | hp2 | a0001 | c0001 | t0084 | g0420 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01256 | hp2 | a0001 | c0001 | t0075 | g0156 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0347 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01261 | hp1 | a0001 | c0006 | t0030 | g0290 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0400 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0394 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0345 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01358 | hp2 | a0003 | c0004 | t0007 | g0341 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0391 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01361 | hp2 | a0001 | c0001 | t0015 | g0191 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01433 | hp1 | a0001 | c0009 | t0017 | g0002 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01433 | hp2 | a0002 | c0002 | t0010 | g0381 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01496 | hp1 | a0001 | c0009 | t0017 | g0002 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0371 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01515 | hp2 | a0003 | c0004 | t0017 | g0325 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01516 | hp2 | a0002 | c0002 | t0047 | g0360 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01517 | hp1 | a0003 | c0004 | t0017 | g0324 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01517 | hp2 | a0002 | c0002 | t0047 | g0358 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01884 | hp1 | a0001 | c0006 | t0046 | g0285 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01884 | hp2 | a0001 | c0001 | t0039 | g0044 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01891 | hp2 | a0001 | c0001 | t0057 | g0118 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01952 | hp1 | a0001 | c0001 | t0053 | g0197 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0348 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01978 | hp1 | a0002 | c0002 | t0077 | g0344 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01978 | hp2 | a0001 | c0005 | t0003 | g0012 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02004 | hp1 | a0002 | c0002 | t0010 | g0355 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02015 | hp2 | a0001 | c0005 | t0023 | g0013 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0377 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02040 | hp1 | a0001 | c0005 | t0024 | g0017 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02055 | hp1 | a0001 | c0001 | t0076 | g0083 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02055 | hp2 | a0001 | c0001 | t0019 | g0269 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0354 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02056 | hp2 | a0004 | c0003 | t0002 | g0038 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02071 | hp1 | a0001 | c0001 | t0013 | g0230 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02074 | hp2 | a0001 | c0001 | t0013 | g0229 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02080 | hp1 | a0002 | c0002 | t0021 | g0386 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02080 | hp2 | a0004 | c0003 | t0002 | g0069 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0134 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02129 | hp2 | a0002 | c0002 | t0010 | g0402 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02132 | hp2 | a0001 | c0001 | t0009 | g0112 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02145 | hp1 | a0003 | c0008 | t0016 | g0305 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02145 | hp2 | a0001 | c0001 | t0025 | g0184 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02148 | hp1 | a0002 | c0002 | t0010 | g0389 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | CDX | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0403 | EAS | CDX | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0272 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02257 | hp2 | a0003 | c0008 | t0016 | g0310 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02273 | hp2 | a0001 | c0005 | t0003 | g0019 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02293 | hp1 | a0001 | c0001 | t0051 | g0244 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0349 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02300 | hp2 | a0002 | c0002 | t0010 | g0379 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0275 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02451 | hp2 | a0003 | c0004 | t0007 | g0318 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02572 | hp1 | a0001 | c0006 | t0030 | g0292 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02572 | hp2 | a0001 | c0001 | t0034 | g0173 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0154 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02615 | hp1 | a0001 | c0006 | t0011 | g0281 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02615 | hp2 | a0003 | c0004 | t0083 | g0332 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02622 | hp1 | a0001 | c0001 | t0034 | g0158 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02622 | hp2 | a0001 | c0001 | t0022 | g0005 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0163 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02630 | hp2 | a0003 | c0004 | t0042 | g0314 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02647 | hp1 | a0001 | c0001 | t0048 | g0006 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02647 | hp2 | a0001 | c0006 | t0011 | g0280 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02698 | hp1 | a0001 | c0001 | t0069 | g0128 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02698 | hp2 | a0001 | c0001 | t0040 | g0031 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02717 | hp1 | a0001 | c0001 | t0022 | g0003 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02717 | hp2 | a0003 | c0004 | t0007 | g0317 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02723 | hp1 | a0001 | c0001 | t0035 | g0271 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0357 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02735 | hp2 | a0001 | c0007 | t0004 | g0299 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02738 | hp1 | a0003 | c0004 | t0031 | g0331 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02738 | hp2 | a0001 | c0001 | t0013 | g0273 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0234 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02886 | hp1 | a0003 | c0004 | t0044 | g0319 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02895 | hp1 | a0005 | c0011 | t0007 | g0339 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02895 | hp2 | a0001 | c0006 | t0011 | g0282 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02922 | hp1 | a0003 | c0012 | t0063 | g0022 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02965 | hp1 | a0003 | c0004 | t0007 | g0315 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02970 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0233 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03017 | hp1 | a0003 | c0004 | t0007 | g0326 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03041 | hp1 | a0003 | c0004 | t0007 | g0343 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0278 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03098 | hp1 | a0001 | c0006 | t0060 | g0291 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03098 | hp2 | a0001 | c0001 | t0038 | g0172 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03130 | hp1 | a0003 | c0004 | t0044 | g0320 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03130 | hp2 | a0001 | c0001 | t0058 | g0119 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03139 | hp1 | a0003 | c0004 | t0007 | g0316 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03139 | hp2 | a0001 | c0001 | t0014 | g0183 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03195 | hp1 | a0001 | c0001 | t0065 | g0029 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03195 | hp2 | a0003 | c0008 | t0016 | g0304 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03209 | hp1 | a0001 | c0001 | t0022 | g0004 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03209 | hp2 | a0001 | c0001 | t0039 | g0033 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03225 | hp1 | a0001 | c0006 | t0011 | g0283 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03225 | hp2 | a0001 | c0001 | t0045 | g0176 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0382 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03239 | hp2 | a0003 | c0004 | t0007 | g0330 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03453 | hp1 | a0003 | c0004 | t0062 | g0335 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03453 | hp2 | a0003 | c0018 | t0066 | g0307 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03486 | hp1 | a0003 | c0008 | t0016 | g0309 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03486 | hp2 | a0001 | c0001 | t0038 | g0169 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0383 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03490 | hp2 | a0001 | c0007 | t0026 | g0295 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03492 | hp1 | a0001 | c0007 | t0004 | g0300 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03516 | hp1 | a0001 | c0001 | t0025 | g0198 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03516 | hp2 | a0001 | c0001 | t0056 | g0104 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03540 | hp2 | a0005 | c0011 | t0007 | g0338 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0167 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03654 | hp1 | a0001 | c0001 | t0013 | g0247 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03654 | hp2 | a0003 | c0004 | t0002 | g0321 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03669 | hp1 | a0003 | c0004 | t0081 | g0342 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03669 | hp2 | a0001 | c0007 | t0004 | g0294 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03688 | hp2 | a0003 | c0004 | t0002 | g0322 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03704 | hp1 | a0001 | c0007 | t0050 | g0296 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03704 | hp2 | a0003 | c0004 | t0071 | g0328 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03710 | hp1 | a0003 | c0004 | t0007 | g0336 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0362 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03831 | hp2 | a0003 | c0004 | t0031 | g0327 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03834 | hp1 | a0001 | c0007 | t0004 | g0301 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0100 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03927 | hp1 | a0004 | c0003 | t0015 | g0061 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03942 | hp1 | a0001 | c0001 | t0015 | g0050 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG03942 | hp2 | a0001 | c0001 | t0008 | g0171 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04115 | hp1 | a0001 | c0001 | t0028 | g0079 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04115 | hp2 | a0001 | c0009 | t0017 | g0302 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04184 | hp1 | a0003 | c0004 | t0002 | g0323 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04184 | hp2 | a0001 | c0001 | t0023 | g0252 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04199 | hp1 | a0003 | c0004 | t0031 | g0333 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04199 | hp2 | a0001 | c0001 | t0054 | g0192 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04204 | hp2 | a0001 | c0001 | t0036 | g0177 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG04228 | hp2 | a0001 | c0001 | t0019 | g0259 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18522 | hp1 | a0003 | c0004 | t0007 | g0312 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18522 | hp2 | a0003 | c0008 | t0068 | g0303 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18612 | hp2 | a0004 | c0003 | t0002 | g0054 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18747 | hp1 | a0004 | c0003 | t0029 | g0056 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0368 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0160 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18906 | hp2 | a0001 | c0006 | t0030 | g0289 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18939 | hp2 | a0004 | c0003 | t0002 | g0040 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18940 | hp2 | a0001 | c0001 | t0012 | g0115 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0375 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0404 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18943 | hp1 | a0004 | c0003 | t0002 | g0065 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18943 | hp2 | a0001 | c0001 | t0037 | g0114 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0372 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18944 | hp2 | a0004 | c0003 | t0002 | g0063 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18945 | hp1 | a0001 | c0005 | t0003 | g0014 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18945 | hp2 | a0004 | c0003 | t0002 | g0059 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18946 | hp1 | a0002 | c0002 | t0079 | g0416 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18946 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18948 | hp1 | a0001 | c0001 | t0027 | g0260 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18948 | hp2 | a0001 | c0001 | t0026 | g0224 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0365 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18949 | hp2 | a0001 | c0015 | t0004 | g0268 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18950 | hp2 | a0004 | c0003 | t0002 | g0270 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18951 | hp1 | a0004 | c0003 | t0002 | g0057 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18951 | hp2 | a0001 | c0001 | t0055 | g0103 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18954 | hp2 | a0004 | c0003 | t0002 | g0052 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0412 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18956 | hp2 | a0001 | c0001 | t0074 | g0138 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18957 | hp2 | a0001 | c0001 | t0020 | g0279 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0411 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18959 | hp2 | a0004 | c0003 | t0002 | g0071 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18961 | hp1 | a0002 | c0002 | t0010 | g0380 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18962 | hp1 | a0004 | c0003 | t0002 | g0041 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18963 | hp1 | a0001 | c0001 | t0012 | g0110 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0398 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18964 | hp1 | a0001 | c0001 | t0059 | g0109 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18965 | hp1 | a0001 | c0001 | t0027 | g0199 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18966 | hp1 | a0004 | c0003 | t0002 | g0058 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0397 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18967 | hp1 | a0002 | c0002 | t0018 | g0352 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18968 | hp1 | a0001 | c0001 | t0020 | g0132 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18968 | hp2 | a0002 | c0002 | t0021 | g0405 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18971 | hp2 | a0002 | c0002 | t0010 | g0399 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18972 | hp1 | a0004 | c0003 | t0015 | g0062 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0392 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18974 | hp1 | a0004 | c0003 | t0002 | g0072 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0384 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18975 | hp1 | a0001 | c0005 | t0003 | g0020 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18977 | hp1 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0387 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18979 | hp1 | a0001 | c0005 | t0003 | g0015 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18981 | hp1 | a0004 | c0003 | t0002 | g0055 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18982 | hp1 | a0004 | c0003 | t0015 | g0053 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18982 | hp2 | a0001 | c0001 | t0027 | g0211 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0413 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18985 | hp1 | a0001 | c0001 | t0020 | g0131 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18986 | hp1 | a0001 | c0001 | t0032 | g0254 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0408 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18988 | hp2 | a0002 | c0002 | t0080 | g0374 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18989 | hp1 | a0001 | c0005 | t0024 | g0018 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18990 | hp1 | a0001 | c0001 | t0043 | g0122 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0378 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18994 | hp1 | a0001 | c0001 | t0037 | g0116 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18995 | hp1 | a0002 | c0002 | t0078 | g0353 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18998 | hp2 | a0006 | c0010 | t0003 | g0025 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18999 | hp1 | a0001 | c0001 | t0013 | g0124 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18999 | hp2 | a0001 | c0001 | t0009 | g0108 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19000 | hp1 | a0001 | c0001 | t0028 | g0081 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19000 | hp2 | a0002 | c0002 | t0010 | g0401 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0417 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19003 | hp1 | a0001 | c0001 | t0009 | g0111 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19003 | hp2 | a0002 | c0002 | t0021 | g0373 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0415 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19005 | hp1 | a0004 | c0003 | t0002 | g0060 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0385 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19006 | hp1 | a0001 | c0001 | t0012 | g0178 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19006 | hp2 | a0002 | c0002 | t0018 | g0418 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0407 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19007 | hp2 | a0004 | c0003 | t0002 | g0064 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19010 | hp1 | a0001 | c0001 | t0026 | g0226 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19011 | hp1 | a0001 | c0005 | t0003 | g0009 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19030 | hp1 | a0001 | c0001 | t0025 | g0262 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19030 | hp2 | a0003 | c0004 | t0007 | g0313 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19043 | hp1 | a0001 | c0001 | t0046 | g0188 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19043 | hp2 | a0003 | c0017 | t0082 | g0311 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0370 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19057 | hp1 | a0001 | c0001 | t0032 | g0253 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19057 | hp2 | a0001 | c0016 | t0012 | g0293 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19060 | hp1 | a0001 | c0001 | t0019 | g0208 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19060 | hp2 | a0001 | c0005 | t0024 | g0011 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19064 | hp1 | a0002 | c0002 | t0010 | g0369 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19064 | hp2 | a0004 | c0003 | t0002 | g0075 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0414 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19066 | hp1 | a0001 | c0001 | t0036 | g0181 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19066 | hp2 | a0001 | c0005 | t0003 | g0007 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19070 | hp1 | a0004 | c0003 | t0002 | g0066 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0419 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19072 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19075 | hp1 | a0001 | c0001 | t0009 | g0113 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19075 | hp2 | a0001 | c0001 | t0043 | g0127 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19078 | hp1 | a0002 | c0002 | t0018 | g0356 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19078 | hp2 | a0001 | c0001 | t0028 | g0097 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19080 | hp1 | a0006 | c0010 | t0003 | g0024 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19080 | hp2 | a0004 | c0003 | t0002 | g0074 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19082 | hp1 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19082 | hp2 | a0001 | c0005 | t0003 | g0016 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19084 | hp1 | a0004 | c0003 | t0002 | g0070 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19084 | hp2 | a0001 | c0001 | t0023 | g0209 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19085 | hp1 | a0001 | c0001 | t0009 | g0102 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19085 | hp2 | a0002 | c0002 | t0021 | g0367 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19086 | hp1 | a0001 | c0005 | t0003 | g0010 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19086 | hp2 | a0004 | c0003 | t0029 | g0036 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19088 | hp1 | a0001 | c0005 | t0003 | g0008 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19088 | hp2 | a0004 | c0003 | t0002 | g0068 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19090 | hp1 | a0004 | c0003 | t0002 | g0067 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19240 | hp1 | a0001 | c0006 | t0041 | g0286 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA19240 | hp2 | a0001 | c0001 | t0049 | g0186 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0098 | EUR | TSI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20805 | hp2 | a0001 | c0007 | t0004 | g0298 | EUR | TSI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20905 | hp1 | a0001 | c0007 | t0004 | g0297 | SAS | GIH | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0388 | SAS | GIH | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0363 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02109 | hp1 | a0001 | c0006 | t0072 | g0284 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02109 | hp2 | a0001 | c0001 | t0052 | g0185 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02486 | hp1 | a0001 | c0001 | t0033 | g0159 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02486 | hp2 | a0001 | c0006 | t0041 | g0287 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02559 | hp1 | a0003 | c0004 | t0007 | g0337 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0200 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG06807 | hp1 | a0001 | c0001 | t0073 | g0276 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
HG06807 | hp2 | a0001 | c0001 | t0033 | g0165 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18955 | hp1 | a0004 | c0003 | t0029 | g0120 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA18955 | hp2 | a0001 | c0005 | t0003 | g0021 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20300 | hp1 | a0001 | c0001 | t0013 | g0237 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA20300 | hp2 | a0001 | c0006 | t0061 | g0288 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA21309 | hp1 | a0003 | c0004 | t0042 | g0334 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
homoSapiens | chm13v2 | a0001 | c0001 | t0070 | g0151 | REF | REF | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0245 | REF | REF | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:109015136 | T | G | 1 | a0002 | 1 | NA18995.hp1 | splice_region_variant | LOW | c.*5324A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | chr9 | 109015136 | |||||||
chr9:109036233 | T | C | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2372A>G | p.Asp791Gly | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/18 | 2406/7999 | 2372/2640 | 791/879 | chr9 | 109036233 | |||
chr9:109091132 | C | T | 1 | a0004 | 31 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(28): Show |
missense_variant | MODERATE | c.940G>A | p.Ala314Thr | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/18 | 974/7999 | 940/2640 | 314/879 | chr9 | 109091132 | |||
chr9:109108507 | G | A | 1 | a0005 | 2 | HG02895.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.643C>T | p.Arg215Cys | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/18 | 677/7999 | 643/2640 | 215/879 | chr9 | 109108507 | |||
chr9:109108521 | T | C | 1 | a0008 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.629A>G | p.Asn210Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/18 | 663/7999 | 629/2640 | 210/879 | chr9 | 109108521 | |||
chr9:109119576 | T | C | 2 | a0002 a0008 |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
missense_variant | MODERATE | c.338A>G | p.His113Arg | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 372/7999 | 338/2640 | 113/879 | chr9 | 109119576 | |||
chr9:109119834 | A | G | 1 | a0006 | 2 | NA18998.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.80T>C | p.Val27Ala | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 114/7999 | 80/2640 | 27/879 | chr9 | 109119834 | |||
chr9:109119887 | G | C | 4 | a0002 a0003 a0005 others(1): Show |
118 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(115): Show |
missense_variant | MODERATE | c.27C>G | p.Asp9Glu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 61/7999 | 27/2640 | 9/879 | chr9 | 109119887 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:109064522 | C | T | 1 | a0003c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1578G>A | p.Ala526Ala | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/18 | 1612/7999 | 1578/2640 | 526/879 | chr9 | 109064522 | |||
chr9:109087295 | G | A | 1 | a0003c0008 | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.1198C>T | p.Leu400Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/18 | 1232/7999 | 1198/2640 | 400/879 | chr9 | 109087295 | |||
chr9:109091133 | G | A | 1 | a0001c0015 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.939C>T | p.Ser313Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/18 | 973/7999 | 939/2640 | 313/879 | chr9 | 109091133 | |||
chr9:109106605 | G | A | 2 | a0002c0002 a0008c0019 |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
synonymous_variant | LOW | c.702C>T | p.Ser234Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/18 | 736/7999 | 702/2640 | 234/879 | chr9 | 109106605 | |||
chr9:109119466 | G | A | 1 | a0001c0006 | 13 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.448C>T | p.Leu150Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 482/7999 | 448/2640 | 150/879 | chr9 | 109119466 | |||
chr9:109119530 | G | C | 1 | a0001c0016 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.384C>G | p.Leu128Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 418/7999 | 384/2640 | 128/879 | chr9 | 109119530 | |||
chr9:109119553 | G | A | 1 | a0001c0007 | 8 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(5): Show |
synonymous_variant | LOW | c.361C>T | p.Leu121Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 395/7999 | 361/2640 | 121/879 | chr9 | 109119553 | |||
chr9:109119647 | T | C | 5 | a0001c0009 a0002c0002 a0003c0004 others(2): Show |
111 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(108): Show |
synonymous_variant | LOW | c.267A>G | p.Leu89Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 301/7999 | 267/2640 | 89/879 | chr9 | 109119647 | |||
chr9:109119872 | C | T | 1 | a0001c0013 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.42G>A | p.Arg14Arg | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 76/7999 | 42/2640 | 14/879 | chr9 | 109119872 | |||
chr9:109119890 | C | T | 2 | a0001c0005 a0003c0012 |
16 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(13): Show |
synonymous_variant | LOW | c.24G>A | p.Lys8Lys | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 58/7999 | 24/2640 | 8/879 | chr9 | 109119890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:109015183 | TATAA | T | 7 | a0001c0001t0045 a0001c0001t0076 a0003c0008t0016 others(4): Show |
12 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5273_*5276delTTAT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 5273 | chr9 | 109015183 | ||||||
chr9:109015236 | TTAGC | T | 9 | a0002c0002t0001 a0002c0002t0010 a0002c0002t0018 others(6): Show |
73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5220_*5223delGCTA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 5220 | chr9 | 109015236 | ||||||
chr9:109015705 | T | C | 1 | a0001c0001t0045 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4755A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4755 | chr9 | 109015705 | ||||||
chr9:109015735 | C | A | 13 | a0001c0001t0007 a0001c0001t0065 a0001c0009t0017 others(10): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4725G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4725 | chr9 | 109015735 | ||||||
chr9:109015740 | C | A | 1 | a0001c0001t0052 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4720G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4720 | chr9 | 109015740 | ||||||
chr9:109016196 | C | T | 2 | a0001c0001t0051 a0001c0001t0053 |
2 | HG01952.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4264G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4264 | chr9 | 109016196 | ||||||
chr9:109016207 | A | G | 1 | a0003c0004t0081 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4253T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4253 | chr9 | 109016207 | ||||||
chr9:109016418 | GA | G | 7 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0043 others(4): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4041delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4041 | chr9 | 109016418 | ||||||
chr9:109016546 | TA | T | 11 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0026 others(8): Show |
49 | HG00558.hp1 HG00735.hp1 HG01069.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3913delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3913 | chr9 | 109016546 | ||||||
chr9:109016548 | G | C | 11 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0026 others(8): Show |
49 | HG00558.hp1 HG00735.hp1 HG01069.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3912C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3912 | chr9 | 109016548 | ||||||
chr9:109016656 | GTGTTTTT | G | 6 | a0001c0001t0046 a0001c0006t0030 a0001c0006t0041 others(3): Show |
9 | HG01261.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3797_*3803delAAAA others(3): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3797 | chr9 | 109016656 | ||||||
chr9:109016656 | GTGTTTTT others(1): Show |
G | 3 | a0001c0001t0011 a0001c0001t0073 a0001c0006t0011 |
9 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3796_*3803delAAAA others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3796 | chr9 | 109016656 | ||||||
chr9:109016658 | GT | G | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
48 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3801delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3801 | chr9 | 109016658 | ||||||
chr9:109016658 | GTT | G | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
166 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*3800_*3801delAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3800 | chr9 | 109016658 | ||||||
chr9:109016658 | GTTT | G | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(21): Show |
113 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3799_*3801delAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3799 | chr9 | 109016658 | ||||||
chr9:109016658 | GTTTT | G | 15 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(12): Show |
29 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3798_*3801delAAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3798 | chr9 | 109016658 | ||||||
chr9:109016658 | GTTTTT | G | 11 | a0001c0001t0045 a0001c0001t0065 a0001c0001t0076 others(8): Show |
23 | HG01243.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3797_*3801delAAAA others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3797 | chr9 | 109016658 | ||||||
chr9:109016658 | GTTTTTT | G | 3 | a0003c0008t0016 a0003c0008t0067 a0003c0008t0068 |
6 | HG00733.hp1 HG01109.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3796_*3801delAAAA others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3796 | chr9 | 109016658 | ||||||
chr9:109016911 | A | G | 1 | a0003c0008t0067 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3549T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3549 | chr9 | 109016911 | ||||||
chr9:109016940 | G | GT | 7 | a0001c0001t0002 a0001c0001t0015 a0002c0002t0002 others(4): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3519dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3519 | chr9 | 109016940 | ||||||
chr9:109016940 | GT | G | 12 | a0001c0001t0007 a0001c0001t0065 a0003c0004t0007 others(9): Show |
30 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3519delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3519 | chr9 | 109016940 | ||||||
chr9:109016949 | T | C | 25 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0013 others(22): Show |
115 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3511A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3511 | chr9 | 109016949 | ||||||
chr9:109016967 | T | C | 7 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0040 others(4): Show |
27 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3493A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3493 | chr9 | 109016967 | ||||||
chr9:109017018 | A | T | 7 | a0001c0001t0045 a0001c0001t0076 a0003c0008t0016 others(4): Show |
12 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3442T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3442 | chr9 | 109017018 | ||||||
chr9:109017119 | T | A | 1 | a0001c0001t0075 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3341A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3341 | chr9 | 109017119 | ||||||
chr9:109017131 | C | A | 1 | a0001c0001t0035 | 2 | HG02257.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3329G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3329 | chr9 | 109017131 | ||||||
chr9:109017251 | G | T | 1 | a0001c0001t0069 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3209C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3209 | chr9 | 109017251 | ||||||
chr9:109017340 | A | G | 2 | a0003c0012t0063 a0003c0018t0066 |
2 | HG02922.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3120T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3120 | chr9 | 109017340 | ||||||
chr9:109017346 | G | A | 2 | a0002c0002t0010 a0002c0002t0078 |
10 | HG01433.hp2 HG02004.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3114C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3114 | chr9 | 109017346 | ||||||
chr9:109017473 | T | C | 1 | a0001c0001t0037 | 2 | NA18943.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2987A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2987 | chr9 | 109017473 | ||||||
chr9:109017541 | T | C | 1 | a0003c0004t0044 | 2 | HG02886.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2919A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2919 | chr9 | 109017541 | ||||||
chr9:109017568 | G | A | 2 | a0001c0001t0022 a0001c0001t0038 |
5 | HG02622.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2892C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2892 | chr9 | 109017568 | ||||||
