Item | Value |
---|---|
geneid | 201931 |
ensemblid | ENSG00000170088.14 |
hgncid | 26775 |
symbol | TMEM192 |
name | transmembrane protein 192 |
refseq_nuc | NM_001100389.2 |
refseq_prot | NP_001093859.1 |
ensembl_nuc | ENST00000306480.11 |
ensembl_prot | ENSP00000305069.4 |
mane_status | MANE Select |
chr | chr4 |
start | 165070608 |
end | 165112860 |
strand | - |
ver | v1.2 |
region | chr4:165070608-165112860 |
region5000 | chr4:165065608-165117860 |
regionname0 | TMEM192_chr4_165070608_165112860 |
regionname5000 | TMEM192_chr4_165065608_165117860 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 813 | 194 | 36 | 48 | 72 | 10 | 26 | TMEM192_chr4_165065608_165117860 | TMEM192 | ATGGC others(808): Show |
chr4 | 165065608 | 165117860 | ||
a0001c0002 | 0/0 | 813 | 136 | 56 | 10 | 58 | 2 | 10 | TMEM192_chr4_165065608_165117860 | TMEM192 | ATGGC others(808): Show |
chr4 | 165065608 | 165117860 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9954 | 41 | 0 | 10 | 25 | 1 | 5 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0002 | 0/0 | 9956 | 25 | 1 | 15 | 5 | 2 | 2 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0003 | 0/0 | 9957 | 5 | 0 | 1 | 4 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0004 | 0/0 | 9956 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0005 | 0/0 | 9954 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0006 | 0/0 | 9954 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0008 | 0/0 | 9954 | 5 | 1 | 2 | 0 | 2 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0009 | 0/0 | 9954 | 5 | 1 | 2 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0011 | 0/0 | 9956 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0012 | 0/0 | 9952 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0013 | 0/1 | 9954 | 3 | 0 | 1 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0014 | 0/0 | 9950 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9945): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0015 | 0/0 | 9955 | 4 | 1 | 2 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0016 | 0/0 | 9956 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0018 | 0/0 | 9955 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0019 | 0/0 | 9954 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0020 | 0/0 | 9955 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0021 | 0/0 | 9958 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0022 | 0/0 | 9958 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0025 | 0/0 | 9954 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0026 | 0/0 | 9954 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0027 | 0/0 | 9957 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0028 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0029 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0030 | 0/0 | 9956 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0033 | 0/0 | 9954 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0034 | 0/0 | 9954 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0035 | 0/0 | 9954 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0036 | 0/0 | 9955 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0037 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0038 | 0/0 | 9954 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0039 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0040 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0041 | 0/0 | 9954 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0042 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0043 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0046 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0052 | 0/0 | 9956 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0053 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0056 | 0/0 | 9956 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0057 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0064 | 0/0 | 9956 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0065 | 0/0 | 9956 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0066 | 0/0 | 9956 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0069 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0071 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0072 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0074 | 0/0 | 9956 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0075 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0077 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0078 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0080 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0081 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0083 | 0/0 | 9955 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0084 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0085 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0086 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0087 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0088 | 0/0 | 9956 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0089 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0090 | 0/0 | 9953 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0092 | 0/0 | 9954 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0093 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0094 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0095 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0096 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0098 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0099 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0100 | 0/0 | 9955 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0101 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0102 | 0/0 | 9955 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0105 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0106 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0107 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0112 | 1/0 | 9953 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0120 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0122 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0123 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0125 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0001t0130 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0001 | 0/0 | 9954 | 14 | 0 | 0 | 14 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0002 | 0/0 | 9956 | 19 | 5 | 4 | 9 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0003 | 0/0 | 9957 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0004 | 0/0 | 9956 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0006 | 0/0 | 9954 | 5 | 2 | 0 | 0 | 2 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0007 | 0/0 | 9955 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0010 | 0/0 | 9956 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0011 | 0/0 | 9956 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0013 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0014 | 0/0 | 9950 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9945): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0016 | 0/0 | 9956 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0017 | 0/0 | 9956 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0020 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0022 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0023 | 0/0 | 9951 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9946): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0024 | 0/0 | 9954 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0028 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0029 | 0/0 | 9954 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0031 | 0/0 | 9953 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0032 | 0/0 | 9958 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0037 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0039 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0040 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0042 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0043 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0044 | 0/0 | 9955 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0045 | 0/0 | 9951 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9946): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0046 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0047 | 0/0 | 9954 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0048 | 0/0 | 9949 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9944): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0049 | 0/0 | 9952 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0050 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0051 | 0/0 | 9955 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0054 | 0/0 | 9956 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0055 | 0/0 | 9956 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0058 | 0/0 | 9957 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0059 | 0/0 | 9956 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0060 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0061 | 0/0 | 9956 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0062 | 0/0 | 9956 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0063 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0067 | 0/0 | 9957 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9952): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0068 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9953): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0070 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0073 | 0/0 | 9956 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0076 | 0/0 | 9955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0079 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0082 | 0/0 | 9955 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0091 | 0/0 | 9952 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0097 | 0/0 | 9959 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9954): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0103 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0104 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0108 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0109 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0110 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0111 | 0/0 | 9950 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9945): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0113 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0114 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0115 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0116 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0117 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9948): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0118 | 0/0 | 9959 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9954): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0119 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0121 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9950): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0124 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0126 | 0/0 | 9950 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9945): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0127 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9949): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0128 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0129 | 0/0 | 9952 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9947): Show |
chr4 | 165065608 | 165117860 |
a0001c0002t0131 | 0/0 | 9956 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | AGAAG others(9951): Show |