chr9:109017632 | A | C | 1 | a0002c0002t0047 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2828T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2828 | chr9 | 109017632 | ||||||
chr9:109017656 | C | T | 1 | a0003c0017t0082 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2804G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2804 | chr9 | 109017656 | ||||||
chr9:109017879 | G | A | 1 | a0001c0001t0032 | 2 | NA18986.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2581C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2581 | chr9 | 109017879 | ||||||
chr9:109017980 | A | C | 1 | a0001c0001t0065 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2480T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2480 | chr9 | 109017980 | ||||||
chr9:109018149 | T | C | 1 | a0001c0001t0073 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2311A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2311 | chr9 | 109018149 | ||||||
chr9:109018240 | G | A | 1 | a0001c0001t0056 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2220C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2220 | chr9 | 109018240 | ||||||
chr9:109018290 | T | A | 1 | a0001c0001t0054 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2170A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2170 | chr9 | 109018290 | ||||||
chr9:109018381 | C | A | 5 | a0001c0001t0005 a0001c0001t0043 a0001c0001t0069 others(2): Show |
33 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2079G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2079 | chr9 | 109018381 | ||||||
chr9:109018613 | A | T | 2 | a0001c0006t0030 a0001c0006t0060 |
4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1847T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1847 | chr9 | 109018613 | ||||||
chr9:109018739 | C | CT | 9 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0043 others(6): Show |
41 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1720dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1720 | chr9 | 109018739 | ||||||
chr9:109018835 | A | T | 15 | a0001c0001t0011 a0001c0001t0046 a0001c0001t0073 others(12): Show |
28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1625T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1625 | chr9 | 109018835 | ||||||
chr9:109018872 | A | G | 15 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0019 others(12): Show |
67 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1588T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1588 | chr9 | 109018872 | ||||||
chr9:109018900 | A | AT | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(41): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1559dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | ||||||
chr9:109018900 | A | ATT | 18 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0013 others(15): Show |
66 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1558_*1559dupAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | ||||||
chr9:109018900 | A | ATTT | 7 | a0001c0001t0012 a0001c0001t0028 a0001c0001t0037 others(4): Show |
15 | HG02809.hp2 HG02886.hp2 HG02970.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1557_*1559dupAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | ||||||
chr9:109018900 | AT | A | 10 | a0001c0001t0011 a0001c0001t0046 a0001c0001t0073 others(7): Show |
16 | HG01243.hp1 HG01256.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1559delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | ||||||
chr9:109018956 | G | A | 2 | a0002c0002t0021 a0002c0002t0080 |
5 | HG02080.hp1 NA18968.hp2 NA18988.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1504C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1504 | chr9 | 109018956 | ||||||
chr9:109019004 | C | T | 8 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0036 others(5): Show |
25 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1456G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1456 | chr9 | 109019004 | ||||||
chr9:109019068 | C | T | 1 | a0001c0007t0050 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1392 | chr9 | 109019068 | ||||||
chr9:109019215 | G | A | 9 | a0002c0002t0001 a0002c0002t0010 a0002c0002t0018 others(6): Show |
73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1245 | chr9 | 109019215 | ||||||
chr9:109019253 | C | T | 1 | a0001c0001t0049 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1207G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1207 | chr9 | 109019253 | ||||||
chr9:109019281 | G | A | 1 | a0001c0005t0024 | 3 | HG02040.hp1 NA18989.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1179C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1179 | chr9 | 109019281 | ||||||
chr9:109019308 | A | T | 1 | a0003c0004t0081 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1152 | chr9 | 109019308 | ||||||
chr9:109019333 | T | A | 1 | a0001c0001t0033 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1127A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1127 | chr9 | 109019333 | ||||||
chr9:109019334 | C | A | 1 | a0001c0001t0033 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1126 | chr9 | 109019334 | ||||||
chr9:109019337 | T | C | 1 | a0001c0001t0033 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1123A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1123 | chr9 | 109019337 | ||||||
chr9:109019341 | C | T | 1 | a0001c0001t0033 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1119G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1119 | chr9 | 109019341 | ||||||
chr9:109019377 | T | C | 1 | a0003c0004t0081 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1083 | chr9 | 109019377 | ||||||
chr9:109019411 | A | T | 1 | a0001c0001t0036 | 2 | HG04204.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1049T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1049 | chr9 | 109019411 | ||||||
chr9:109019413 | G | T | 8 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0036 others(5): Show |
25 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1047C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1047 | chr9 | 109019413 | ||||||
chr9:109019499 | T | C | 10 | a0002c0002t0001 a0002c0002t0010 a0002c0002t0018 others(7): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 961 | chr9 | 109019499 | ||||||
chr9:109019509 | A | G | 9 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0023 others(6): Show |
55 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*951T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 951 | chr9 | 109019509 | ||||||
chr9:109019630 | G | A | 1 | a0003c0004t0081 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 830 | chr9 | 109019630 | ||||||
chr9:109019651 | G | C | 1 | a0001c0001t0027 | 3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*809C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 809 | chr9 | 109019651 | ||||||
chr9:109019769 | G | A | 1 | a0001c0001t0059 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 691 | chr9 | 109019769 | ||||||
chr9:109019798 | T | C | 1 | a0003c0017t0082 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 662 | chr9 | 109019798 | ||||||
chr9:109019839 | G | A | 1 | a0003c0004t0083 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 621 | chr9 | 109019839 | ||||||
chr9:109020251 | T | G | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(23): Show |
114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*209A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 209 | chr9 | 109020251 | ||||||
chr9:109020390 | G | A | 48 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(45): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*70C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 70 | chr9 | 109020390 | ||||||
chr9:109119928 | A | G | 2 | a0001c0001t0022 a0001c0001t0048 |
4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-15T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 15 | chr9 | 109119928 | ||||||
chr9:109119940 | G | C | 1 | a0001c0001t0084 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 27 | chr9 | 109119940 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:109020534 | T | G | 1 | a0001c0007t0004g0301 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2595-29A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020534 | |||||||
chr9:109020540 | A | G | 2 | a0001c0001t0020g0131 a0001c0001t0020g0132 |
2 | NA18968.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2595-35T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020540 | |||||||
chr9:109020587 | G | C | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-82C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020587 | |||||||
chr9:109020601 | T | C | 12 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2595-96A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020601 | |||||||
chr9:109020664 | T | C | 1 | a0001c0001t0003g0213 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2595-159A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020664 | |||||||
chr9:109020689 | G | A | 1 | a0001c0001t0006g0099 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2595-184C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020689 | |||||||
chr9:109020830 | G | A | 1 | a0003c0004t0031g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2595-325C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020830 | |||||||
chr9:109021132 | C | T | 1 | a0001c0001t0039g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2595-627G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021132 | |||||||
chr9:109021142 | C | A | 2 | a0002c0002t0001g0361 a0002c0002t0001g0364 |
2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.2595-637G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021142 | |||||||
chr9:109021223 | T | C | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2595-718A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021223 | |||||||
chr9:109021421 | A | G | 2 | a0001c0001t0009g0107 a0001c0001t0059g0109 |
2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2595-916T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021421 | |||||||
chr9:109021453 | C | T | 3 | a0001c0007t0004g0299 a0001c0007t0004g0300 a0001c0007t0026g0295 |
3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2595-948G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021453 | |||||||
chr9:109021491 | G | T | 177 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2595-986C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021491 | |||||||
chr9:109021495 | TTTTG | T | 140 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(137): Show |
140 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.2595-994_2595-991d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021495 | |||||||
chr9:109021495 | TTTTGTTT others(1): Show |
T | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-998_2595-991d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021495 | |||||||
chr9:109021503 | GTTTGTTT others(2): Show |
G | 4 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 others(1): Show |
4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2595-1007_2595-999 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021503 | |||||||
chr9:109021820 | A | C | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-1315T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021820 | |||||||
chr9:109021837 | G | A | 1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2595-1332C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021837 | |||||||
chr9:109021838 | A | G | 1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2595-1333T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021838 | |||||||
chr9:109021851 | A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2595-1346T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021851 | |||||||
chr9:109021877 | AAAGT | A | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-1376_2595-137 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021877 | |||||||
chr9:109022086 | T | C | 1 | a0003c0008t0016g0309 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2595-1581A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022086 | |||||||
chr9:109022141 | G | A | 1 | a0001c0001t0004g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2595-1636C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022141 | |||||||
chr9:109022152 | A | G | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2595-1647T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022152 | |||||||
chr9:109022167 | A | G | 2 | a0001c0001t0035g0271 a0001c0001t0035g0272 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2595-1662T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022167 | |||||||
chr9:109022289 | C | T | 1 | a0002c0002t0010g0380 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2595-1784G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022289 | |||||||
chr9:109022467 | T | TTATC | 66 | a0001c0001t0003g0201 a0001c0001t0003g0205 a0001c0001t0003g0249 others(63): Show |
66 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.2595-1966_2595-196 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | T | TTATCTAT others(1): Show |
155 | a0001c0001t0002g0001 a0001c0001t0002g0042 a0001c0001t0002g0043 others(152): Show |
156 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.2595-1970_2595-196 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | T | TTATCTAT others(5): Show |
69 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0049 others(66): Show |
69 | HG00609.hp2 HG00621.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.2595-1974_2595-196 others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | T | TTATCTAT others(9): Show |
19 | a0001c0001t0003g0251 a0001c0001t0004g0196 a0001c0001t0005g0144 others(16): Show |
19 | HG00099.hp1 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.2595-1978_2595-196 others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | T | TTATCTAT others(13): Show |
4 | a0002c0002t0001g0346 a0004c0003t0002g0040 a0004c0003t0002g0065 others(1): Show |
4 | HG01934.hp1 NA18939.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2595-1982_2595-196 others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | T | TTATCTAT others(17): Show |
1 | a0004c0003t0002g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2595-1986_2595-196 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | TTATC | T | 37 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(34): Show |
37 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.2595-1966_2595-196 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022467 | TTATCTAT others(1): Show |
T | 23 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0005t0003g0012 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2595-1970_2595-196 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | |||||||
chr9:109022692 | C | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-2187G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022692 | |||||||
chr9:109022712 | T | C | 1 | a0001c0006t0041g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2595-2207A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022712 | |||||||
chr9:109022882 | C | G | 1 | a0001c0001t0025g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2595-2377G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022882 | |||||||
chr9:109023354 | C | T | 1 | a0004c0003t0015g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2595-2849G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023354 | |||||||
chr9:109023390 | T | C | 1 | a0001c0001t0009g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2595-2885A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023390 | |||||||
chr9:109023598 | G | A | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2595-3093C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023598 | |||||||
chr9:109023601 | G | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2595-3096C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023601 | |||||||
chr9:109023605 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-3100G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023605 | |||||||
chr9:109023836 | C | CA | 15 | a0001c0001t0013g0273 a0001c0001t0019g0269 a0001c0001t0053g0197 others(12): Show |
16 | HG01109.hp2 HG01433.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2595-3332dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023836 | |||||||
chr9:109023836 | CA | C | 20 | a0001c0001t0006g0091 a0001c0001t0011g0189 a0001c0001t0011g0275 others(17): Show |
20 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2595-3332delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023836 | |||||||
chr9:109023926 | C | A | 6 | a0001c0001t0009g0106 a0001c0001t0009g0108 a0001c0001t0009g0111 others(3): Show |
6 | HG02132.hp2 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2595-3421G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023926 | |||||||
chr9:109024075 | G | T | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-3570C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024075 | |||||||
chr9:109024168 | A | G | 404 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(401): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.2595-3663T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024168 | |||||||
chr9:109024315 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-3810G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024315 | |||||||
chr9:109024341 | T | G | 8 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(5): Show |
8 | HG01192.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2595-3836A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024341 | |||||||
chr9:109024422 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2595-3917G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024422 | |||||||
chr9:109024541 | G | A | 2 | a0001c0001t0004g0193 a0001c0001t0004g0218 |
2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2595-4036C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024541 | |||||||
chr9:109024544 | T | C | 10 | a0001c0001t0065g0029 a0003c0004t0007g0312 a0003c0004t0007g0313 others(7): Show |
10 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2595-4039A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024544 | |||||||
chr9:109024798 | G | C | 5 | a0001c0001t0005g0136 a0001c0001t0005g0153 a0001c0001t0020g0131 others(2): Show |
5 | NA18939.hp1 NA18941.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.2595-4293C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024798 | |||||||
chr9:109024845 | A | G | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-4340T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024845 | |||||||
chr9:109025310 | G | A | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2595-4805C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025310 | |||||||
chr9:109025395 | C | G | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-4890G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025395 | |||||||
chr9:109025872 | T | A | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2595-5367A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025872 | |||||||
chr9:109025888 | T | C | 53 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.2595-5383A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025888 | |||||||
chr9:109025948 | T | C | 226 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(223): Show |
227 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(224): Show |
intron_variant | MODIFIER | c.2595-5443A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025948 | |||||||
chr9:109025963 | G | A | 2 | a0001c0001t0009g0113 a0001c0001t0012g0110 |
2 | NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2595-5458C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025963 | |||||||
chr9:109026027 | T | C | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-5522A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026027 | |||||||
chr9:109026226 | A | AAC | 11 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0278 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2595-5723_2595-572 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026226 | |||||||
chr9:109026278 | T | C | 36 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(33): Show |
36 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2595-5773A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026278 | |||||||
chr9:109026297 | A | G | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-5792T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026297 | |||||||
chr9:109026300 | A | G | 53 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.2595-5795T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026300 | |||||||
chr9:109026411 | T | G | 1 | a0001c0001t0005g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2595-5906A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026411 | |||||||
chr9:109026420 | G | A | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2595-5915C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026420 | |||||||
chr9:109026420 | G | C | 3 | a0002c0002t0001g0365 a0002c0002t0001g0397 a0002c0002t0001g0398 |
3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2595-5915C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026420 | |||||||
chr9:109026517 | G | A | 1 | a0003c0004t0083g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2595-6012C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026517 | |||||||
chr9:109026579 | G | GA | 11 | a0001c0001t0011g0277 a0001c0001t0076g0083 a0003c0008t0016g0304 others(8): Show |
11 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2595-6075dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026579 | |||||||
chr9:109026599 | G | C | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-6094C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026599 | |||||||
chr9:109026678 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2595-6173G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026678 | |||||||
chr9:109026695 | T | C | 193 | a0001c0001t0003g0250 a0001c0001t0005g0101 a0001c0001t0005g0121 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.2595-6190A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026695 | |||||||
chr9:109026724 | G | A | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-6219C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026724 | |||||||
chr9:109026726 | T | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-6221A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026726 | |||||||
chr9:109026996 | G | A | 1 | a0004c0003t0002g0074 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2594+6311C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026996 | |||||||
chr9:109027058 | G | T | 1 | a0001c0001t0028g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2594+6249C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027058 | |||||||
chr9:109027239 | T | TAAAGAGC others(303): Show |
1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+6067_2594+606 others(314): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027239 | |||||||
chr9:109027340 | GT | G | 140 | a0001c0001t0003g0250 a0001c0001t0007g0030 a0001c0001t0011g0189 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2594+5966delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027340 | |||||||
chr9:109027347 | T | C | 1 | a0001c0001t0037g0114 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2594+5960A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027347 | |||||||
chr9:109027526 | CAGG | C | 4 | a0002c0002t0001g0368 a0002c0002t0001g0403 a0002c0002t0001g0404 others(1): Show |
4 | HG02165.hp2 NA18747.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594+5778_2594+578 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027526 | |||||||
chr9:109027534 | T | C | 53 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.2594+5773A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027534 | |||||||
chr9:109027678 | C | CT | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2594+5628dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027678 | |||||||
chr9:109028152 | T | C | 178 | a0001c0001t0003g0250 a0001c0001t0005g0101 a0001c0001t0005g0121 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2594+5155A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028152 | |||||||
chr9:109028221 | G | A | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2594+5086C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028221 | |||||||
chr9:109028269 | G | A | 2 | a0003c0004t0007g0340 a0003c0004t0071g0328 |
2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2594+5038C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028269 | |||||||
chr9:109028307 | G | A | 27 | a0001c0001t0005g0129 a0001c0001t0005g0152 a0001c0001t0009g0102 others(24): Show |
27 | HG00609.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.2594+5000C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028307 | |||||||
chr9:109028382 | T | A | 404 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(401): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.2594+4925A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028382 | |||||||
chr9:109028450 | A | G | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+4857T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028450 | |||||||
chr9:109028454 | C | CA | 132 | a0001c0001t0003g0250 a0001c0001t0005g0101 a0001c0001t0005g0121 others(129): Show |
133 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2594+4852dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028454 | |||||||
chr9:109028454 | CA | C | 204 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(201): Show |
205 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.2594+4852delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028454 | |||||||
chr9:109028579 | C | T | 30 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(27): Show |
30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2594+4728G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028579 | |||||||
chr9:109028732 | C | T | 5 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+4575G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028732 | |||||||
chr9:109028952 | G | A | 1 | a0001c0005t0024g0011 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2594+4355C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028952 | |||||||
chr9:109028981 | G | A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+4326C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028981 | |||||||
chr9:109029035 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+4272G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029035 | |||||||
chr9:109029132 | A | G | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2594+4175T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029132 | |||||||
chr9:109029368 | T | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2594+3939A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029368 | |||||||
chr9:109029430 | A | G | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2594+3877T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029430 | |||||||
chr9:109029432 | T | A | 1 | a0001c0001t0036g0181 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2594+3875A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029432 | |||||||
chr9:109029443 | T | A | 1 | a0002c0002t0079g0416 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2594+3864A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029443 | |||||||
chr9:109029493 | A | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3814T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029493 | |||||||
chr9:109029561 | G | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3746C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029561 | |||||||
chr9:109029633 | G | A | 1 | a0001c0001t0039g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2594+3674C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029633 | |||||||
chr9:109029712 | T | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(49): Show |
53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2594+3595A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029712 | |||||||
chr9:109029828 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3479G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029828 | |||||||
chr9:109029883 | G | A | 1 | a0003c0004t0007g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2594+3424C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029883 | |||||||
chr9:109029886 | A | G | 1 | a0001c0001t0012g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2594+3421T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029886 | |||||||
chr9:109029951 | T | C | 32 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(29): Show |
32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2594+3356A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029951 | |||||||
chr9:109029959 | G | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2594+3348C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029959 | |||||||
chr9:109030064 | T | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3243A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030064 | |||||||
chr9:109030106 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+3201G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030106 | |||||||
chr9:109030130 | A | C | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594+3177T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030130 | |||||||
chr9:109030154 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3153G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030154 | |||||||
chr9:109030244 | AGTCCTTA others(2): Show |
A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+3054_2594+306 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030244 | |||||||
chr9:109030286 | T | C | 25 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(22): Show |
25 | HG00558.hp1 HG02040.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2594+3021A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030286 | |||||||
chr9:109030331 | A | AT | 32 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(29): Show |
32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2594+2975dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030331 | |||||||
chr9:109030360 | T | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2594+2947A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030360 | |||||||
chr9:109030408 | A | G | 5 | a0001c0001t0003g0250 a0002c0002t0001g0371 a0002c0002t0001g0382 others(2): Show |
5 | HG00735.hp2 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2594+2899T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030408 | |||||||
chr9:109030614 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2594+2693C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030614 | |||||||
chr9:109030649 | G | C | 2 | a0006c0010t0003g0024 a0006c0010t0003g0025 |
2 | NA18998.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2594+2658C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030649 | |||||||
chr9:109030669 | T | C | 1 | a0006c0010t0003g0024 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2594+2638A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030669 | |||||||
chr9:109030782 | C | A | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2594+2525G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030782 | |||||||
chr9:109030993 | C | T | 3 | a0001c0001t0076g0083 a0003c0012t0063g0022 a0003c0018t0066g0307 |
3 | HG02055.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2594+2314G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030993 | |||||||
chr9:109031049 | A | G | 2 | a0001c0001t0033g0159 a0001c0001t0033g0165 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2594+2258T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031049 | |||||||
chr9:109031307 | G | C | 38 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2594+2000C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031307 | |||||||
chr9:109031327 | A | T | 405 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(402): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2594+1980T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031327 | |||||||
chr9:109031439 | T | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2594+1868A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031439 | |||||||
chr9:109031486 | C | T | 2 | a0001c0001t0006g0091 a0001c0001t0006g0175 |
2 | HG02129.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2594+1821G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031486 | |||||||
chr9:109031512 | G | T | 1 | a0001c0001t0004g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2594+1795C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031512 | |||||||
chr9:109031673 | G | A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+1634C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031673 | |||||||
chr9:109031697 | T | C | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+1610A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031697 | |||||||
chr9:109031987 | T | G | 1 | a0001c0001t0013g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2594+1320A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031987 | |||||||
chr9:109032190 | T | C | 30 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(27): Show |
30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2594+1117A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032190 | |||||||
chr9:109032199 | G | A | 1 | a0001c0001t0039g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2594+1108C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032199 | |||||||
chr9:109032225 | C | T | 1 | a0002c0002t0001g0351 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2594+1082G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032225 | |||||||
chr9:109032303 | A | G | 1 | a0003c0012t0063g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2594+1004T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032303 | |||||||
chr9:109032365 | C | CT | 14 | a0001c0001t0002g0032 a0001c0001t0008g0163 a0001c0001t0039g0044 others(11): Show |
14 | HG00738.hp2 HG01884.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2594+941dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTT | 24 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0045 others(21): Show |
25 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594+940_2594+941d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTT | 31 | a0001c0001t0002g0049 a0001c0001t0002g0051 a0001c0001t0003g0232 others(28): Show |
31 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.2594+939_2594+941d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTT | 34 | a0001c0001t0003g0202 a0001c0001t0003g0250 a0001c0001t0003g0251 others(31): Show |
34 | HG00408.hp1 HG00438.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.2594+938_2594+941d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTT | 17 | a0001c0001t0019g0259 a0002c0002t0001g0354 a0002c0002t0001g0393 others(14): Show |
17 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2594+937_2594+941d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTT | 12 | a0001c0001t0003g0201 a0001c0001t0003g0249 a0001c0001t0003g0255 others(9): Show |
12 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2594+936_2594+941d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT | 9 | a0001c0001t0003g0258 a0001c0005t0003g0014 a0002c0002t0001g0362 others(6): Show |
9 | HG00738.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2594+935_2594+941d others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0005t0003g0015 others(8): Show |
11 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.2594+934_2594+941d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0003g0210 a0001c0001t0019g0208 a0001c0001t0023g0209 others(4): Show |
7 | HG01123.hp1 HG02615.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594+933_2594+941d others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0003g0206 a0001c0005t0003g0010 |
2 | HG02273.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2594+932_2594+941d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0003g0214 a0003c0004t0007g0329 a0003c0004t0007g0340 |
3 | HG00099.hp2 HG00438.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2594+931_2594+941d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0027g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2594+930_2594+941d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(6): Show |
9 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0267 others(6): Show |
9 | HG02273.hp2 HG02559.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2594+929_2594+941d others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0003g0263 a0001c0001t0003g0266 a0003c0004t0007g0336 |
3 | HG03710.hp1 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2594+928_2594+941d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(8): Show |
2 | a0001c0005t0003g0008 a0005c0011t0007g0338 |
2 | HG03540.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2594+927_2594+941d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0207 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2594+926_2594+941d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0003g0213 a0003c0004t0044g0319 |
2 | HG02886.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2594+925_2594+941d others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(12): Show |
2 | a0001c0005t0003g0007 a0001c0005t0003g0012 |
2 | HG01978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2594+923_2594+941d others(21): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2594+922_2594+941d others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(19): Show |
1 | a0003c0004t0031g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2594+916_2594+941d others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0203 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2594+912_2594+941d others(32): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTT | C | 11 | a0001c0001t0009g0107 a0001c0001t0012g0028 a0001c0001t0012g0178 others(8): Show |
11 | HG00609.hp2 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2594+938_2594+941d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTT | C | 21 | a0001c0001t0009g0102 a0001c0001t0009g0105 a0001c0001t0009g0106 others(18): Show |
21 | HG01243.hp2 HG02132.hp2 HG02809.hp2 others(18): Show |
intron_variant | MODIFIER | c.2594+937_2594+941d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT | C | 15 | a0001c0001t0002g0034 a0001c0001t0003g0261 a0001c0001t0004g0196 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.2594+935_2594+941d others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(1): Show |
C | 51 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0004g0082 others(48): Show |
51 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.2594+934_2594+941d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(2): Show |
C | 24 | a0001c0001t0004g0236 a0001c0001t0006g0078 a0001c0001t0006g0080 others(21): Show |
24 | HG00544.hp1 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2594+933_2594+941d others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0003g0212 a0001c0001t0039g0033 a0002c0002t0001g0404 others(2): Show |
5 | HG02071.hp2 HG03209.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+932_2594+941d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0076g0083 a0001c0009t0017g0002 a0001c0009t0017g0302 others(3): Show |
7 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2594+931_2594+941d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0012g0115 a0002c0002t0001g0384 a0002c0002t0001g0392 others(3): Show |
6 | HG02630.hp2 NA18940.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594+930_2594+941d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0014g0233 a0001c0006t0030g0292 a0003c0004t0062g0335 |
3 | HG02572.hp1 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2594+929_2594+941d others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(7): Show |
C | 17 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(14): Show |
17 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2594+928_2594+941d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0034g0173 a0001c0006t0041g0286 a0001c0006t0041g0287 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2594+927_2594+941d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0004g0274 a0002c0002t0001g0414 |
2 | HG00735.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2594+926_2594+941d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(10): Show |
C | 39 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(36): Show |
39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2594+925_2594+941d others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0190 a0001c0001t0015g0191 |
2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2594+921_2594+941d others(23): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032365 | CTTTTTTT others(15): Show |
C | 1 | a0001c0007t0050g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2594+920_2594+941d others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | |||||||
chr9:109032374 | T | TCC | 3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0003c0004t0002g0321 |
3 | HG03491.hp1 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2594+932_2594+933i others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032374 | |||||||
chr9:109032383 | T | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+924A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032383 | |||||||
chr9:109032451 | C | T | 1 | a0002c0002t0001g0383 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2594+856G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032451 | |||||||
chr9:109032544 | C | T | 1 | a0003c0004t0044g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2594+763G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032544 | |||||||
chr9:109032737 | G | A | 2 | a0001c0001t0004g0216 a0001c0001t0004g0221 |
2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2594+570C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032737 | |||||||
chr9:109032807 | C | CT | 56 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(53): Show |
57 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2594+499dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | |||||||
chr9:109032807 | CT | C | 42 | a0001c0001t0003g0255 a0001c0001t0005g0101 a0001c0001t0005g0121 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.2594+499delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | |||||||
chr9:109032807 | CTT | C | 71 | a0001c0001t0020g0126 a0001c0001t0020g0279 a0001c0001t0043g0127 others(68): Show |
71 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.2594+498_2594+499d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | |||||||
chr9:109032827 | T | A | 1 | a0001c0001t0075g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2594+480A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032827 | |||||||
chr9:109032827 | TA | T | 7 | a0001c0001t0006g0096 a0001c0001t0022g0003 a0001c0009t0017g0002 others(4): Show |
8 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.2594+479delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032827 | |||||||
chr9:109032828 | A | T | 56 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.2594+479T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032828 | |||||||
chr9:109033053 | T | C | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+254A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033053 | |||||||
chr9:109033078 | C | T | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2594+229G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033078 | |||||||
chr9:109033092 | C | T | 1 | a0003c0004t0007g0343 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2594+215G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033092 | |||||||
chr9:109033194 | T | C | 1 | a0001c0007t0004g0297 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2594+113A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033194 | |||||||
chr9:109033221 | A | G | 3 | a0003c0004t0042g0314 a0003c0004t0042g0334 a0003c0004t0062g0335 |
3 | HG02630.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2594+86T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033221 | |||||||
chr9:109033281 | C | T | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+26G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033281 | |||||||
chr9:109033285 | T | C | 29 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2594+22A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033285 | |||||||
chr9:109033658 | TAATATTG others(9): Show |
T | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2400-173_2400-158d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033658 | |||||||
chr9:109033913 | T | C | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2400-412A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033913 | |||||||
chr9:109033951 | T | C | 75 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2400-450A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033951 | |||||||
chr9:109034137 | T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2400-636A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034137 | |||||||
chr9:109034236 | A | G | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-735T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034236 | |||||||
chr9:109034314 | G | C | 3 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 |
3 | HG01261.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2400-813C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034314 | |||||||
chr9:109034427 | A | C | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2400-926T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034427 | |||||||
chr9:109034473 | A | T | 141 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2400-972T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034473 | |||||||
chr9:109034477 | C | T | 1 | a0001c0005t0023g0013 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2400-976G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034477 | |||||||
chr9:109034561 | C | T | 6 | a0001c0001t0009g0106 a0001c0001t0009g0108 a0001c0001t0009g0111 others(3): Show |
6 | HG02132.hp2 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-1060G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034561 | |||||||
chr9:109034589 | G | A | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2400-1088C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034589 | |||||||
chr9:109034610 | C | T | 35 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(32): Show |
35 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.2400-1109G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034610 | |||||||
chr9:109034619 | A | AT | 8 | a0001c0001t0005g0133 a0001c0001t0005g0145 a0001c0001t0005g0146 others(5): Show |
8 | HG01081.hp1 HG01257.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1119dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034619 | |||||||
chr9:109034619 | A | C | 27 | a0001c0001t0009g0077 a0001c0001t0009g0102 a0001c0001t0009g0105 others(24): Show |
27 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.2400-1118T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034619 | |||||||
chr9:109034684 | G | A | 1 | a0001c0001t0039g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2400-1183C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034684 | |||||||
chr9:109034697 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2400-1196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034697 | |||||||
chr9:109034721 | C | T | 30 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(27): Show |
30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2400-1220G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034721 | |||||||
chr9:109034932 | G | A | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2399+1274C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034932 | |||||||
chr9:109034993 | G | C | 2 | a0001c0001t0013g0229 a0001c0001t0013g0230 |
2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2399+1213C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034993 | |||||||
chr9:109035014 | G | A | 3 | a0001c0001t0076g0083 a0003c0012t0063g0022 a0003c0018t0066g0307 |
3 | HG02055.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2399+1192C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035014 | |||||||
chr9:109035106 | G | A | 1 | a0001c0001t0045g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2399+1100C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035106 | |||||||
chr9:109035123 | C | T | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2399+1083G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035123 | |||||||
chr9:109035156 | C | CA | 81 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0220 others(78): Show |
81 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2399+1049dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | |||||||
chr9:109035156 | CA | C | 18 | a0001c0001t0004g0221 a0001c0001t0008g0162 a0001c0001t0008g0163 others(15): Show |
19 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.2399+1049delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | |||||||
chr9:109035156 | CAA | C | 23 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2399+1048_2399+104 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | |||||||
chr9:109035415 | T | C | 8 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0207 others(5): Show |
8 | HG02273.hp1 NA18940.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2399+791A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035415 | |||||||
chr9:109035737 | C | T | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2399+469G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035737 | |||||||
chr9:109035776 | T | C | 32 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(29): Show |
32 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.2399+430A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035776 | |||||||
chr9:109035819 | T | C | 1 | a0001c0001t0046g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2399+387A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035819 | |||||||
chr9:109035878 | G | C | 52 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(49): Show |
52 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.2399+328C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035878 | |||||||
chr9:109035879 | G | A | 1 | a0001c0001t0011g0189 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2399+327C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035879 | |||||||
chr9:109035913 | G | A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2399+293C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035913 | |||||||
chr9:109035940 | CA | C | 158 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(155): Show |
159 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.2399+265delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | |||||||
chr9:109035940 | CAA | C | 179 | a0001c0001t0002g0051 a0001c0001t0005g0101 a0001c0001t0005g0121 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2399+264_2399+265d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | |||||||
chr9:109035940 | CAAA | C | 6 | a0001c0001t0011g0278 a0002c0002t0001g0368 a0002c0002t0001g0403 others(3): Show |
6 | HG01517.hp1 HG02165.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2399+263_2399+265d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | |||||||
chr9:109035991 | CA | C | 354 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(351): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2399+214delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035991 | |||||||
chr9:109036008 | A | C | 53 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(50): Show |
53 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2399+198T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036008 | |||||||
chr9:109036045 | C | A | 176 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.2399+161G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036045 | |||||||
chr9:109036059 | T | C | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2399+147A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036059 | |||||||
chr9:109036081 | T | C | 1 | a0001c0001t0020g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2399+125A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036081 | |||||||
chr9:109036088 | G | A | 1 | a0003c0004t0083g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2399+118C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036088 | |||||||
chr9:109036135 | T | C | 32 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(29): Show |
32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2399+71A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036135 | |||||||
chr9:109036143 | T | TA | 36 | a0001c0001t0006g0089 a0001c0001t0007g0030 a0001c0001t0065g0029 others(33): Show |
37 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.2399+62dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | |||||||
chr9:109036143 | T | TAAAAAAA others(304): Show |
1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2399+62_2399+63ins others(311): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | |||||||
chr9:109036143 | TA | T | 97 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(94): Show |
97 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2399+62delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | |||||||
chr9:109036471 | C | T | 370 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(367): Show |
371 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.2225-91G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109036471 | |||||||
chr9:109036818 | G | A | 20 | a0001c0001t0009g0102 a0001c0001t0009g0106 a0001c0001t0009g0107 others(17): Show |
20 | HG00609.hp2 HG02132.hp2 HG04204.hp2 others(17): Show |
intron_variant | MODIFIER | c.2225-438C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109036818 | |||||||
chr9:109037072 | C | T | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2225-692G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037072 | |||||||
chr9:109037089 | G | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(51): Show |
55 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2225-709C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037089 | |||||||
chr9:109037283 | A | C | 404 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(401): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.2224+734T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037283 | |||||||
chr9:109037433 | G | T | 1 | a0004c0003t0002g0063 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2224+584C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037433 | |||||||
chr9:109037442 | T | A | 1 | a0004c0003t0002g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2224+575A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037442 | |||||||
chr9:109037459 | G | A | 2 | a0002c0002t0010g0399 a0002c0002t0078g0353 |
2 | NA18971.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2224+558C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037459 | |||||||
chr9:109037610 | T | C | 2 | a0003c0004t0017g0324 a0003c0004t0017g0325 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2224+407A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037610 | |||||||
chr9:109037916 | T | C | 15 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0035 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.2224+101A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037916 | |||||||
chr9:109037945 | T | C | 29 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.2224+72A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037945 | |||||||
chr9:109037954 | G | A | 284 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(281): Show |
285 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2224+63C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037954 | |||||||
chr9:109037987 | G | A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2224+30C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037987 | |||||||
chr9:109038338 | AAT | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2124-223_2124-222d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038338 | |||||||
chr9:109038359 | A | T | 2 | a0002c0002t0001g0370 a0002c0002t0001g0377 |
2 | HG02027.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2124-242T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038359 | |||||||
chr9:109038427 | C | T | 3 | a0001c0001t0027g0199 a0001c0001t0027g0211 a0001c0001t0027g0260 |
3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2124-310G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038427 | |||||||
chr9:109038471 | A | T | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2124-354T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038471 | |||||||
chr9:109038478 | G | A | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-361C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038478 | |||||||
chr9:109038599 | G | T | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-482C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038599 | |||||||
chr9:109038683 | T | C | 1 | a0003c0008t0016g0309 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2124-566A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038683 | |||||||
chr9:109038687 | T | A | 1 | a0001c0001t0006g0095 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2124-570A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038687 | |||||||
chr9:109038876 | A | G | 3 | a0002c0002t0001g0359 a0002c0002t0047g0358 a0002c0002t0047g0360 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2124-759T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038876 | |||||||
chr9:109038963 | T | C | 1 | a0002c0002t0010g0389 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2124-846A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038963 | |||||||
chr9:109039005 | T | C | 404 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(401): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.2124-888A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039005 | |||||||
chr9:109039032 | T | C | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-915A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039032 | |||||||
chr9:109039045 | G | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-928C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039045 | |||||||
chr9:109039064 | G | A | 42 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0004g0182 others(39): Show |
42 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2124-947C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039064 | |||||||
chr9:109039073 | T | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-956A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039073 | |||||||
chr9:109039181 | G | A | 29 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(26): Show |
29 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.2124-1064C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039181 | |||||||
chr9:109039335 | G | A | 1 | a0003c0018t0066g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2124-1218C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039335 | |||||||
chr9:109039388 | C | A | 1 | a0001c0001t0028g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2124-1271G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039388 | |||||||
chr9:109039415 | C | T | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2124-1298G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039415 | |||||||
chr9:109039444 | G | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-1327C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039444 | |||||||
chr9:109039469 | G | A | 1 | a0003c0012t0063g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2124-1352C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039469 | |||||||
chr9:109039470 | C | A | 1 | a0003c0012t0063g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2124-1353G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039470 | |||||||
chr9:109039612 | C | T | 2 | a0002c0002t0001g0393 a0002c0002t0001g0395 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2124-1495G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039612 | |||||||
chr9:109039820 | G | A | 1 | a0002c0002t0001g0363 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2124-1703C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039820 | |||||||
chr9:109039836 | G | A | 2 | a0001c0001t0035g0271 a0001c0001t0035g0272 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2124-1719C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039836 | |||||||
chr9:109039866 | T | C | 8 | a0001c0001t0014g0183 a0001c0001t0014g0187 a0001c0001t0014g0233 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2124-1749A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039866 | |||||||
chr9:109039966 | T | G | 39 | a0001c0001t0005g0101 a0001c0001t0005g0121 a0001c0001t0005g0123 others(36): Show |
39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2124-1849A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039966 | |||||||
chr9:109040049 | C | T | 3 | a0001c0001t0014g0234 a0001c0001t0025g0198 a0003c0004t0081g0342 |
3 | HG02809.hp1 HG03516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2124-1932G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040049 | |||||||
chr9:109040334 | T | A | 75 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2124-2217A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040334 | |||||||
chr9:109040385 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2124-2268G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040385 | |||||||
chr9:109040451 | T | C | 65 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(62): Show |
65 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2124-2334A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040451 | |||||||
chr9:109040603 | A | G | 2 | a0001c0001t0009g0107 a0001c0001t0059g0109 |
2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2124-2486T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040603 | |||||||
chr9:109040802 | A | G | 1 | a0001c0001t0045g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2124-2685T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040802 | |||||||
chr9:109040848 | G | T | 73 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(70): Show |
73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2124-2731C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040848 | |||||||
chr9:109040942 | G | A | 1 | a0001c0001t0005g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2124-2825C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040942 | |||||||
chr9:109040979 | C | T | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-2862G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040979 | |||||||
chr9:109041029 | G | A | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-2912C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041029 | |||||||
chr9:109041222 | T | G | 5 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0265 others(2): Show |
5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.2124-3105A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041222 | |||||||
chr9:109041270 | G | A | 4 | a0002c0002t0001g0384 a0002c0002t0001g0385 a0002c0002t0001g0392 others(1): Show |
4 | NA18973.hp2 NA18974.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2124-3153C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041270 | |||||||
chr9:109041342 | T | C | 1 | a0002c0002t0001g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2124-3225A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041342 | |||||||
chr9:109041381 | C | G | 7 | a0001c0007t0004g0297 a0001c0007t0004g0298 a0001c0007t0004g0299 others(4): Show |
7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-3264G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041381 | |||||||
chr9:109041428 | G | A | 32 | a0001c0001t0005g0101 a0001c0001t0011g0189 a0001c0001t0011g0275 others(29): Show |
32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2124-3311C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041428 | |||||||
chr9:109041453 | A | AT | 112 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(109): Show |
114 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2124-3337dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | A | ATT | 24 | a0001c0001t0004g0274 a0001c0001t0007g0030 a0001c0001t0008g0161 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2124-3338_2124-333 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | A | ATTT | 8 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0005g0101 others(5): Show |
8 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2124-3339_2124-333 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | AT | A | 70 | a0001c0001t0005g0121 a0001c0001t0005g0125 a0001c0001t0005g0129 others(67): Show |
70 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2124-3337delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | ATT | A | 8 | a0001c0001t0005g0123 a0001c0001t0005g0144 a0001c0001t0005g0152 others(5): Show |
8 | HG00733.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2124-3338_2124-333 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | ATTT | A | 7 | a0001c0001t0009g0112 a0003c0008t0016g0304 a0003c0008t0016g0305 others(4): Show |
7 | HG02132.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124-3339_2124-333 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041453 | ATTTTTTT | A | 8 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(5): Show |
8 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2124-3343_2124-333 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | |||||||
chr9:109041531 | TTGGCTCA others(1375): Show |
T | 3 | a0001c0001t0034g0173 a0001c0001t0035g0271 a0001c0001t0035g0272 |
3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2124-4796_2124-341 others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041531 | |||||||
chr9:109041595 | T | C | 7 | a0001c0007t0004g0297 a0001c0007t0004g0298 a0001c0007t0004g0299 others(4): Show |
7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-3478A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041595 | |||||||
chr9:109041959 | G | A | 73 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(70): Show |
73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2124-3842C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041959 | |||||||
chr9:109042024 | A | T | 2 | a0001c0001t0011g0189 a0001c0001t0046g0188 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2124-3907T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042024 | |||||||
chr9:109042153 | C | T | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2124-4036G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042153 | |||||||
chr9:109042238 | T | C | 30 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(27): Show |
30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2124-4121A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042238 | |||||||
chr9:109042781 | A | G | 1 | a0001c0001t0008g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2124-4664T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042781 | |||||||
chr9:109042833 | C | T | 34 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(31): Show |
35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-4716G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042833 | |||||||
chr9:109042839 | A | AT | 78 | a0001c0001t0003g0232 a0001c0001t0003g0250 a0001c0001t0003g0251 others(75): Show |
78 | HG00609.hp2 HG01109.hp2 HG01243.hp2 others(75): Show |
intron_variant | MODIFIER | c.2124-4723dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | |||||||
chr9:109042839 | A | ATT | 34 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(31): Show |
34 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2124-4724_2124-472 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | |||||||
chr9:109042839 | AT | A | 10 | a0001c0001t0002g0047 a0001c0001t0005g0136 a0001c0001t0005g0141 others(7): Show |
10 | HG01070.hp2 HG01516.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.2124-4723delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | |||||||
chr9:109042839 | ATTTTTTT others(3): Show |
A | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2124-4732_2124-472 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | |||||||
chr9:109042885 | G | A | 1 | a0001c0001t0005g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2124-4768C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042885 | |||||||
chr9:109042908 | C | T | 53 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(50): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2124-4791G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042908 | |||||||
chr9:109043133 | T | C | 1 | a0001c0001t0014g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2124-5016A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043133 | |||||||
chr9:109043206 | A | G | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2124-5089T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043206 | |||||||
chr9:109043281 | G | T | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2124-5164C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043281 | |||||||
chr9:109043284 | G | A | 1 | a0001c0001t0004g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2124-5167C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043284 | |||||||
chr9:109043585 | T | C | 7 | a0001c0007t0004g0297 a0001c0007t0004g0298 a0001c0007t0004g0299 others(4): Show |
7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-5468A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043585 | |||||||
chr9:109043611 | A | AATTCACA others(1): Show |
404 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(401): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.2124-5495_2124-549 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043611 | |||||||
chr9:109043809 | T | C | 380 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(377): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.2124-5692A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043809 | |||||||
chr9:109043975 | G | A | 7 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(4): Show |
7 | NA18948.hp2 NA18952.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124-5858C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043975 | |||||||
chr9:109043995 | A | C | 24 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(21): Show |
24 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2124-5878T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043995 | |||||||
chr9:109044127 | C | T | 1 | a0004c0003t0002g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2124-6010G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044127 | |||||||
chr9:109044250 | G | A | 10 | a0004c0003t0002g0040 a0004c0003t0002g0060 a0004c0003t0002g0065 others(7): Show |
10 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.2123+6033C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044250 | |||||||
chr9:109044479 | C | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2123+5804G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044479 | |||||||
chr9:109044583 | G | C | 36 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(33): Show |
36 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2123+5700C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044583 | |||||||
chr9:109044671 | G | A | 1 | a0002c0002t0001g0363 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2123+5612C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044671 | |||||||
chr9:109044710 | A | C | 8 | a0001c0001t0014g0183 a0001c0001t0014g0187 a0001c0001t0014g0233 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2123+5573T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044710 | |||||||
chr9:109044762 | G | GT | 52 | a0001c0001t0002g0190 a0001c0001t0003g0210 a0001c0001t0003g0263 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.2123+5520dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044762 | |||||||
chr9:109044762 | GT | G | 33 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(30): Show |
33 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.2123+5520delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044762 | |||||||
chr9:109044789 | TCTCA | T | 12 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2123+5490_2123+549 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044789 | |||||||
chr9:109044885 | G | T | 1 | a0001c0001t0012g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2123+5398C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044885 | |||||||
chr9:109044892 | T | C | 4 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 others(1): Show |
4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2123+5391A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044892 | |||||||
chr9:109044993 | C | T | 384 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(381): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.2123+5290G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044993 | |||||||
chr9:109045040 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2123+5243C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045040 | |||||||
chr9:109045045 | C | A | 1 | a0002c0002t0001g0388 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2123+5238G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045045 | |||||||
chr9:109045066 | C | A | 31 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0084 others(28): Show |
31 | HG00544.hp1 HG00558.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2123+5217G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045066 | |||||||
chr9:109045114 | A | G | 236 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(233): Show |
237 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.2123+5169T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045114 | |||||||
chr9:109045534 | G | C | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2123+4749C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045534 | |||||||
chr9:109045576 | A | T | 24 | a0001c0001t0004g0193 a0001c0001t0004g0218 a0001c0001t0009g0102 others(21): Show |
24 | HG00609.hp2 HG02132.hp1 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.2123+4707T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045576 | |||||||
chr9:109045840 | A | C | 1 | a0003c0004t0031g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2123+4443T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045840 | |||||||
chr9:109045872 | G | C | 236 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(233): Show |
237 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.2123+4411C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045872 | |||||||
chr9:109046085 | C | T | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2123+4198G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046085 | |||||||
chr9:109046086 | G | A | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2123+4197C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046086 | |||||||
chr9:109046152 | C | G | 54 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(51): Show |
54 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2123+4131G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046152 | |||||||
chr9:109046157 | C | A | 54 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(51): Show |
54 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2123+4126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046157 | |||||||
chr9:109046622 | A | G | 1 | a0002c0002t0018g0352 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2123+3661T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046622 | |||||||
chr9:109047015 | A | C | 77 | a0001c0001t0003g0250 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2123+3268T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047015 | |||||||
chr9:109047038 | A | G | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2123+3245T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047038 | |||||||
chr9:109047250 | A | G | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.2123+3033T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047250 | |||||||
chr9:109047312 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0017g0324 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2123+2971C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047312 | |||||||
chr9:109047840 | T | C | 2 | a0003c0012t0063g0022 a0003c0018t0066g0307 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2123+2443A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047840 | |||||||
chr9:109047887 | G | A | 1 | a0001c0001t0014g0248 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2123+2396C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047887 | |||||||
chr9:109047943 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2123+2340C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047943 | |||||||
chr9:109048109 | A | G | 2 | a0003c0004t0007g0326 a0003c0004t0007g0330 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2123+2174T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048109 | |||||||
chr9:109048150 | G | A | 1 | a0001c0001t0008g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2123+2133C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048150 | |||||||
chr9:109048293 | C | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(49): Show |
53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2123+1990G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048293 | |||||||
chr9:109048478 | A | C | 1 | a0002c0002t0018g0356 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2123+1805T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048478 | |||||||
chr9:109048524 | T | C | 405 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(402): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2123+1759A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048524 | |||||||
chr9:109048525 | G | A | 114 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(111): Show |
114 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2123+1758C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048525 | |||||||
chr9:109048563 | G | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 |
3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2123+1720C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048563 | |||||||
chr9:109048612 | C | T | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2123+1671G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048612 | |||||||
chr9:109048619 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2123+1664T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048619 | |||||||
chr9:109048837 | G | C | 1 | a0001c0001t0012g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2123+1446C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048837 | |||||||
chr9:109048847 | A | T | 1 | a0001c0001t0013g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2123+1436T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048847 | |||||||
chr9:109048880 | G | T | 1 | a0003c0004t0083g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2123+1403C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048880 | |||||||
chr9:109048929 | G | T | 1 | a0001c0001t0073g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2123+1354C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048929 | |||||||
chr9:109048987 | G | C | 1 | a0001c0001t0009g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2123+1296C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048987 | |||||||
chr9:109049189 | G | T | 1 | a0003c0004t0007g0330 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2123+1094C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049189 | |||||||
chr9:109049414 | T | C | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2123+869A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049414 | |||||||
chr9:109049506 | G | A | 56 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(53): Show |
56 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2123+777C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049506 | |||||||
chr9:109049593 | G | A | 4 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2123+690C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049593 | |||||||
chr9:109049636 | G | C | 1 | a0002c0002t0021g0386 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2123+647C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049636 | |||||||
chr9:109049848 | G | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 |
3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2123+435C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049848 | |||||||
chr9:109049906 | C | T | 2 | a0001c0001t0004g0196 a0001c0007t0004g0294 |
2 | HG02148.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2123+377G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049906 | |||||||
chr9:109049980 | C | T | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2123+303G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049980 | |||||||
chr9:109049994 | G | A | 1 | a0001c0006t0011g0282 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2123+289C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049994 | |||||||
chr9:109050039 | G | A | 2 | a0001c0001t0005g0121 a0001c0001t0043g0122 |
2 | NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2123+244C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050039 | |||||||
chr9:109050149 | T | C | 2 | a0001c0001t0003g0201 a0001c0001t0003g0249 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2123+134A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050149 | |||||||
chr9:109050175 | A | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2123+108T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050175 | |||||||
chr9:109050545 | C | T | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1977+25G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 13/17 | chr9 | 109050545 | |||||||
chr9:109050740 | A | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-48T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050740 | |||||||
chr9:109050743 | T | A | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1855-51A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050743 | |||||||
chr9:109050831 | T | TA | 52 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(49): Show |
52 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1855-140dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050831 | |||||||
chr9:109050843 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1855-151C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050843 | |||||||
chr9:109050928 | A | G | 1 | a0001c0001t0020g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1855-236T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050928 | |||||||
chr9:109050933 | T | G | 1 | a0001c0001t0065g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1855-241A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050933 | |||||||
chr9:109051054 | G | C | 1 | a0003c0004t0007g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1855-362C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051054 | |||||||
chr9:109051129 | A | G | 2 | a0001c0001t0033g0159 a0001c0001t0033g0165 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1855-437T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051129 | |||||||
chr9:109051241 | G | A | 2 | a0001c0001t0003g0201 a0001c0001t0003g0249 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1855-549C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051241 | |||||||
chr9:109051295 | A | AAC | 48 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0225 others(45): Show |
48 | HG00408.hp2 HG00609.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1855-605_1855-604d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACAC | 85 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0039 others(82): Show |
85 | HG00609.hp2 HG00621.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.1855-607_1855-604d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACAC | 30 | a0001c0001t0007g0030 a0001c0001t0009g0108 a0001c0001t0009g0111 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.1855-609_1855-604d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(1): Show |
26 | a0001c0001t0002g0001 a0001c0001t0002g0045 a0001c0001t0002g0046 others(23): Show |
27 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1855-611_1855-604d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(3): Show |
6 | a0003c0004t0007g0336 a0003c0004t0007g0337 a0003c0008t0067g0306 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855-613_1855-604d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(5): Show |
2 | a0003c0004t0031g0331 a0003c0004t0083g0332 |
2 | HG02615.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1855-615_1855-604d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(7): Show |
2 | a0001c0001t0039g0033 a0003c0008t0016g0308 |
2 | HG00733.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1855-617_1855-604d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(9): Show |
1 | a0004c0003t0015g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1855-619_1855-604d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | A | AACACACA others(13): Show |
1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-623_1855-604d others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | AAC | A | 104 | a0001c0001t0003g0202 a0001c0001t0003g0203 a0001c0001t0003g0204 others(101): Show |
104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1855-605_1855-604d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | AACAC | A | 14 | a0001c0001t0003g0214 a0001c0001t0006g0088 a0001c0001t0006g0089 others(11): Show |
14 | HG00438.hp2 HG04228.hp1 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.1855-607_1855-604d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | AACACAC | A | 5 | a0001c0001t0003g0256 a0001c0001t0022g0003 a0001c0001t0022g0004 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1855-609_1855-604d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051295 | AACACACA others(11): Show |
A | 1 | a0001c0001t0073g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1855-621_1855-604d others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | |||||||
chr9:109051363 | C | T | 4 | a0001c0001t0006g0078 a0001c0001t0006g0095 a0001c0001t0006g0099 others(1): Show |
4 | NA18961.hp2 NA18998.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855-671G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051363 | |||||||
chr9:109051380 | T | C | 1 | a0001c0001t0006g0084 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1855-688A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051380 | |||||||
chr9:109051438 | T | C | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1855-746A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051438 | |||||||
chr9:109051521 | C | A | 5 | a0001c0001t0008g0160 a0001c0001t0008g0162 a0001c0001t0008g0163 others(2): Show |
5 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855-829G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051521 | |||||||
chr9:109051551 | C | T | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1855-859G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051551 | |||||||
chr9:109051552 | G | A | 108 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(105): Show |
109 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1855-860C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051552 | |||||||
chr9:109051921 | G | C | 2 | a0001c0001t0038g0169 a0001c0001t0038g0172 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1855-1229C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051921 | |||||||
chr9:109052055 | T | C | 1 | a0001c0006t0060g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1855-1363A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052055 | |||||||
chr9:109052133 | TTATTA | T | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1855-1446_1855-144 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052133 | |||||||
chr9:109052198 | A | G | 111 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(108): Show |
112 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.1855-1506T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052198 | |||||||
chr9:109052218 | C | T | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1855-1526G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052218 | |||||||
chr9:109052387 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1855-1695G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052387 | |||||||
chr9:109052439 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-1747A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052439 | |||||||
chr9:109052476 | A | G | 114 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(111): Show |
114 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1855-1784T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052476 | |||||||
chr9:109052531 | T | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1855-1839A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052531 | |||||||
chr9:109052673 | A | G | 2 | a0001c0001t0014g0234 a0001c0001t0025g0198 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1855-1981T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052673 | |||||||
chr9:109052795 | T | C | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1855-2103A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052795 | |||||||
chr9:109052823 | A | T | 1 | a0001c0005t0003g0014 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1855-2131T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052823 | |||||||
chr9:109052834 | G | C | 2 | a0001c0001t0008g0162 a0001c0001t0008g0163 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1855-2142C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052834 | |||||||
chr9:109052852 | A | G | 2 | a0001c0001t0014g0248 a0001c0001t0025g0262 |
2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1855-2160T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052852 | |||||||
chr9:109052888 | C | A | 8 | a0001c0001t0011g0189 a0001c0001t0046g0188 a0001c0006t0011g0280 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1855-2196G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052888 | |||||||
chr9:109052918 | CA | C | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1855-2227delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052918 | |||||||
chr9:109053060 | C | A | 135 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1855-2368G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053060 | |||||||
chr9:109053080 | T | G | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1855-2388A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053080 | |||||||
chr9:109053200 | C | T | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1855-2508G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053200 | |||||||
chr9:109053209 | T | C | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-2517A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053209 | |||||||
chr9:109053376 | G | A | 1 | a0001c0001t0004g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1855-2684C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053376 | |||||||
chr9:109053413 | C | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-2721G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053413 | |||||||
chr9:109053414 | G | A | 99 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(96): Show |
99 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1855-2722C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053414 | |||||||
chr9:109053618 | G | C | 1 | a0001c0001t0023g0209 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1855-2926C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053618 | |||||||
chr9:109053637 | G | C | 99 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(96): Show |
99 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1855-2945C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053637 | |||||||
chr9:109053703 | T | C | 1 | a0002c0002t0001g0375 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1855-3011A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053703 | |||||||
chr9:109054040 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1854+3151T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054040 | |||||||
chr9:109054099 | G | A | 2 | a0002c0002t0001g0397 a0002c0002t0001g0398 |
2 | NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1854+3092C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054099 | |||||||
chr9:109054233 | A | G | 1 | a0002c0002t0001g0354 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1854+2958T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054233 | |||||||
chr9:109054328 | C | T | 1 | a0003c0004t0007g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1854+2863G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054328 | |||||||
chr9:109054401 | C | T | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+2790G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054401 | |||||||
chr9:109054622 | C | CA | 4 | a0001c0001t0040g0031 a0001c0009t0017g0002 a0001c0009t0017g0302 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1854+2568dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054622 | |||||||
chr9:109054623 | A | T | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1854+2568T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054623 | |||||||
chr9:109054691 | G | A | 2 | a0002c0002t0001g0351 a0002c0002t0018g0350 |
2 | HG00621.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1854+2500C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054691 | |||||||
chr9:109054722 | T | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1854+2469A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054722 | |||||||
chr9:109055102 | T | C | 1 | a0004c0003t0002g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1854+2089A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055102 | |||||||
chr9:109055148 | T | A | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854+2043A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055148 | |||||||
chr9:109055165 | C | G | 1 | a0001c0005t0003g0016 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1854+2026G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055165 | |||||||
chr9:109055239 | C | T | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1854+1952G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055239 | |||||||
chr9:109055352 | G | GCTGA | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1854+1838_1854+183 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055352 | |||||||
chr9:109055477 | C | T | 1 | a0001c0005t0024g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1854+1714G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055477 | |||||||
chr9:109055545 | A | G | 3 | a0001c0001t0009g0077 a0001c0001t0057g0118 a0001c0001t0058g0119 |
3 | HG01891.hp2 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1854+1646T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055545 | |||||||
chr9:109055637 | CT | C | 31 | a0001c0001t0003g0249 a0001c0001t0007g0030 a0001c0001t0065g0029 others(28): Show |
31 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1854+1553delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055637 | |||||||
chr9:109055674 | AC | A | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854+1516delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055674 | |||||||
chr9:109055894 | A | C | 29 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1854+1297T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055894 | |||||||
chr9:109055929 | C | T | 53 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1854+1262G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055929 | |||||||
chr9:109056152 | G | A | 1 | a0001c0001t0019g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1854+1039C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056152 | |||||||
chr9:109056232 | C | T | 8 | a0001c0001t0011g0189 a0001c0001t0046g0188 a0001c0006t0011g0280 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1854+959G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056232 | |||||||
chr9:109056319 | T | G | 1 | a0001c0001t0014g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1854+872A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056319 | |||||||
chr9:109056321 | T | C | 403 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(400): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1854+870A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056321 | |||||||
chr9:109056440 | C | CA | 130 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0001t0002g0047 others(127): Show |
130 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.1854+750dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | |||||||
chr9:109056440 | C | CAA | 27 | a0001c0001t0005g0121 a0001c0001t0005g0129 a0001c0001t0005g0137 others(24): Show |
27 | HG00609.hp1 HG01109.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1854+749_1854+750d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | |||||||
chr9:109056440 | C | CAAA | 29 | a0001c0001t0004g0238 a0001c0001t0005g0123 a0001c0001t0009g0108 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1854+748_1854+750d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | |||||||
chr9:109056440 | CA | C | 43 | a0001c0001t0006g0080 a0001c0001t0006g0084 a0001c0001t0006g0085 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1854+750delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | |||||||
chr9:109056440 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0008g0166 a0001c0001t0008g0167 a0001c0001t0008g0168 others(2): Show |
5 | HG02965.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1854+740_1854+750d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | |||||||
chr9:109056476 | T | A | 1 | a0001c0001t0004g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1854+715A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056476 | |||||||
chr9:109056488 | T | C | 403 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(400): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1854+703A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056488 | |||||||
chr9:109056558 | G | T | 1 | a0001c0001t0006g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1854+633C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056558 | |||||||
chr9:109056594 | C | G | 1 | a0005c0011t0007g0338 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1854+597G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056594 | |||||||
chr9:109056635 | T | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1854+556A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056635 | |||||||
chr9:109057049 | AG | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 |
3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1854+141delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109057049 | |||||||
chr9:109057057 | T | C | 1 | a0002c0002t0001g0378 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1854+134A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109057057 | |||||||
chr9:109057480 | C | T | 1 | a0003c0004t0031g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1723-158G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057480 | |||||||
chr9:109057494 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1723-172A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057494 | |||||||
chr9:109057518 | C | T | 36 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(33): Show |
36 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1723-196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057518 | |||||||
chr9:109057622 | G | A | 29 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1723-300C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057622 | |||||||
chr9:109057656 | C | G | 28 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1723-334G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057656 | |||||||
chr9:109057694 | T | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-372A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057694 | |||||||
chr9:109057775 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(48): Show |
52 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1723-453C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057775 | |||||||
chr9:109057920 | ACTTT | A | 33 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(30): Show |
33 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1723-602_1723-599d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057920 | |||||||
chr9:109057925 | C | CT | 101 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(98): Show |
101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1723-604dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057925 | |||||||
chr9:109057925 | CT | C | 14 | a0001c0001t0006g0084 a0001c0001t0006g0098 a0001c0001t0011g0278 others(11): Show |
14 | HG01099.hp2 HG02735.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1723-604delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057925 | |||||||
chr9:109057982 | C | T | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1723-660G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057982 | |||||||
chr9:109058005 | A | AT | 75 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(72): Show |
75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1723-684dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058005 | |||||||
chr9:109058018 | T | G | 4 | a0001c0001t0005g0101 a0001c0001t0076g0083 a0004c0003t0002g0063 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-696A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058018 | |||||||
chr9:109058020 | G | A | 138 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1723-698C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058020 | |||||||
chr9:109058086 | C | T | 1 | a0001c0001t0008g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1723-764G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058086 | |||||||
chr9:109058114 | C | A | 2 | a0001c0001t0014g0248 a0001c0001t0025g0262 |
2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-792G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058114 | |||||||
chr9:109058239 | C | T | 3 | a0001c0006t0041g0286 a0001c0006t0041g0287 a0001c0006t0061g0288 |
3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1723-917G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058239 | |||||||
chr9:109058296 | G | C | 1 | a0002c0002t0001g0390 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1723-974C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058296 | |||||||
chr9:109058328 | T | C | 53 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1723-1006A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058328 | |||||||
chr9:109058409 | T | C | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-1087A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058409 | |||||||
chr9:109058557 | T | C | 1 | a0001c0001t0009g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1723-1235A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058557 | |||||||
chr9:109058569 | A | T | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1723-1247T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058569 | |||||||
chr9:109058653 | G | T | 28 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1723-1331C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058653 | |||||||
chr9:109058670 | T | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-1348A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058670 | |||||||
chr9:109058872 | C | T | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1722+1482G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058872 | |||||||
chr9:109058934 | C | T | 1 | a0001c0001t0056g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1722+1420G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058934 | |||||||
chr9:109059175 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1722+1179C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059175 | |||||||
chr9:109059183 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1722+1171G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059183 | |||||||
chr9:109059185 | A | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1722+1169T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059185 | |||||||
chr9:109059191 | C | T | 8 | a0001c0001t0007g0030 a0003c0004t0007g0326 a0003c0004t0007g0329 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1722+1163G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059191 | |||||||
chr9:109059215 | T | G | 8 | a0001c0001t0011g0189 a0001c0001t0046g0188 a0001c0006t0011g0280 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1722+1139A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059215 | |||||||
chr9:109059250 | A | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1722+1104T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059250 | |||||||
chr9:109059641 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1722+713G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059641 | |||||||
chr9:109059662 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1722+692C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059662 | |||||||
chr9:109059672 | G | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1722+682C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059672 | |||||||
chr9:109059787 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1722+567A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059787 | |||||||
chr9:109059910 | GA | G | 29 | a0001c0001t0007g0030 a0001c0001t0009g0107 a0001c0001t0065g0029 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1722+443delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059910 | |||||||
chr9:109060039 | A | G | 1 | a0002c0002t0021g0386 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1722+315T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060039 | |||||||
chr9:109060054 | T | C | 1 | a0001c0001t0006g0094 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1722+300A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060054 | |||||||
chr9:109060123 | C | T | 4 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 others(1): Show |
4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1722+231G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060123 | |||||||
chr9:109060200 | T | G | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+154A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060200 | |||||||
chr9:109060218 | A | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1722+136T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060218 | |||||||
chr9:109060228 | T | C | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1722+126A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060228 | |||||||
chr9:109060586 | C | T | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-134G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060586 | |||||||
chr9:109060610 | G | A | 2 | a0001c0006t0046g0285 a0001c0006t0072g0284 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1624-158C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060610 | |||||||
chr9:109060754 | C | A | 3 | a0001c0006t0041g0286 a0001c0006t0041g0287 a0001c0006t0061g0288 |
3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1624-302G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060754 | |||||||
chr9:109060774 | G | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1624-322C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060774 | |||||||
chr9:109060803 | T | A | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1624-351A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060803 | |||||||
chr9:109060816 | A | T | 3 | a0002c0002t0001g0365 a0002c0002t0001g0397 a0002c0002t0001g0398 |
3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1624-364T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060816 | |||||||
chr9:109060838 | T | C | 1 | a0002c0002t0001g0357 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1624-386A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060838 | |||||||
chr9:109060848 | T | A | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1624-396A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060848 | |||||||
chr9:109060861 | T | C | 1 | a0001c0001t0005g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1624-409A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060861 | |||||||
chr9:109060884 | G | A | 173 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1624-432C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060884 | |||||||
chr9:109060897 | A | G | 1 | a0001c0001t0073g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1624-445T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060897 | |||||||
chr9:109060914 | T | C | 1 | a0001c0007t0004g0301 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1624-462A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060914 | |||||||
chr9:109061018 | C | T | 25 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1624-566G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061018 | |||||||
chr9:109061096 | G | A | 1 | a0003c0004t0007g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1624-644C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061096 | |||||||
chr9:109061225 | A | G | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1624-773T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061225 | |||||||
chr9:109061272 | C | T | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1624-820G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061272 | |||||||
chr9:109061418 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1624-966A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061418 | |||||||
chr9:109061630 | G | C | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1624-1178C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061630 | |||||||
chr9:109061668 | G | A | 3 | a0001c0001t0004g0182 a0001c0001t0036g0181 a0001c0006t0030g0290 |
3 | HG01261.hp1 NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1624-1216C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061668 | |||||||
chr9:109061669 | A | G | 3 | a0003c0004t0007g0336 a0003c0004t0031g0331 a0003c0004t0031g0333 |
3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1624-1217T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061669 | |||||||
chr9:109061691 | C | T | 4 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-1239G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061691 | |||||||
chr9:109061714 | G | A | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-1262C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061714 | |||||||
chr9:109061753 | G | A | 7 | a0002c0002t0010g0355 a0002c0002t0010g0379 a0002c0002t0010g0380 others(4): Show |
7 | HG01433.hp2 HG02004.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1301C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061753 | |||||||
chr9:109061760 | G | A | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-1308C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061760 | |||||||
chr9:109061935 | A | C | 1 | a0001c0001t0020g0131 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1624-1483T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061935 | |||||||
chr9:109061943 | G | A | 28 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1624-1491C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061943 | |||||||
chr9:109061970 | CATAA | C | 7 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(4): Show |
7 | HG01070.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1522_1624-151 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061970 | |||||||
chr9:109062347 | A | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1624-1895T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062347 | |||||||
chr9:109062453 | T | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-2001A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062453 | |||||||
chr9:109062549 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+1928G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062549 | |||||||
chr9:109062661 | T | A | 400 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(397): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.1623+1816A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062661 | |||||||
chr9:109062799 | C | T | 1 | a0001c0001t0015g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1623+1678G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062799 | |||||||
chr9:109062927 | G | A | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1623+1550C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062927 | |||||||
chr9:109062934 | C | T | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+1543G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062934 | |||||||
chr9:109062978 | G | GA | 28 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1623+1498dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062978 | |||||||
chr9:109062978 | GA | G | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1623+1498delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062978 | |||||||
chr9:109063076 | A | T | 31 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(28): Show |
31 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1623+1401T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063076 | |||||||
chr9:109063131 | C | CT | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623+1345dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063131 | |||||||
chr9:109063140 | G | A | 2 | a0005c0011t0007g0338 a0005c0011t0007g0339 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1623+1337C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063140 | |||||||
chr9:109063205 | TGCCTCCC others(25): Show |
T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+1240_1623+127 others(36): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063205 | |||||||
chr9:109063512 | A | G | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1623+965T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063512 | |||||||
chr9:109063521 | T | A | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1623+956A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063521 | |||||||
chr9:109063694 | A | G | 1 | a0001c0001t0045g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1623+783T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063694 | |||||||
chr9:109063752 | A | T | 55 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(52): Show |
56 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1623+725T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063752 | |||||||
chr9:109063767 | T | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+710A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063767 | |||||||
chr9:109063835 | C | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1623+642G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063835 | |||||||
chr9:109064128 | AC | A | 4 | a0001c0001t0004g0196 a0001c0001t0004g0241 a0001c0001t0004g0243 others(1): Show |
4 | HG01346.hp2 HG02148.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+348delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064128 | |||||||
chr9:109064190 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+287G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064190 | |||||||
chr9:109064259 | A | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+218T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064259 | |||||||
chr9:109064306 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1623+171G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064306 | |||||||
chr9:109064773 | G | A | 1 | a0001c0001t0065g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1533-206C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064773 | |||||||
chr9:109064773 | G | C | 1 | a0002c0002t0001g0388 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1533-206C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064773 | |||||||
chr9:109064928 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-361G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064928 | |||||||
chr9:109064941 | C | A | 1 | a0003c0004t0083g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1533-374G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064941 | |||||||
chr9:109064945 | G | A | 28 | a0001c0001t0011g0275 a0001c0001t0011g0277 a0001c0001t0011g0278 others(25): Show |
28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-378C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064945 | |||||||
chr9:109064974 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1533-407A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064974 | |||||||
chr9:109065298 | G | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-731C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065298 | |||||||
chr9:109065334 | G | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(54): Show |
59 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-767C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065334 | |||||||
chr9:109065397 | TG | T | 417 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(414): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.1533-831delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065397 | |||||||
chr9:109065447 | A | C | 3 | a0001c0001t0006g0084 a0001c0001t0006g0086 a0001c0001t0006g0087 |
3 | HG02027.hp2 HG02074.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1533-880T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065447 | |||||||
chr9:109065631 | T | C | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1533-1064A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065631 | |||||||
chr9:109065694 | G | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1533-1127C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065694 | |||||||
chr9:109065726 | C | T | 2 | a0002c0002t0001g0357 a0008c0019t0001g0406 |
2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1533-1159G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065726 | |||||||
chr9:109065743 | T | G | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-1176A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065743 | |||||||
chr9:109065758 | G | T | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1533-1191C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065758 | |||||||
chr9:109066315 | C | A | 2 | a0003c0004t0007g0340 a0003c0004t0071g0328 |
2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1533-1748G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066315 | |||||||
chr9:109066378 | C | T | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1533-1811G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066378 | |||||||
chr9:109066391 | G | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-1824C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066391 | |||||||
chr9:109066419 | C | T | 3 | a0001c0001t0009g0106 a0001c0001t0009g0108 a0001c0001t0009g0112 |
3 | HG02132.hp2 NA18977.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1533-1852G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066419 | |||||||
chr9:109066452 | C | CA | 95 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0042 others(92): Show |
96 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1533-1886dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAA | 35 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0039 others(32): Show |
35 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1533-1887_1533-188 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAA | 51 | a0001c0001t0004g0239 a0001c0001t0013g0230 a0001c0001t0027g0199 others(48): Show |
51 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1533-1888_1533-188 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAA | 18 | a0001c0001t0003g0266 a0001c0001t0004g0228 a0001c0001t0014g0233 others(15): Show |
18 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1533-1889_1533-188 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAA | 22 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(19): Show |
22 | HG00544.hp2 HG01081.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1533-1890_1533-188 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAA | 32 | a0001c0001t0003g0201 a0001c0001t0003g0203 a0001c0001t0003g0210 others(29): Show |
32 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1533-1891_1533-188 others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAAA | 13 | a0001c0001t0003g0251 a0001c0001t0003g0256 a0001c0001t0011g0277 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1533-1892_1533-188 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0003g0202 a0001c0001t0023g0252 a0001c0006t0011g0280 others(6): Show |
9 | HG01109.hp1 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-1893_1533-188 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0011g0189 a0001c0001t0046g0188 a0001c0006t0011g0281 others(8): Show |
11 | HG00733.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-1894_1533-188 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0011g0275 a0001c0001t0073g0276 a0003c0008t0016g0305 |
3 | HG02145.hp1 HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1533-1895_1533-188 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1533-1896_1533-188 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | CA | C | 6 | a0001c0001t0006g0096 a0001c0001t0009g0179 a0001c0001t0022g0005 others(3): Show |
7 | HG01433.hp1 HG01496.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-1886delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066452 | CAAAAAAA | C | 34 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(31): Show |
34 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1533-1892_1533-188 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | |||||||
chr9:109066573 | A | C | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1533-2006T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066573 | |||||||
chr9:109066613 | T | C | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-2046A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066613 | |||||||
chr9:109066732 | T | C | 1 | a0004c0003t0029g0056 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1533-2165A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066732 | |||||||
chr9:109066885 | G | A | 28 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(25): Show |
28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-2318C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066885 | |||||||
chr9:109067056 | C | CA | 136 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(133): Show |
136 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1533-2490dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067056 | |||||||
chr9:109067056 | CA | C | 6 | a0001c0001t0002g0076 a0001c0001t0004g0235 a0001c0001t0006g0096 others(3): Show |
6 | HG01074.hp1 HG01168.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-2490delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067056 | |||||||
chr9:109067083 | A | T | 3 | a0001c0001t0014g0183 a0001c0001t0049g0186 a0001c0001t0052g0185 |
3 | HG02109.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1533-2516T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067083 | |||||||
chr9:109067130 | T | C | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-2563A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067130 | |||||||
chr9:109067292 | G | A | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-2725C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067292 | |||||||
chr9:109067402 | T | G | 1 | a0003c0012t0063g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1533-2835A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067402 | |||||||
chr9:109067407 | A | T | 28 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(25): Show |
28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-2840T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067407 | |||||||
chr9:109067477 | T | G | 106 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(103): Show |
106 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1533-2910A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067477 | |||||||
chr9:109067512 | C | T | 80 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0002c0002t0001g0345 others(77): Show |
81 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1533-2945G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067512 | |||||||
chr9:109067779 | C | T | 1 | a0003c0012t0063g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1533-3212G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067779 | |||||||
chr9:109067821 | T | A | 2 | a0001c0001t0009g0107 a0001c0001t0059g0109 |
2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1533-3254A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067821 | |||||||
chr9:109067973 | A | G | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-3406T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067973 | |||||||
chr9:109068055 | A | G | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1533-3488T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068055 | |||||||
chr9:109068090 | G | A | 19 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533-3523C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068090 | |||||||
chr9:109068093 | C | T | 1 | a0001c0001t0005g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1533-3526G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068093 | |||||||
chr9:109068171 | T | C | 19 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533-3604A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068171 | |||||||
chr9:109068295 | G | A | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-3728C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068295 | |||||||
chr9:109068301 | C | T | 37 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(34): Show |
37 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1533-3734G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068301 | |||||||
chr9:109068369 | CA | C | 304 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(301): Show |
304 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(301): Show |
intron_variant | MODIFIER | c.1533-3803delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068369 | |||||||
chr9:109068411 | C | T | 5 | a0003c0004t0007g0336 a0003c0004t0007g0337 a0003c0004t0031g0331 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-3844G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068411 | |||||||
chr9:109068778 | T | C | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1533-4211A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068778 | |||||||
chr9:109068797 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-4230G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068797 | |||||||
chr9:109068823 | G | A | 1 | a0001c0001t0009g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1533-4256C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068823 | |||||||
chr9:109069175 | A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1532+4181T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069175 | |||||||
chr9:109069238 | A | G | 1 | a0001c0001t0035g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1532+4118T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069238 | |||||||
chr9:109069320 | G | A | 84 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(81): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1532+4036C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069320 | |||||||
chr9:109069545 | G | A | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3811C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069545 | |||||||
chr9:109069597 | C | T | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1532+3759G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069597 | |||||||
chr9:109069601 | T | C | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1532+3755A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069601 | |||||||
chr9:109069620 | C | T | 4 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0309 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+3736G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069620 | |||||||
chr9:109069661 | C | A | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1532+3695G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069661 | |||||||
chr9:109069912 | G | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3444C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069912 | |||||||
chr9:109070130 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+3226T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070130 | |||||||
chr9:109070175 | C | A | 1 | a0007c0014t0040g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1532+3181G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070175 | |||||||
chr9:109070191 | A | T | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3165T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070191 | |||||||
chr9:109070211 | C | T | 3 | a0002c0002t0001g0365 a0002c0002t0001g0397 a0002c0002t0001g0398 |
3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1532+3145G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070211 | |||||||
chr9:109070240 | C | T | 1 | a0003c0004t0071g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1532+3116G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070240 | |||||||
chr9:109070362 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+2994T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070362 | |||||||
chr9:109070406 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1532+2950C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070406 | |||||||
chr9:109070531 | C | A | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1532+2825G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070531 | |||||||
chr9:109070550 | G | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+2806C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070550 | |||||||
chr9:109070650 | TATG | T | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+2703_1532+270 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070650 | |||||||
chr9:109070779 | A | T | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+2577T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070779 | |||||||
chr9:109070849 | C | T | 1 | a0002c0002t0001g0370 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1532+2507G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070849 | |||||||
chr9:109070985 | G | A | 3 | a0001c0001t0012g0026 a0001c0001t0012g0027 a0001c0001t0012g0028 |
3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1532+2371C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070985 | |||||||
chr9:109071022 | C | T | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1532+2334G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071022 | |||||||
chr9:109071171 | C | T | 1 | a0001c0001t0034g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1532+2185G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071171 | |||||||
chr9:109071174 | C | T | 1 | a0001c0001t0004g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1532+2182G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071174 | |||||||
chr9:109071186 | A | T | 1 | a0001c0005t0003g0012 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1532+2170T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071186 | |||||||
chr9:109071231 | G | C | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1532+2125C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071231 | |||||||
chr9:109071466 | T | C | 13 | a0002c0002t0001g0365 a0002c0002t0001g0397 a0002c0002t0001g0398 others(10): Show |
13 | HG01433.hp2 HG02004.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1532+1890A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071466 | |||||||
chr9:109071511 | G | T | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532+1845C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071511 | |||||||
chr9:109071512 | G | A | 74 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532+1844C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071512 | |||||||
chr9:109071516 | A | G | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1840T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071516 | |||||||
chr9:109071518 | T | G | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1838A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071518 | |||||||
chr9:109071521 | T | A | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1835A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071521 | |||||||
chr9:109071538 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+1818T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071538 | |||||||
chr9:109071557 | T | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(52): Show |
56 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1532+1799A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071557 | |||||||
chr9:109071603 | C | CA | 135 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(132): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1532+1752dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071603 | |||||||
chr9:109071608 | A | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1532+1748T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071608 | |||||||
chr9:109071619 | A | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1532+1737T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071619 | |||||||
chr9:109071659 | T | A | 1 | a0002c0002t0001g0372 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1532+1697A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071659 | |||||||
chr9:109071923 | CTAGAGAG | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(54): Show |
59 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1532+1426_1532+143 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071923 | |||||||
chr9:109071926 | G | C | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+1430C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071926 | |||||||
chr9:109071941 | A | G | 2 | a0002c0002t0001g0372 a0002c0002t0018g0356 |
2 | NA18944.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1532+1415T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071941 | |||||||
chr9:109072025 | C | A | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1532+1331G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072025 | |||||||
chr9:109072189 | T | TTCCCATA others(17): Show |
1 | a0001c0001t0014g0248 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1532+1143_1532+116 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072189 | |||||||
chr9:109072493 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+863G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072493 | |||||||
chr9:109072658 | C | G | 2 | a0003c0004t0007g0326 a0003c0004t0007g0330 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1532+698G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072658 | |||||||
chr9:109072703 | G | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1532+653C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072703 | |||||||
chr9:109072754 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+602A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072754 | |||||||
chr9:109073125 | T | C | 1 | a0001c0001t0009g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1532+231A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073125 | |||||||
chr9:109073258 | A | C | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+98T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073258 | |||||||
chr9:109073334 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+22A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073334 | |||||||
chr9:109073344 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1532+12G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073344 | |||||||
chr9:109073614 | C | T | 3 | a0003c0004t0007g0312 a0003c0004t0007g0313 a0003c0004t0007g0343 |
3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-176G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073614 | |||||||
chr9:109073615 | G | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450-177C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073615 | |||||||
chr9:109073680 | A | G | 53 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(50): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1450-242T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073680 | |||||||
chr9:109073682 | A | T | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-244T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073682 | |||||||
chr9:109073716 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1450-278A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073716 | |||||||
chr9:109073745 | G | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1450-307C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073745 | |||||||
chr9:109073833 | T | C | 3 | a0001c0006t0041g0286 a0001c0006t0041g0287 a0001c0006t0061g0288 |
3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1450-395A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073833 | |||||||
chr9:109073844 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0001c0001t0003g0258 others(2): Show |
5 | NA18986.hp1 NA19057.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450-421_1450-407d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073844 | |||||||
chr9:109073853 | T | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0002c0002t0018g0350 others(1): Show |
5 | HG00621.hp1 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-415A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073853 | |||||||
chr9:109073856 | G | GT | 139 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(136): Show |
140 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1450-419dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | |||||||
chr9:109073856 | G | GTT | 13 | a0001c0001t0002g0046 a0001c0001t0002g0190 a0001c0016t0012g0293 others(10): Show |
13 | HG00733.hp1 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1450-420_1450-419d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | |||||||
chr9:109073856 | G | GTTT | 20 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1450-421_1450-419d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | |||||||
chr9:109073856 | G | T | 5 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 others(2): Show |
5 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-418C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | |||||||
chr9:109073864 | T | G | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1450-426A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073864 | |||||||
chr9:109073865 | T | G | 48 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0004g0193 others(45): Show |
48 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1450-427A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073865 | |||||||
chr9:109073867 | T | G | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-429A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073867 | |||||||
chr9:109073903 | C | A | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-465G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073903 | |||||||
chr9:109073978 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1450-540T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073978 | |||||||
chr9:109074104 | T | C | 27 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(24): Show |
27 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-666A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074104 | |||||||
chr9:109074110 | T | C | 1 | a0001c0001t0008g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1450-672A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074110 | |||||||
chr9:109074269 | T | C | 1 | a0001c0001t0004g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1450-831A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074269 | |||||||
chr9:109074299 | C | T | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1450-861G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074299 | |||||||
chr9:109074386 | C | T | 1 | a0001c0001t0006g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1450-948G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074386 | |||||||
chr9:109074391 | C | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-953G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074391 | |||||||
chr9:109074462 | G | T | 8 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0001c0001t0003g0257 others(5): Show |
8 | NA18964.hp2 NA18986.hp1 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.1450-1024C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074462 | |||||||
chr9:109074477 | A | G | 4 | a0002c0002t0001g0371 a0002c0002t0001g0382 a0002c0002t0001g0383 others(1): Show |
4 | HG00735.hp2 HG01515.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-1039T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074477 | |||||||
chr9:109074479 | G | A | 4 | a0002c0002t0001g0371 a0002c0002t0001g0382 a0002c0002t0001g0383 others(1): Show |
4 | HG00735.hp2 HG01515.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-1041C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074479 | |||||||
chr9:109074524 | G | A | 2 | a0001c0001t0009g0107 a0001c0001t0059g0109 |
2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1450-1086C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074524 | |||||||
chr9:109074661 | G | A | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1450-1223C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074661 | |||||||
chr9:109074715 | G | A | 1 | a0001c0001t0065g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1450-1277C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074715 | |||||||
chr9:109074785 | C | T | 37 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(34): Show |
37 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1450-1347G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074785 | |||||||
chr9:109074814 | G | A | 37 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(34): Show |
37 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1450-1376C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074814 | |||||||
chr9:109074837 | C | T | 2 | a0001c0001t0020g0131 a0001c0001t0020g0132 |
2 | NA18968.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1450-1399G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074837 | |||||||
chr9:109074952 | C | T | 1 | a0001c0001t0040g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1450-1514G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074952 | |||||||
chr9:109074960 | T | A | 1 | a0001c0001t0012g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1450-1522A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074960 | |||||||
chr9:109075025 | T | A | 3 | a0001c0001t0006g0090 a0001c0001t0006g0100 a0001c0001t0028g0079 |
3 | HG03834.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1450-1587A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075025 | |||||||
chr9:109075030 | C | T | 1 | a0001c0001t0009g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1450-1592G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075030 | |||||||
chr9:109075088 | G | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450-1650C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075088 | |||||||
chr9:109075112 | T | C | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1450-1674A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075112 | |||||||
chr9:109075214 | C | T | 6 | a0001c0001t0014g0183 a0001c0001t0014g0187 a0001c0001t0014g0233 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450-1776G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075214 | |||||||
chr9:109075290 | T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1450-1852A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075290 | |||||||
chr9:109075366 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1450-1928A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075366 | |||||||
chr9:109075496 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1450-2058A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075496 | |||||||
chr9:109075511 | A | T | 139 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1450-2073T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075511 | |||||||
chr9:109075584 | A | T | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1450-2146T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075584 | |||||||
chr9:109075751 | G | A | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1450-2313C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075751 | |||||||
chr9:109076185 | T | C | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-2747A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076185 | |||||||
chr9:109076255 | C | CCAT | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1450-2820_1450-281 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076255 | |||||||
chr9:109076312 | T | C | 27 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(24): Show |
27 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-2874A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076312 | |||||||
chr9:109076322 | C | A | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1450-2884G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076322 | |||||||
chr9:109076385 | TG | T | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1450-2948delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076385 | |||||||
chr9:109076435 | A | G | 1 | a0001c0001t0075g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1450-2997T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076435 | |||||||
chr9:109076443 | T | A | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1450-3005A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076443 | |||||||
chr9:109076470 | C | T | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1450-3032G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076470 | |||||||
chr9:109076530 | TA | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-3093delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076530 | |||||||
chr9:109076530 | TAA | T | 27 | a0001c0001t0065g0029 a0003c0004t0007g0312 a0003c0004t0007g0313 others(24): Show |
27 | HG00099.hp2 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-3094_1450-309 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076530 | |||||||
chr9:109076538 | A | G | 1 | a0001c0001t0003g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1450-3100T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076538 | |||||||
chr9:109076602 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1450-3164C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076602 | |||||||
chr9:109076752 | G | A | 1 | a0001c0007t0004g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1450-3314C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076752 | |||||||
chr9:109076846 | A | G | 1 | a0001c0001t0043g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1450-3408T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076846 | |||||||
chr9:109076971 | G | A | 1 | a0001c0001t0051g0244 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1450-3533C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076971 | |||||||
chr9:109077132 | C | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1450-3694G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077132 | |||||||
chr9:109077142 | T | C | 1 | a0002c0002t0001g0391 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1449+3697A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077142 | |||||||
chr9:109077226 | C | T | 26 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0102 others(23): Show |
26 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(23): Show |
intron_variant | MODIFIER | c.1449+3613G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077226 | |||||||
chr9:109077401 | C | T | 2 | a0003c0004t0007g0337 a0003c0004t0083g0332 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1449+3438G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077401 | |||||||
chr9:109077466 | T | C | 8 | a0001c0001t0011g0189 a0001c0001t0046g0188 a0001c0006t0011g0280 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1449+3373A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077466 | |||||||
chr9:109077669 | T | A | 51 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(48): Show |
51 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1449+3170A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077669 | |||||||
chr9:109077873 | T | C | 2 | a0001c0001t0005g0140 a0001c0001t0005g0142 |
2 | NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1449+2966A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077873 | |||||||
chr9:109077956 | G | C | 1 | a0003c0004t0042g0314 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1449+2883C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077956 | |||||||
chr9:109078097 | T | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+2742A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078097 | |||||||
chr9:109078220 | C | T | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1449+2619G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078220 | |||||||
chr9:109078302 | TAAAAG | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+2532_1449+253 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078302 | |||||||
chr9:109078352 | T | A | 1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1449+2487A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078352 | |||||||
chr9:109078353 | C | T | 1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1449+2486G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078353 | |||||||
chr9:109078382 | A | C | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1449+2457T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078382 | |||||||
chr9:109078518 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1449+2321T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078518 | |||||||
chr9:109078619 | T | C | 1 | a0002c0002t0018g0396 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1449+2220A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078619 | |||||||
chr9:109078690 | G | A | 1 | a0001c0005t0024g0011 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1449+2149C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078690 | |||||||
chr9:109078732 | T | C | 6 | a0001c0001t0004g0182 a0001c0001t0009g0179 a0001c0001t0009g0180 others(3): Show |
6 | HG04204.hp2 NA18946.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+2107A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078732 | |||||||
chr9:109078874 | T | A | 28 | a0001c0001t0011g0189 a0001c0001t0011g0277 a0001c0001t0011g0278 others(25): Show |
28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+1965A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078874 | |||||||
chr9:109078896 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1449+1943A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078896 | |||||||
chr9:109078937 | A | G | 6 | a0001c0001t0014g0183 a0001c0001t0014g0187 a0001c0001t0014g0233 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+1902T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078937 | |||||||
chr9:109079014 | T | C | 3 | a0001c0001t0007g0030 a0003c0004t0007g0329 a0003c0004t0007g0341 |
3 | HG00099.hp2 HG00140.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1449+1825A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079014 | |||||||
chr9:109079019 | A | G | 1 | a0001c0001t0039g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1449+1820T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079019 | |||||||
chr9:109079082 | T | C | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1449+1757A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079082 | |||||||
chr9:109079212 | T | C | 192 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1449+1627A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079212 | |||||||
chr9:109079218 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+1621A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079218 | |||||||
chr9:109079314 | C | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+1525G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079314 | |||||||
chr9:109079496 | A | G | 6 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(3): Show |
6 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+1343T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079496 | |||||||
chr9:109079508 | G | A | 1 | a0003c0008t0016g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1449+1331C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079508 | |||||||
chr9:109079901 | T | C | 5 | a0001c0001t0048g0006 a0001c0006t0030g0289 a0001c0006t0030g0290 others(2): Show |
5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+938A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079901 | |||||||
chr9:109079914 | A | C | 225 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(222): Show |
226 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.1449+925T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079914 | |||||||
chr9:109080137 | T | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1449+702A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080137 | |||||||
chr9:109080246 | C | T | 1 | a0001c0001t0073g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1449+593G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080246 | |||||||
chr9:109080256 | G | T | 1 | a0001c0001t0004g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1449+583C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080256 | |||||||
chr9:109080522 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1449+317T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080522 | |||||||
chr9:109080551 | TA | T | 4 | a0001c0001t0008g0160 a0001c0001t0008g0162 a0001c0001t0008g0163 others(1): Show |
4 | HG01192.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+287delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080551 | |||||||
chr9:109080572 | GTTC | G | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1449+264_1449+266d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080572 | |||||||
chr9:109080620 | C | T | 1 | a0002c0002t0001g0403 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1449+219G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080620 | |||||||
chr9:109080637 | A | C | 1 | a0001c0001t0012g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+202T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080637 | |||||||
chr9:109080756 | GCC | G | 19 | a0001c0001t0011g0189 a0001c0001t0011g0277 a0001c0001t0011g0278 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1449+81_1449+82del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080756 | |||||||
chr9:109080775 | A | T | 416 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(413): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.1449+64T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080775 | |||||||
chr9:109081326 | A | C | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1345-383T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081326 | |||||||
chr9:109081332 | G | A | 9 | a0002c0002t0001g0411 a0002c0002t0001g0412 a0002c0002t0001g0413 others(6): Show |
9 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-389C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081332 | |||||||
chr9:109081614 | G | C | 1 | a0001c0001t0019g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1345-671C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081614 | |||||||
chr9:109081615 | G | A | 1 | a0003c0004t0007g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1345-672C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081615 | |||||||
chr9:109081625 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1345-682A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081625 | |||||||
chr9:109081682 | A | G | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1345-739T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081682 | |||||||
chr9:109081913 | TGATA | T | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1345-974_1345-971d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081913 | |||||||
chr9:109081920 | T | C | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1345-977A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081920 | |||||||
chr9:109081966 | C | A | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1345-1023G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081966 | |||||||
chr9:109082302 | G | A | 6 | a0002c0002t0001g0351 a0002c0002t0001g0384 a0002c0002t0001g0385 others(3): Show |
6 | HG00621.hp1 NA18973.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-1359C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082302 | |||||||
chr9:109082336 | CT | C | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1345-1394delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082336 | |||||||
chr9:109082427 | T | C | 7 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(4): Show |
7 | NA18948.hp2 NA18952.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-1484A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082427 | |||||||
chr9:109082443 | T | C | 1 | a0001c0007t0004g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1345-1500A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082443 | |||||||
chr9:109082444 | T | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1345-1501A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082444 | |||||||
chr9:109082533 | G | A | 16 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0046g0188 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1345-1590C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082533 | |||||||
chr9:109082568 | C | A | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1345-1625G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082568 | |||||||
chr9:109082638 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1345-1695A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082638 | |||||||
chr9:109082650 | A | AT | 6 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 others(3): Show |
6 | HG00438.hp2 HG00735.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-1708dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | |||||||
chr9:109082650 | AT | A | 93 | a0001c0001t0003g0215 a0001c0001t0004g0082 a0001c0001t0004g0182 others(90): Show |
93 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1345-1708delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | |||||||
chr9:109082650 | ATT | A | 111 | a0001c0001t0007g0030 a0001c0001t0043g0127 a0001c0001t0045g0174 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1345-1709_1345-170 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | |||||||
chr9:109082784 | T | C | 1 | a0003c0008t0016g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1345-1841A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082784 | |||||||
chr9:109083128 | C | T | 2 | a0003c0004t0007g0337 a0003c0004t0083g0332 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1345-2185G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083128 | |||||||
chr9:109083173 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1345-2230T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083173 | |||||||
chr9:109083175 | T | C | 192 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1345-2232A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083175 | |||||||
chr9:109083176 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1345-2233C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083176 | |||||||
chr9:109083223 | C | G | 191 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1345-2280G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083223 | |||||||
chr9:109083280 | G | A | 1 | a0001c0001t0025g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1345-2337C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083280 | |||||||
chr9:109083298 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1345-2355C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083298 | |||||||
chr9:109083336 | C | T | 1 | a0003c0004t0031g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1345-2393G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083336 | |||||||
chr9:109083357 | C | T | 2 | a0001c0001t0003g0210 a0003c0004t0081g0342 |
2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1345-2414G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083357 | |||||||
chr9:109083492 | G | A | 53 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1344+2505C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083492 | |||||||
chr9:109083518 | G | A | 35 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(32): Show |
35 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1344+2479C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083518 | |||||||
chr9:109083899 | T | TACAAAAA others(6): Show |
1 | a0001c0001t0005g0130 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1344+2085_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083899 | |||||||
chr9:109083901 | C | CA | 11 | a0001c0001t0008g0161 a0001c0001t0033g0165 a0001c0001t0038g0172 others(8): Show |
11 | HG01106.hp1 HG01515.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344+2095dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAA | 52 | a0001c0001t0034g0158 a0001c0001t0045g0176 a0001c0006t0041g0286 others(49): Show |
52 | HG00099.hp1 HG00438.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1344+2094_1344+209 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAA | 29 | a0001c0001t0045g0174 a0001c0006t0041g0287 a0001c0006t0061g0288 others(26): Show |
29 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1344+2093_1344+209 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAA | 9 | a0001c0001t0011g0275 a0001c0001t0048g0006 a0001c0006t0011g0282 others(6): Show |
9 | HG01099.hp2 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+2092_1344+209 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAA | 9 | a0001c0001t0011g0277 a0001c0001t0011g0278 a0001c0001t0046g0188 others(6): Show |
9 | HG01243.hp1 HG01261.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+2091_1344+209 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(1): Show |
42 | a0001c0001t0002g0076 a0001c0001t0004g0193 a0001c0001t0004g0194 others(39): Show |
42 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1344+2088_1344+209 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(2): Show |
45 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0003g0215 others(42): Show |
45 | HG00621.hp2 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1344+2087_1344+209 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(3): Show |
22 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0035 others(19): Show |
23 | HG00408.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+2086_1344+209 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0004g0225 others(1): Show |
4 | HG00140.hp1 HG01496.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2085_1344+209 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0049 a0001c0001t0012g0026 a0001c0001t0012g0027 others(1): Show |
4 | HG00741.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2084_1344+209 others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0036g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1344+2078_1344+209 others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0055g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1344+2074_1344+209 others(26): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0012g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1344+2071_1344+209 others(29): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAAAAA others(6): Show |
6 | a0001c0005t0003g0007 a0001c0005t0003g0009 a0001c0005t0003g0010 others(3): Show |
6 | HG01978.hp2 HG02273.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+2095_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | C | CAAAACAA others(6): Show |
2 | a0001c0005t0003g0014 a0001c0005t0003g0015 |
2 | NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1344+2095_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAA | C | 6 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0086 others(3): Show |
6 | HG02027.hp2 HG02074.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+2093_1344+209 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAA | C | 11 | a0001c0001t0002g0043 a0001c0001t0004g0117 a0001c0001t0006g0084 others(8): Show |
11 | HG00544.hp1 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344+2092_1344+209 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAAA | C | 16 | a0001c0001t0002g0042 a0001c0001t0006g0085 a0001c0001t0006g0088 others(13): Show |
17 | HG00558.hp2 HG01255.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+2091_1344+209 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0003g0201 a0001c0001t0003g0203 a0001c0001t0003g0204 others(28): Show |
31 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1344+2087_1344+209 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1344+2086_1344+209 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAAAAA others(4): Show |
C | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+2085_1344+209 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083901 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0056g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1344+2080_1344+209 others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | |||||||
chr9:109083902 | A | AAAAAAAA others(6): Show |
4 | a0001c0005t0023g0013 a0001c0005t0024g0011 a0001c0005t0024g0017 others(1): Show |
4 | HG02015.hp2 HG02040.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2094_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083902 | |||||||
chr9:109083911 | A | C | 1 | a0001c0005t0003g0008 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1344+2086T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083911 | |||||||
chr9:109083915 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0005g0121 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1344+2067_1344+208 others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083915 | |||||||
chr9:109083915 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0043g0122 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1344+2081_1344+208 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083915 | |||||||
chr9:109083916 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0005g0142 a0001c0005t0003g0020 |
2 | NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083916 | A | AAAAAAAA others(7): Show |
8 | a0001c0001t0005g0139 a0001c0001t0005g0140 a0001c0001t0005g0141 others(5): Show |
8 | HG01099.hp1 HG02602.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+2067_1344+208 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083916 | A | AAAAAAAA others(6): Show |
25 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0133 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083916 | A | AAAAAAAA others(6): Show |
1 | a0001c0005t0003g0008 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083916 | A | ACAAAAAA others(6): Show |
2 | a0001c0001t0005g0129 a0001c0001t0005g0152 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083916 | A | C | 13 | a0001c0001t0005g0130 a0001c0005t0003g0007 a0001c0005t0003g0009 others(10): Show |
13 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1344+2081T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | |||||||
chr9:109083925 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0009g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(34): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(33): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0059g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(31): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0009g0108 a0001c0001t0009g0113 |
2 | NA18999.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(30): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0009g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(27): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0009g0107 a0001c0001t0036g0181 |
2 | HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(26): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0009g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0009g0180 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(23): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(11): Show |
4 | a0001c0001t0009g0179 a0001c0001t0012g0110 a0001c0001t0012g0178 others(1): Show |
4 | NA18946.hp2 NA18963.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083925 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0004g0082 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | |||||||
chr9:109083990 | T | C | 3 | a0003c0004t0007g0336 a0003c0004t0031g0331 a0003c0004t0031g0333 |
3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1344+2007A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083990 | |||||||
chr9:109084044 | A | G | 5 | a0001c0001t0048g0006 a0001c0006t0030g0289 a0001c0006t0030g0290 others(2): Show |
5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+1953T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084044 | |||||||
chr9:109084084 | T | TA | 207 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(204): Show |
208 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.1344+1912dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084084 | |||||||
chr9:109084084 | TA | T | 26 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1344+1912delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084084 | |||||||
chr9:109084445 | G | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1344+1552C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084445 | |||||||
chr9:109084810 | T | G | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1344+1187A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084810 | |||||||
chr9:109084828 | T | C | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1344+1169A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084828 | |||||||
chr9:109085240 | G | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+757C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085240 | |||||||
chr9:109085360 | T | C | 2 | a0001c0001t0051g0244 a0001c0001t0053g0197 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1344+637A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085360 | |||||||
chr9:109085416 | A | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+581T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085416 | |||||||
chr9:109085455 | T | C | 1 | a0001c0001t0022g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1344+542A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085455 | |||||||
chr9:109085464 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+533T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085464 | |||||||
chr9:109085540 | A | G | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1344+457T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085540 | |||||||
chr9:109085653 | A | G | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1344+344T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085653 | |||||||
chr9:109085720 | A | G | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+277T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085720 | |||||||
chr9:109085944 | C | T | 3 | a0001c0005t0003g0014 a0001c0005t0003g0015 a0001c0005t0003g0016 |
3 | NA18945.hp1 NA18979.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1344+53G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085944 | |||||||
chr9:109086029 | T | TA | 11 | a0001c0001t0011g0189 a0001c0001t0011g0277 a0001c0001t0011g0278 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321-10dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086029 | |||||||
chr9:109086120 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-100C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086120 | |||||||
chr9:109086120 | GGAAACCA others(5): Show |
G | 1 | a0002c0002t0001g0366 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1321-112_1321-101d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086120 | |||||||
chr9:109086190 | G | A | 33 | a0001c0001t0007g0030 a0001c0001t0045g0174 a0001c0001t0045g0176 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1321-170C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086190 | |||||||
chr9:109086222 | T | C | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1321-202A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086222 | |||||||
chr9:109086279 | T | C | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1321-259A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086279 | |||||||
chr9:109086294 | T | C | 5 | a0001c0001t0008g0160 a0001c0001t0008g0162 a0001c0001t0008g0163 others(2): Show |
5 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321-274A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086294 | |||||||
chr9:109086311 | T | G | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1321-291A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086311 | |||||||
chr9:109086348 | A | T | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1321-328T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086348 | |||||||
chr9:109086369 | G | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-349C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086369 | |||||||
chr9:109086399 | C | T | 1 | a0001c0001t0069g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1321-379G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086399 | |||||||
chr9:109086407 | GC | G | 3 | a0003c0004t0007g0336 a0003c0004t0031g0331 a0003c0004t0031g0333 |
3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1321-388delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086407 | |||||||
chr9:109086427 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-407C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086427 | |||||||
chr9:109086478 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1321-458A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086478 | |||||||
chr9:109086500 | T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1321-480A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086500 | |||||||
chr9:109086513 | A | G | 1 | a0001c0001t0009g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1321-493T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086513 | |||||||
chr9:109086514 | T | C | 1 | a0003c0004t0007g0330 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1321-494A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086514 | |||||||
chr9:109086539 | A | G | 139 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1321-519T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086539 | |||||||
chr9:109086598 | G | C | 1 | a0001c0001t0075g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1320+575C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086598 | |||||||
chr9:109086613 | T | G | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1320+560A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086613 | |||||||
chr9:109086661 | G | A | 11 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(8): Show |
11 | HG00544.hp2 HG02273.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.1320+512C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086661 | |||||||
chr9:109086817 | A | G | 1 | a0001c0001t0065g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1320+356T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086817 | |||||||
chr9:109086892 | C | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1320+281G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086892 | |||||||
chr9:109086920 | A | G | 11 | a0001c0001t0009g0077 a0001c0001t0014g0183 a0001c0001t0014g0187 others(8): Show |
11 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1320+253T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086920 | |||||||
chr9:109086977 | C | T | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1320+196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086977 | |||||||
chr9:109087012 | T | A | 1 | a0001c0001t0008g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1320+161A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109087012 | |||||||
chr9:109087066 | T | A | 1 | a0001c0001t0003g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1320+107A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109087066 | |||||||
chr9:109087363 | C | G | 1 | a0001c0006t0030g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1151-21G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087363 | |||||||
chr9:109087452 | T | G | 40 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(37): Show |
40 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1151-110A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087452 | |||||||
chr9:109087514 | T | A | 1 | a0001c0001t0005g0143 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1151-172A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087514 | |||||||
chr9:109087627 | A | T | 1 | a0001c0001t0054g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1151-285T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087627 | |||||||
chr9:109087635 | C | T | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-293G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087635 | |||||||
chr9:109087770 | T | C | 1 | a0001c0001t0012g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1151-428A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087770 | |||||||
chr9:109087897 | G | A | 1 | a0001c0006t0011g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-555C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087897 | |||||||
chr9:109087971 | G | C | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1151-629C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087971 | |||||||
chr9:109088157 | C | A | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1151-815G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088157 | |||||||
chr9:109088298 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-956T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088298 | |||||||
chr9:109088386 | C | T | 2 | a0003c0004t0017g0324 a0003c0004t0017g0325 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1151-1044G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088386 | |||||||
chr9:109088409 | A | G | 1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1151-1067T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088409 | |||||||
chr9:109088419 | G | A | 1 | a0001c0001t0028g0081 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1151-1077C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088419 | |||||||
chr9:109088430 | A | G | 139 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1151-1088T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088430 | |||||||
chr9:109088605 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1263T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088605 | |||||||
chr9:109088627 | G | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1151-1285C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088627 | |||||||
chr9:109088661 | C | T | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1151-1319G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088661 | |||||||
chr9:109088678 | G | A | 1 | a0001c0001t0040g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1151-1336C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088678 | |||||||
chr9:109088730 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1388T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088730 | |||||||
chr9:109088760 | G | A | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1151-1418C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088760 | |||||||
chr9:109088809 | A | C | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1467T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088809 | |||||||
chr9:109088815 | C | CA | 11 | a0001c0001t0003g0214 a0001c0001t0011g0277 a0001c0001t0012g0178 others(8): Show |
11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1151-1474dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | |||||||
chr9:109088815 | CA | C | 30 | a0001c0001t0003g0201 a0001c0001t0003g0215 a0001c0001t0004g0195 others(27): Show |
30 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1151-1474delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | |||||||
chr9:109088815 | CAA | C | 33 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(30): Show |
34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1151-1475_1151-147 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | |||||||
chr9:109088815 | CAAA | C | 50 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(47): Show |
51 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1151-1476_1151-147 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | |||||||
chr9:109088842 | G | C | 2 | a0001c0001t0009g0113 a0001c0001t0012g0110 |
2 | NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1151-1500C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088842 | |||||||
chr9:109088897 | G | GC | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1151-1556dupG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088897 | |||||||
chr9:109088996 | G | A | 15 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 others(12): Show |
15 | HG00544.hp2 HG02273.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.1151-1654C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088996 | |||||||
chr9:109089053 | T | A | 139 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1151-1711A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089053 | |||||||
chr9:109089132 | G | A | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1150+1790C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089132 | |||||||
chr9:109089194 | G | C | 21 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0102 others(18): Show |
21 | HG00609.hp2 HG02132.hp2 HG04204.hp2 others(18): Show |
intron_variant | MODIFIER | c.1150+1728C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089194 | |||||||
chr9:109089226 | C | G | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1150+1696G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089226 | |||||||
chr9:109089227 | T | C | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1150+1695A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089227 | |||||||
chr9:109089233 | CA | C | 77 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1150+1688delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089233 | |||||||
chr9:109089242 | A | C | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1150+1680T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089242 | |||||||
chr9:109089475 | T | G | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1150+1447A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089475 | |||||||
chr9:109089622 | A | T | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1150+1300T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089622 | |||||||
chr9:109089850 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1150+1072T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089850 | |||||||
chr9:109090215 | C | G | 13 | a0001c0005t0003g0007 a0001c0005t0003g0008 a0001c0005t0003g0009 others(10): Show |
13 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1150+707G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090215 | |||||||
chr9:109090233 | C | G | 1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1150+689G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090233 | |||||||
chr9:109090248 | G | A | 4 | a0002c0002t0001g0365 a0002c0002t0001g0397 a0002c0002t0001g0398 others(1): Show |
4 | HG03669.hp1 NA18949.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+674C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090248 | |||||||
chr9:109090260 | CA | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+661delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090260 | |||||||
chr9:109090270 | A | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1150+652T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090270 | |||||||
chr9:109090371 | T | C | 1 | a0004c0003t0029g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1150+551A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090371 | |||||||
chr9:109090446 | G | A | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1150+476C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090446 | |||||||
chr9:109090451 | G | A | 1 | a0002c0002t0001g0354 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1150+471C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090451 | |||||||
chr9:109090625 | G | A | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1150+297C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090625 | |||||||
chr9:109090716 | C | CA | 74 | a0001c0001t0003g0258 a0001c0001t0038g0169 a0002c0002t0001g0345 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1150+205dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090716 | |||||||
chr9:109090716 | CA | C | 29 | a0001c0001t0004g0231 a0001c0001t0007g0030 a0001c0001t0065g0029 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1150+205delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090716 | |||||||
chr9:109090774 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1150+148C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090774 | |||||||
chr9:109090868 | G | GA | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+53dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090868 | |||||||
chr9:109090898 | G | A | 1 | a0001c0001t0006g0096 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1150+24C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090898 | |||||||
chr9:109090902 | G | A | 2 | a0003c0004t0081g0342 a0003c0017t0082g0311 |
2 | HG03669.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1150+20C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090902 | |||||||
chr9:109091199 | T | C | 1 | a0003c0004t0007g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.917-44A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091199 | |||||||
chr9:109091266 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.917-111A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091266 | |||||||
chr9:109091406 | A | G | 402 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(399): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.917-251T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091406 | |||||||
chr9:109091482 | C | G | 1 | a0001c0001t0004g0195 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.917-327G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091482 | |||||||
chr9:109091496 | T | C | 1 | a0001c0001t0005g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.917-341A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091496 | |||||||
chr9:109091565 | A | G | 1 | a0001c0001t0004g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.917-410T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091565 | |||||||
chr9:109091574 | A | G | 1 | a0001c0001t0006g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.917-419T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091574 | |||||||
chr9:109091669 | G | A | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.917-514C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091669 | |||||||
chr9:109091683 | G | A | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.917-528C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091683 | |||||||
chr9:109091705 | T | C | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.917-550A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091705 | |||||||
chr9:109091885 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.917-730A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091885 | |||||||
chr9:109091900 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.917-745A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091900 | |||||||
chr9:109091957 | G | A | 1 | a0003c0004t0007g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.917-802C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091957 | |||||||
chr9:109091966 | G | A | 51 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(48): Show |
51 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.917-811C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091966 | |||||||
chr9:109091985 | A | C | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.917-830T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091985 | |||||||
chr9:109092099 | T | C | 3 | a0001c0001t0005g0145 a0001c0001t0005g0146 a0001c0001t0005g0147 |
3 | HG01081.hp1 HG01257.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.917-944A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092099 | |||||||
chr9:109092110 | T | C | 29 | a0001c0001t0007g0030 a0001c0001t0039g0044 a0001c0001t0065g0029 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.917-955A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092110 | |||||||
chr9:109092134 | T | G | 12 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.917-979A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092134 | |||||||
chr9:109092204 | A | G | 1 | a0001c0001t0084g0420 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.917-1049T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092204 | |||||||
chr9:109092326 | TA | T | 416 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(413): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.916+1148delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092326 | |||||||
chr9:109092343 | A | G | 1 | a0001c0006t0011g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.916+1132T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092343 | |||||||
chr9:109092388 | C | A | 2 | a0003c0004t0007g0337 a0003c0004t0083g0332 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.916+1087G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092388 | |||||||
chr9:109092805 | A | G | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.916+670T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092805 | |||||||
chr9:109092899 | G | A | 2 | a0002c0002t0001g0361 a0002c0002t0001g0364 |
2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.916+576C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092899 | |||||||
chr9:109092925 | T | C | 1 | a0001c0001t0045g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.916+550A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092925 | |||||||
chr9:109092949 | CAG | C | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.916+524_916+525del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092949 | |||||||
chr9:109093285 | C | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.916+190G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093285 | |||||||
chr9:109093349 | C | A | 2 | a0004c0003t0002g0038 a0004c0003t0002g0069 |
2 | HG02056.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.916+126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093349 | |||||||
chr9:109093459 | C | T | 1 | a0001c0001t0034g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.916+16G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093459 | |||||||
chr9:109093613 | T | G | 4 | a0001c0001t0006g0084 a0001c0001t0006g0085 a0001c0001t0006g0086 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-22A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109093613 | |||||||
chr9:109093993 | G | C | 1 | a0001c0001t0004g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.800-402C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109093993 | |||||||
chr9:109094041 | G | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.800-450C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094041 | |||||||
chr9:109094098 | G | A | 1 | a0001c0001t0015g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.800-507C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094098 | |||||||
chr9:109094271 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.800-680T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094271 | |||||||
chr9:109094418 | G | A | 1 | a0001c0001t0028g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.800-827C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094418 | |||||||
chr9:109094452 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-861T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094452 | |||||||
chr9:109094476 | A | C | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.800-885T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094476 | |||||||
chr9:109094808 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.800-1217G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094808 | |||||||
chr9:109094947 | C | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-1356G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094947 | |||||||
chr9:109094969 | T | A | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1378A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094969 | |||||||
chr9:109095070 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-1479C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095070 | |||||||
chr9:109095111 | G | A | 367 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(364): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.800-1520C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095111 | |||||||
chr9:109095160 | C | G | 190 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.800-1569G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095160 | |||||||
chr9:109095285 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.800-1694C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095285 | |||||||
chr9:109095353 | C | T | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1762G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095353 | |||||||
chr9:109095395 | G | A | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1804C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095395 | |||||||
chr9:109095396 | A | C | 53 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(50): Show |
53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.800-1805T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095396 | |||||||
chr9:109095585 | T | G | 17 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(14): Show |
17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-1994A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095585 | |||||||
chr9:109095754 | G | C | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.800-2163C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095754 | |||||||
chr9:109095765 | G | A | 25 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-2174C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095765 | |||||||
chr9:109095871 | A | G | 2 | a0003c0012t0063g0022 a0003c0018t0066g0307 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.800-2280T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095871 | |||||||
chr9:109096079 | C | T | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2488G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096079 | |||||||
chr9:109096114 | G | C | 1 | a0001c0001t0005g0125 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.800-2523C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096114 | |||||||
chr9:109096119 | T | A | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2528A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096119 | |||||||
chr9:109096122 | A | G | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2531T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096122 | |||||||
chr9:109096252 | G | A | 1 | a0002c0002t0010g0399 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.800-2661C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096252 | |||||||
chr9:109096286 | C | T | 3 | a0001c0001t0027g0199 a0001c0001t0027g0211 a0001c0001t0027g0260 |
3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.800-2695G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096286 | |||||||
chr9:109096349 | C | T | 1 | a0001c0001t0023g0252 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.800-2758G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096349 | |||||||
chr9:109096419 | G | A | 2 | a0002c0002t0001g0361 a0002c0002t0001g0364 |
2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.800-2828C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096419 | |||||||
chr9:109096420 | T | C | 53 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(50): Show |
53 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.800-2829A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096420 | |||||||
chr9:109096426 | G | A | 3 | a0001c0005t0003g0007 a0001c0005t0003g0008 a0001c0005t0003g0009 |
3 | NA19011.hp1 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.800-2835C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096426 | |||||||
chr9:109096947 | A | C | 1 | a0001c0001t0012g0178 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.800-3356T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096947 | |||||||
chr9:109096955 | G | A | 1 | a0001c0001t0004g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.800-3364C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096955 | |||||||
chr9:109097018 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-3427C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097018 | |||||||
chr9:109097043 | T | G | 53 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(50): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.800-3452A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097043 | |||||||
chr9:109097158 | A | T | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3567T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097158 | |||||||
chr9:109097266 | A | G | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3675T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097266 | |||||||
chr9:109097281 | C | T | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3690G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097281 | |||||||
chr9:109097335 | A | T | 1 | a0001c0001t0020g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.800-3744T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097335 | |||||||
chr9:109097374 | G | GT | 8 | a0001c0001t0004g0235 a0001c0007t0004g0297 a0001c0007t0004g0298 others(5): Show |
8 | HG01074.hp1 HG02735.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.800-3784dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097374 | |||||||
chr9:109097389 | G | A | 1 | a0001c0001t0065g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.800-3798C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097389 | |||||||
chr9:109097467 | A | T | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.800-3876T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097467 | |||||||
chr9:109097503 | A | G | 17 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(14): Show |
17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-3912T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097503 | |||||||
chr9:109097544 | C | T | 1 | a0002c0002t0010g0369 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.800-3953G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097544 | |||||||
chr9:109097552 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0045 a0001c0001t0002g0046 |
4 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3961G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097552 | |||||||
chr9:109097559 | T | C | 11 | a0001c0001t0045g0174 a0001c0001t0045g0176 a0003c0008t0016g0304 others(8): Show |
11 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-3968A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097559 | |||||||
chr9:109097565 | T | C | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3974A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097565 | |||||||
chr9:109097636 | T | C | 25 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-4045A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097636 | |||||||
chr9:109097744 | C | T | 1 | a0001c0001t0009g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.800-4153G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097744 | |||||||
chr9:109097789 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.800-4198G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097789 | |||||||
chr9:109097813 | T | C | 1 | a0001c0001t0022g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.800-4222A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097813 | |||||||
chr9:109097905 | A | C | 139 | a0001c0001t0007g0030 a0001c0001t0011g0189 a0001c0001t0011g0275 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.800-4314T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097905 | |||||||
chr9:109097910 | T | C | 16 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(13): Show |
16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.800-4319A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097910 | |||||||
chr9:109097989 | T | C | 1 | a0001c0001t0009g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.800-4398A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097989 | |||||||
chr9:109098138 | T | C | 192 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.800-4547A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098138 | |||||||
chr9:109098283 | A | C | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-4692T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098283 | |||||||
chr9:109098517 | C | T | 367 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(364): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.800-4926G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098517 | |||||||
chr9:109098727 | A | G | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.800-5136T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098727 | |||||||
chr9:109098736 | A | C | 1 | a0001c0001t0039g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.800-5145T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098736 | |||||||
chr9:109098840 | G | A | 1 | a0002c0002t0001g0366 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.800-5249C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098840 | |||||||
chr9:109098887 | C | G | 2 | a0001c0005t0003g0010 a0001c0005t0023g0013 |
2 | HG02015.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.800-5296G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098887 | |||||||
chr9:109098917 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-5326G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098917 | |||||||
chr9:109099065 | T | C | 20 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(17): Show |
20 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.800-5474A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099065 | |||||||
chr9:109099097 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-5506G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099097 | |||||||
chr9:109099408 | G | C | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.800-5817C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099408 | |||||||
chr9:109099610 | A | C | 1 | a0001c0001t0009g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.800-6019T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099610 | |||||||
chr9:109099643 | A | C | 1 | a0001c0001t0013g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-6052T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099643 | |||||||
chr9:109100059 | T | C | 1 | a0001c0001t0034g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.799+6449A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100059 | |||||||
chr9:109100464 | T | C | 1 | a0001c0001t0019g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.799+6044A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100464 | |||||||
chr9:109100549 | T | C | 1 | a0002c0002t0021g0367 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.799+5959A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100549 | |||||||
chr9:109100602 | G | A | 1 | a0002c0002t0001g0400 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.799+5906C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100602 | |||||||
chr9:109100720 | C | G | 4 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+5788G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100720 | |||||||
chr9:109100742 | A | G | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5766T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100742 | |||||||
chr9:109100749 | T | C | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5759A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100749 | |||||||
chr9:109101014 | G | A | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5494C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101014 | |||||||
chr9:109101062 | T | C | 2 | a0002c0002t0010g0401 a0002c0002t0010g0402 |
2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.799+5446A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101062 | |||||||
chr9:109101102 | G | A | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.799+5406C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101102 | |||||||
chr9:109101137 | T | C | 57 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(54): Show |
58 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.799+5371A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101137 | |||||||
chr9:109101316 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.799+5192C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101316 | |||||||
chr9:109101368 | A | G | 1 | a0001c0001t0046g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.799+5140T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101368 | |||||||
chr9:109101945 | T | C | 2 | a0001c0001t0013g0229 a0001c0001t0013g0230 |
2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.799+4563A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101945 | |||||||
chr9:109102014 | G | GA | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+4493dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102014 | |||||||
chr9:109102104 | C | T | 1 | a0003c0004t0083g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.799+4404G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102104 | |||||||
chr9:109102456 | A | T | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799+4052T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102456 | |||||||
chr9:109102522 | C | G | 190 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.799+3986G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102522 | |||||||
chr9:109102560 | C | G | 3 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 |
3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.799+3948G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102560 | |||||||
chr9:109102612 | G | GT | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3895dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102612 | |||||||
chr9:109102704 | A | C | 1 | a0001c0001t0003g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.799+3804T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102704 | |||||||
chr9:109102772 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+3736A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102772 | |||||||
chr9:109102913 | G | A | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+3595C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102913 | |||||||
chr9:109102952 | C | A | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3556G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102952 | |||||||
chr9:109103079 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3429A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103079 | |||||||
chr9:109103086 | C | A | 3 | a0001c0001t0027g0199 a0001c0001t0027g0211 a0001c0001t0027g0260 |
3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.799+3422G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103086 | |||||||
chr9:109103257 | C | A | 1 | a0001c0001t0006g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.799+3251G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103257 | |||||||
chr9:109103363 | A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.799+3145T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103363 | |||||||
chr9:109103482 | A | C | 7 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.799+3026T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103482 | |||||||
chr9:109103753 | C | T | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.799+2755G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103753 | |||||||
chr9:109103778 | T | G | 16 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(13): Show |
16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+2730A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103778 | |||||||
chr9:109103861 | G | A | 1 | a0001c0001t0004g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.799+2647C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103861 | |||||||
chr9:109103978 | G | A | 4 | a0001c0001t0004g0082 a0001c0001t0009g0179 a0001c0001t0009g0180 others(1): Show |
4 | NA18946.hp2 NA18973.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2530C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103978 | |||||||
chr9:109104011 | G | C | 4 | a0001c0001t0022g0003 a0001c0001t0022g0004 a0001c0001t0022g0005 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2497C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104011 | |||||||
chr9:109104049 | C | A | 4 | a0002c0002t0001g0368 a0002c0002t0001g0403 a0002c0002t0001g0404 others(1): Show |
4 | HG02165.hp2 NA18747.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+2459G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104049 | |||||||
chr9:109104154 | A | C | 1 | a0002c0002t0001g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.799+2354T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104154 | |||||||
chr9:109104194 | T | C | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+2314A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104194 | |||||||
chr9:109104262 | T | C | 1 | a0003c0004t0031g0331 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.799+2246A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104262 | |||||||
chr9:109104315 | CCTA | C | 4 | a0001c0006t0030g0289 a0001c0006t0030g0290 a0001c0006t0030g0292 others(1): Show |
4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2190_799+2192d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104315 | |||||||
chr9:109104357 | A | C | 30 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(27): Show |
30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.799+2151T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104357 | |||||||
chr9:109104469 | C | T | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+2039G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104469 | |||||||
chr9:109104529 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.799+1979A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104529 | |||||||
chr9:109104614 | G | C | 1 | a0001c0001t0009g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.799+1894C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104614 | |||||||
chr9:109104636 | AT | A | 3 | a0001c0001t0005g0148 a0001c0001t0005g0149 a0001c0001t0005g0155 |
3 | NA18967.hp2 NA18972.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.799+1871delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104636 | |||||||
chr9:109104991 | A | G | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+1517T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104991 | |||||||
chr9:109105010 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+1498A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105010 | |||||||
chr9:109105081 | G | A | 1 | a0002c0002t0010g0355 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.799+1427C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105081 | |||||||
chr9:109105095 | C | A | 19 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.799+1413G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105095 | |||||||
chr9:109105097 | T | C | 1 | a0001c0001t0005g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.799+1411A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105097 | |||||||
chr9:109105159 | A | G | 2 | a0001c0001t0019g0200 a0001c0001t0019g0269 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.799+1349T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105159 | |||||||
chr9:109105275 | C | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 |
3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.799+1233G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105275 | |||||||
chr9:109105327 | G | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.799+1181C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105327 | |||||||
chr9:109105356 | G | T | 6 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(3): Show |
6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.799+1152C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105356 | |||||||
chr9:109105359 | T | C | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799+1149A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105359 | |||||||
chr9:109105464 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+1044T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105464 | |||||||
chr9:109105478 | C | T | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+1030G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105478 | |||||||
chr9:109105496 | C | T | 1 | a0001c0001t0004g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799+1012G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105496 | |||||||
chr9:109105510 | G | T | 1 | a0001c0001t0056g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799+998C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105510 | |||||||
chr9:109105521 | G | A | 31 | a0004c0003t0002g0037 a0004c0003t0002g0038 a0004c0003t0002g0040 others(28): Show |
31 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.799+987C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105521 | |||||||
chr9:109105566 | T | C | 16 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(13): Show |
16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+942A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105566 | |||||||
chr9:109105615 | G | T | 2 | a0001c0001t0012g0115 a0001c0001t0055g0103 |
2 | NA18940.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.799+893C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105615 | |||||||
chr9:109105768 | T | C | 1 | a0004c0003t0002g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.799+740A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105768 | |||||||
chr9:109106004 | C | T | 26 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0102 others(23): Show |
26 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(23): Show |
intron_variant | MODIFIER | c.799+504G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106004 | |||||||
chr9:109106018 | T | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+490A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106018 | |||||||
chr9:109106032 | A | G | 2 | a0003c0004t0017g0324 a0003c0004t0017g0325 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.799+476T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106032 | |||||||
chr9:109106064 | G | A | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+444C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106064 | |||||||
chr9:109106092 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.799+416A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106092 | |||||||
chr9:109106225 | A | AAAAAATA others(22): Show |
86 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(83): Show |
87 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.799+254_799+282dup others(29): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106225 | |||||||
chr9:109106225 | A | AAAAAATA others(51): Show |
1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.799+282_799+283ins others(58): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106225 | |||||||
chr9:109106403 | T | C | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.799+105A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106403 | |||||||
chr9:109106418 | A | G | 28 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+90T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106418 | |||||||
chr9:109106462 | C | G | 4 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+46G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106462 | |||||||
chr9:109106464 | A | C | 1 | a0003c0004t0031g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.799+44T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106464 | |||||||
chr9:109106497 | C | T | 16 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(13): Show |
16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+11G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106497 | |||||||
chr9:109106657 | A | G | 2 | a0001c0001t0005g0101 a0001c0001t0076g0083 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.698-48T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106657 | |||||||
chr9:109106736 | C | CA | 5 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(2): Show |
6 | HG01433.hp1 HG01496.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.698-128dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106736 | |||||||
chr9:109106837 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-228A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106837 | |||||||
chr9:109106911 | G | T | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-302C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106911 | |||||||
chr9:109106944 | C | G | 3 | a0001c0001t0012g0026 a0001c0001t0012g0027 a0001c0001t0012g0028 |
3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.698-335G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106944 | |||||||
chr9:109106952 | G | A | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-343C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106952 | |||||||
chr9:109107013 | CTT | C | 35 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(32): Show |
35 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.698-406_698-405del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107013 | |||||||
chr9:109107180 | G | A | 62 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(59): Show |
62 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.698-571C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107180 | |||||||
chr9:109107242 | A | T | 1 | a0001c0001t0043g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.698-633T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107242 | |||||||
chr9:109107243 | A | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.698-634T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107243 | |||||||
chr9:109107331 | G | A | 19 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.698-722C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107331 | |||||||
chr9:109107398 | CA | C | 38 | a0001c0001t0003g0264 a0001c0001t0007g0030 a0001c0001t0065g0029 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.698-790delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107398 | |||||||
chr9:109107417 | A | AT | 49 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0129 others(46): Show |
49 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.698-809_698-808ins others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107417 | |||||||
chr9:109107417 | A | T | 319 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(316): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.698-808T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107417 | |||||||
chr9:109107418 | G | A | 1 | a0002c0002t0021g0405 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.698-809C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107418 | |||||||
chr9:109107430 | C | T | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.698-821G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107430 | |||||||
chr9:109107470 | C | T | 5 | a0001c0001t0004g0117 a0001c0001t0006g0084 a0001c0001t0006g0085 others(2): Show |
5 | HG00558.hp2 HG02027.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-861G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107470 | |||||||
chr9:109107629 | C | T | 19 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(16): Show |
19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.697+824G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107629 | |||||||
chr9:109107654 | T | C | 30 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(27): Show |
30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.697+799A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107654 | |||||||
chr9:109107675 | T | C | 1 | a0001c0001t0040g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.697+778A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107675 | |||||||
chr9:109107801 | C | T | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.697+652G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107801 | |||||||
chr9:109107805 | G | A | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.697+648C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107805 | |||||||
chr9:109107988 | C | G | 1 | a0001c0006t0011g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.697+465G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107988 | |||||||
chr9:109108121 | G | A | 6 | a0003c0004t0007g0315 a0003c0004t0007g0316 a0003c0004t0007g0317 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+332C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108121 | |||||||
chr9:109108246 | T | C | 12 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.697+207A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108246 | |||||||
chr9:109108420 | T | TA | 44 | a0001c0001t0007g0030 a0001c0001t0008g0161 a0001c0001t0008g0162 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.697+32dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | |||||||
chr9:109108420 | T | TAAA | 34 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0129 others(31): Show |
34 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.697+30_697+32dupTT others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | |||||||
chr9:109108420 | TA | T | 22 | a0001c0001t0003g0232 a0001c0001t0003g0249 a0001c0001t0004g0193 others(19): Show |
22 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.697+32delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | |||||||
chr9:109108441 | G | A | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.697+12C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108441 | |||||||
chr9:109108614 | A | C | 2 | a0001c0001t0004g0274 a0001c0001t0013g0273 |
2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.580-44T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108614 | |||||||
chr9:109108730 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580-160C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108730 | |||||||
chr9:109108898 | T | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-328A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108898 | |||||||
chr9:109109061 | A | T | 176 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.580-491T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109061 | |||||||
chr9:109109235 | G | C | 62 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(59): Show |
62 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.580-665C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109235 | |||||||
chr9:109109276 | C | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-706G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109276 | |||||||
chr9:109109280 | T | A | 1 | a0008c0019t0001g0406 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.580-710A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109280 | |||||||
chr9:109109386 | A | C | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-816T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109386 | |||||||
chr9:109109436 | C | CA | 44 | a0001c0001t0007g0030 a0001c0001t0008g0160 a0001c0001t0008g0161 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.580-867dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109436 | |||||||
chr9:109109504 | A | C | 3 | a0003c0004t0007g0312 a0003c0004t0007g0313 a0003c0004t0007g0343 |
3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.580-934T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109504 | |||||||
chr9:109109523 | A | G | 1 | a0001c0001t0014g0233 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.580-953T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109523 | |||||||
chr9:109109584 | T | C | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.580-1014A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109584 | |||||||
chr9:109109585 | C | T | 30 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(27): Show |
30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.580-1015G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109585 | |||||||
chr9:109109817 | A | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(49): Show |
53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-1247T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109817 | |||||||
chr9:109109914 | A | T | 1 | a0001c0001t0054g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-1344T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109914 | |||||||
chr9:109110125 | G | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580-1555C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110125 | |||||||
chr9:109110277 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-1707G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110277 | |||||||
chr9:109110465 | A | G | 4 | a0002c0002t0001g0361 a0002c0002t0001g0362 a0002c0002t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1895T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110465 | |||||||
chr9:109110529 | A | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(49): Show |
53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-1959T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110529 | |||||||
chr9:109110564 | T | C | 50 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(47): Show |
50 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.580-1994A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110564 | |||||||
chr9:109110570 | T | TA | 245 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.580-2001dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110570 | |||||||
chr9:109110717 | G | A | 7 | a0001c0007t0004g0297 a0001c0007t0004g0298 a0001c0007t0004g0299 others(4): Show |
7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-2147C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110717 | |||||||
chr9:109110916 | A | C | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-2346T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110916 | |||||||
chr9:109110947 | A | G | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-2377T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110947 | |||||||
chr9:109111049 | TA | T | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.580-2480delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111049 | |||||||
chr9:109111058 | T | C | 1 | a0001c0015t0004g0268 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.580-2488A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111058 | |||||||
chr9:109111098 | A | G | 2 | a0001c0001t0009g0102 a0001c0016t0012g0293 |
2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.580-2528T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111098 | |||||||
chr9:109111552 | GTTTAAAA others(7): Show |
G | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.580-2996_580-2983d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111552 | |||||||
chr9:109111582 | C | T | 3 | a0002c0002t0001g0359 a0002c0002t0047g0358 a0002c0002t0047g0360 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.580-3012G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111582 | |||||||
chr9:109111694 | T | A | 2 | a0001c0001t0037g0114 a0001c0001t0037g0116 |
2 | NA18943.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.580-3124A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111694 | |||||||
chr9:109111829 | C | CA | 29 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-3260dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111829 | |||||||
chr9:109111928 | T | C | 1 | a0001c0001t0075g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.580-3358A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111928 | |||||||
chr9:109111934 | A | G | 31 | a0001c0001t0011g0189 a0001c0001t0011g0275 a0001c0001t0011g0277 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-3364T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111934 | |||||||
chr9:109112113 | C | T | 1 | a0002c0002t0001g0357 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.580-3543G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112113 | |||||||
chr9:109112296 | T | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-3726A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112296 | |||||||
chr9:109112338 | C | G | 1 | a0001c0001t0020g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.580-3768G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112338 | |||||||
chr9:109112466 | A | G | 176 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.580-3896T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112466 | |||||||
chr9:109112473 | G | A | 1 | a0001c0001t0006g0099 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.580-3903C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112473 | |||||||
chr9:109112502 | T | C | 29 | a0001c0001t0004g0082 a0001c0001t0004g0182 a0001c0001t0009g0077 others(26): Show |
29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.580-3932A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112502 | |||||||
chr9:109112541 | C | CA | 46 | a0001c0001t0004g0231 a0001c0001t0007g0030 a0001c0001t0008g0160 others(43): Show |
46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.580-3972dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112541 | |||||||
chr9:109112648 | T | C | 1 | a0003c0004t0081g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-4078A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112648 | |||||||
chr9:109112675 | A | C | 1 | a0001c0001t0039g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.580-4105T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112675 | |||||||
chr9:109112781 | G | A | 1 | a0001c0001t0045g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.580-4211C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112781 | |||||||
chr9:109112800 | G | A | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580-4230C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112800 | |||||||
chr9:109112805 | C | T | 113 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(110): Show |
114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.580-4235G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112805 | |||||||
chr9:109112935 | G | A | 1 | a0002c0002t0001g0407 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.580-4365C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112935 | |||||||
chr9:109112938 | T | C | 2 | a0001c0001t0005g0157 a0001c0001t0013g0124 |
2 | HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.580-4368A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112938 | |||||||
chr9:109112939 | G | A | 2 | a0001c0001t0035g0271 a0001c0001t0035g0272 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-4369C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112939 | |||||||
chr9:109112968 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-4398G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112968 | |||||||
chr9:109113043 | T | C | 1 | a0001c0001t0012g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.580-4473A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113043 | |||||||
chr9:109113130 | C | T | 3 | a0001c0006t0041g0286 a0001c0006t0041g0287 a0001c0006t0061g0288 |
3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.580-4560G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113130 | |||||||
chr9:109113183 | G | A | 189 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.580-4613C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113183 | |||||||
chr9:109113312 | C | T | 16 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(13): Show |
16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-4742G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113312 | |||||||
chr9:109113391 | G | C | 1 | a0001c0001t0005g0125 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.580-4821C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113391 | |||||||
chr9:109113760 | T | C | 1 | a0001c0001t0037g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.580-5190A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113760 | |||||||
chr9:109113918 | C | T | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.580-5348G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113918 | |||||||
chr9:109113995 | G | C | 1 | a0001c0001t0040g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+5340C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113995 | |||||||
chr9:109114024 | C | T | 28 | a0001c0001t0004g0117 a0001c0001t0006g0078 a0001c0001t0006g0080 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+5311G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114024 | |||||||
chr9:109114037 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.579+5298A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114037 | |||||||
chr9:109114076 | CCAAAA | C | 25 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(22): Show |
25 | HG00558.hp1 HG00735.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+5254_579+5258d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114076 | |||||||
chr9:109114243 | A | G | 76 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.579+5092T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114243 | |||||||
chr9:109114259 | T | C | 9 | a0003c0008t0016g0304 a0003c0008t0016g0305 a0003c0008t0016g0308 others(6): Show |
9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+5076A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114259 | |||||||
chr9:109114491 | AGAG | A | 8 | a0001c0001t0008g0166 a0001c0001t0008g0167 a0001c0001t0008g0168 others(5): Show |
8 | HG00639.hp2 HG02572.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+4841_579+4843d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114491 | |||||||
chr9:109114543 | A | C | 21 | a0001c0001t0003g0215 a0001c0001t0003g0220 a0001c0001t0003g0261 others(18): Show |
21 | HG00558.hp1 HG02040.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+4792T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114543 | |||||||
chr9:109114558 | G | C | 3 | a0004c0003t0002g0073 a0004c0003t0002g0074 a0004c0003t0002g0075 |
3 | HG00408.hp1 NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.579+4777C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114558 | |||||||
chr9:109114741 | G | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+4594C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114741 | |||||||
chr9:109114744 | G | A | 31 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0001c0009t0017g0002 others(28): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+4591C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114744 | |||||||
chr9:109114852 | AT | A | 171 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.579+4482delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114852 | |||||||
chr9:109115134 | G | A | 1 | a0003c0008t0067g0306 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.579+4201C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115134 | |||||||
chr9:109115148 | A | C | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+4187T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115148 | |||||||
chr9:109115176 | G | A | 17 | a0001c0001t0008g0160 a0001c0001t0008g0161 a0001c0001t0008g0162 others(14): Show |
17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.579+4159C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115176 | |||||||
chr9:109115203 | A | G | 1 | a0001c0001t0076g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+4132T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115203 | |||||||
chr9:109115228 | T | C | 2 | a0001c0001t0004g0182 a0001c0001t0036g0181 |
2 | NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.579+4107A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115228 | |||||||
chr9:109115318 | T | C | 2 | a0003c0004t0044g0319 a0003c0004t0044g0320 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.579+4017A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115318 | |||||||
chr9:109115357 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0076 |
2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.579+3978C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115357 | |||||||
chr9:109115431 | A | C | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.579+3904T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115431 | |||||||
chr9:109115522 | C | CT | 50 | a0001c0001t0003g0201 a0001c0001t0003g0202 a0001c0001t0003g0203 others(47): Show |
51 | HG00438.hp2 HG00544.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+3812dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115522 | C | CTT | 6 | a0001c0001t0003g0263 a0001c0006t0011g0280 a0002c0002t0018g0350 others(3): Show |
6 | HG00621.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+3811_579+3812d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115522 | C | CTTT | 17 | a0001c0001t0065g0029 a0003c0004t0007g0312 a0003c0004t0007g0315 others(14): Show |
17 | HG02451.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+3810_579+3812d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115522 | C | CTTTT | 7 | a0001c0001t0007g0030 a0003c0004t0007g0326 a0003c0004t0007g0329 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+3809_579+3812d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115522 | CT | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0042 others(140): Show |
144 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.579+3812delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115522 | CTT | C | 8 | a0001c0001t0005g0152 a0001c0001t0005g0153 a0001c0001t0005g0154 others(5): Show |
8 | HG01168.hp2 HG01256.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3811_579+3812d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | |||||||
chr9:109115593 | C | T | 5 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0265 others(2): Show |
5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+3742G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115593 | |||||||
chr9:109115594 | G | A | 1 | a0001c0001t0004g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.579+3741C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115594 | |||||||
chr9:109115606 | T | C | 27 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0007g0312 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+3729A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115606 | |||||||
chr9:109115683 | T | C | 302 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579+3652A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115683 | |||||||
chr9:109115712 | T | C | 2 | a0003c0012t0063g0022 a0003c0018t0066g0307 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+3623A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115712 | |||||||
chr9:109115750 | G | A | 1 | a0001c0001t0034g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+3585C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115750 | |||||||
chr9:109115762 | T | C | 2 | a0001c0009t0017g0002 a0001c0009t0017g0302 |
3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.579+3573A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115762 | |||||||
chr9:109115782 | G | A | 1 | a0002c0002t0001g0408 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.579+3553C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115782 | |||||||
chr9:109115798 | G | A | 2 | a0001c0001t0057g0118 a0001c0001t0058g0119 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.579+3537C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115798 | |||||||
chr9:109115892 | G | T | 53 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(50): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.579+3443C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115892 | |||||||
chr9:109116058 | A | G | 1 | a0001c0013t0064g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.579+3277T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116058 | |||||||
chr9:109116244 | T | C | 5 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0265 others(2): Show |
5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+3091A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116244 | |||||||
chr9:109116498 | T | C | 1 | a0001c0015t0004g0268 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.579+2837A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116498 | |||||||
chr9:109116540 | C | CT | 32 | a0001c0001t0002g0032 a0001c0001t0065g0029 a0001c0006t0011g0280 others(29): Show |
32 | HG00738.hp2 HG01109.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+2794dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116540 | |||||||
chr9:109116602 | A | T | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+2733T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116602 | |||||||
chr9:109116676 | G | A | 77 | a0001c0001t0019g0269 a0002c0002t0001g0345 a0002c0002t0001g0346 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.579+2659C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116676 | |||||||
chr9:109117043 | T | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(111): Show |
115 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.579+2292A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117043 | |||||||
chr9:109117069 | C | T | 2 | a0001c0001t0045g0174 a0001c0001t0045g0176 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.579+2266G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117069 | |||||||
chr9:109117117 | G | T | 1 | a0001c0005t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.579+2218C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117117 | |||||||
chr9:109117118 | T | G | 81 | a0001c0001t0045g0174 a0001c0009t0017g0002 a0001c0009t0017g0302 others(78): Show |
82 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.579+2217A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117118 | |||||||
chr9:109117133 | G | T | 1 | a0001c0001t0014g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.579+2202C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117133 | |||||||
chr9:109117158 | G | A | 32 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0002g0321 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+2177C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117158 | |||||||
chr9:109117160 | A | C | 1 | a0001c0001t0034g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.579+2175T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117160 | |||||||
chr9:109117258 | C | T | 1 | a0001c0001t0054g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.579+2077G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117258 | |||||||
chr9:109117276 | A | AT | 120 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(117): Show |
121 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.579+2058dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117276 | |||||||
chr9:109117510 | C | G | 1 | a0001c0001t0006g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.579+1825G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117510 | |||||||
chr9:109117679 | G | A | 2 | a0003c0008t0016g0309 a0003c0008t0016g0310 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.579+1656C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117679 | |||||||
chr9:109117746 | T | C | 115 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(112): Show |
117 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.579+1589A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117746 | |||||||
chr9:109117894 | T | A | 4 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0004t0081g0342 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1441A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117894 | |||||||
chr9:109117942 | G | A | 3 | a0001c0009t0017g0002 a0001c0009t0017g0302 a0003c0017t0082g0311 |
4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1393C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117942 | |||||||
chr9:109118072 | A | T | 38 | a0001c0001t0005g0121 a0001c0001t0005g0123 a0001c0001t0005g0125 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.579+1263T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118072 | |||||||
chr9:109118128 | G | A | 1 | a0004c0003t0029g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.579+1207C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118128 | |||||||
chr9:109118168 | C | T | 3 | a0003c0004t0007g0312 a0003c0004t0007g0313 a0003c0004t0007g0343 |
3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.579+1167G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118168 | |||||||
chr9:109118186 | C | T | 6 | a0001c0006t0011g0280 a0001c0006t0011g0281 a0001c0006t0011g0282 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+1149G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118186 | |||||||
chr9:109118373 | G | T | 1 | a0001c0001t0040g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+962C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118373 | |||||||
chr9:109118385 | T | C | 5 | a0001c0001t0048g0006 a0001c0006t0030g0289 a0001c0006t0030g0290 others(2): Show |
5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+950A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118385 | |||||||
chr9:109118413 | T | C | 113 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(110): Show |
114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.579+922A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118413 | |||||||
chr9:109118433 | A | G | 111 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.579+902T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118433 | |||||||
chr9:109118436 | T | C | 1 | a0001c0001t0006g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.579+899A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118436 | |||||||
chr9:109118443 | G | GT | 6 | a0002c0002t0001g0345 a0002c0002t0001g0346 a0002c0002t0001g0347 others(3): Show |
6 | HG01257.hp1 HG01358.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+891dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118443 | |||||||
chr9:109118456 | T | C | 302 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579+879A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118456 | |||||||
chr9:109118529 | T | C | 1 | a0003c0004t0007g0343 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.579+806A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118529 | |||||||
chr9:109118558 | G | A | 9 | a0002c0002t0001g0411 a0002c0002t0001g0412 a0002c0002t0001g0413 others(6): Show |
9 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+777C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118558 | |||||||
chr9:109118620 | G | A | 1 | a0003c0017t0082g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.579+715C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118620 | |||||||
chr9:109118629 | T | C | 1 | a0001c0001t0045g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.579+706A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118629 | |||||||
chr9:109118990 | C | T | 3 | a0001c0005t0003g0007 a0001c0005t0003g0008 a0001c0005t0003g0009 |
3 | NA19011.hp1 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.579+345G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118990 | |||||||
chr9:109119018 | C | A | 6 | a0001c0001t0004g0182 a0001c0001t0009g0179 a0001c0001t0009g0180 others(3): Show |
6 | HG04204.hp2 NA18946.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+317G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119018 | |||||||
chr9:109119070 | A | G | 43 | a0001c0001t0007g0030 a0001c0001t0065g0029 a0003c0004t0002g0321 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.579+265T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119070 | |||||||
chr9:109119071 | T | C | 2 | a0001c0001t0035g0271 a0001c0001t0035g0272 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.579+264A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119071 | |||||||
chr9:109119089 | T | A | 4 | a0001c0001t0011g0275 a0001c0001t0011g0277 a0001c0001t0011g0278 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+246A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119089 | |||||||
chr9:109119117 | G | A | 2 | a0001c0001t0004g0274 a0001c0001t0013g0273 |
2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.579+218C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119117 | |||||||
chr9:109119120 | A | G | 302 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0034 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579+215T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119120 | |||||||
chr9:109119166 | G | C | 5 | a0001c0001t0011g0275 a0001c0001t0011g0277 a0001c0001t0011g0278 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+169C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119166 | |||||||
chr9:109119275 | T | C | 1 | a0001c0001t0020g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.579+60A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119275 | |||||||
chr9:109119289 | G | T | 3 | a0001c0001t0012g0026 a0001c0001t0012g0027 a0001c0001t0012g0028 |
3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.579+46C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119289 |