chr4 | 165065608 | 165117860 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0008g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0009g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0011g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0012g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0012g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0013g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0013g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0013g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0014g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0015g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0016g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0018g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0019g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0019g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0020g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0021g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0021g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0025g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0026g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0026g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0027g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0027g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0028g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0029g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0030g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0030g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0033g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0033g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0034g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0034g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0035g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0035g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0036g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0036g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0037g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0038g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0038g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0039g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0040g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0041g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0041g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0042g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0043g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0046g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0052g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0053g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0056g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0057g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0064g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0065g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0066g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0069g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0071g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0072g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0074g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0075g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0077g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0078g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0080g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0081g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0083g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0084g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0085g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0086g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0087g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0088g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0089g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0090g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0092g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0093g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0094g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0095g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0096g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0098g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0099g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0100g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0101g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0102g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0105g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0106g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0107g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0112g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0120g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0122g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0123g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0125g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0001t0130g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0013g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0016g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0017g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0017g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0017g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0020g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0022g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0023g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0023g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0024g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0024g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0024g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0028g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0029g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0031g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0031g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0032g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0032g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0037g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0039g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0040g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0042g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0043g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0044g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0044g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0045g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0045g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0046g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0047g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0047g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0048g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0048g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0049g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0049g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0050g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0051g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0054g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0055g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0058g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0059g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0060g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0061g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0062g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0063g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0067g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0068g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0070g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0073g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0076g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0079g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0082g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0091g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0097g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0103g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0104g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0108g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0109g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0110g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0111g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0113g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0114g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0115g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0116g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0117g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0118g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0119g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0121g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0124g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0126g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0127g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0128g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0129g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
a0001c0002t0131g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0066 | g0240 | EUR | GBR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00099 | hp2 | a0001 | c0001 | t0078 | g0126 | EUR | GBR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00140 | hp2 | a0001 | c0001 | t0013 | g0116 | EUR | GBR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0121 | EUR | FIN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00323 | hp2 | a0001 | c0002 | t0006 | g0192 | EUR | FIN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00609 | hp2 | a0001 | c0001 | t0016 | g0288 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00621 | hp2 | a0001 | c0002 | t0058 | g0229 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00673 | hp1 | a0001 | c0002 | t0014 | g0047 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00673 | hp2 | a0001 | c0001 | t0014 | g0112 | EAS | CHS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00735 | hp2 | a0001 | c0001 | t0012 | g0105 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG00741 | hp2 | a0001 | c0002 | t0029 | g0220 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0223 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0309 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01081 | hp2 | a0001 | c0001 | t0046 | g0025 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01109 | hp2 | a0001 | c0001 | t0123 | g0058 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01192 | hp1 | a0001 | c0001 | t0065 | g0157 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01243 | hp1 | a0001 | c0001 | t0092 | g0102 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01255 | hp1 | a0001 | c0002 | t0073 | g0315 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01261 | hp1 | a0001 | c0001 | t0009 | g0232 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01358 | hp1 | a0001 | c0001 | t0012 | g0104 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01361 | hp1 | a0001 | c0001 | t0102 | g0310 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01496 | hp1 | a0001 | c0001 | t0037 | g0064 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0093 | EUR | IBS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01516 | hp2 | a0001 | c0001 | t0085 | g0095 | EUR | IBS | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01884 | hp2 | a0001 | c0002 | t0048 | g0307 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01891 | hp1 | a0001 | c0002 | t0023 | g0252 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01934 | hp2 | a0001 | c0001 | t0015 | g0100 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01943 | hp2 | a0001 | c0001 | t0009 | g0314 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01952 | hp2 | a0001 | c0001 | t0030 | g0123 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01975 | hp1 | a0001 | c0001 | t0057 | g0131 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01978 | hp1 | a0001 | c0001 | t0015 | g0138 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01978 | hp2 | a0001 | c0001 | t0030 | g0269 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01993 | hp1 | a0001 | c0001 | t0012 | g0193 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02004 | hp1 | a0001 | c0001 | t0013 | g0111 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02004 | hp2 | a0001 | c0001 | t0056 | g0280 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02015 | hp2 | a0001 | c0001 | t0011 | g0242 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02027 | hp2 | a0001 | c0001 | t0041 | g0115 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02040 | hp1 | a0001 | c0002 | t0043 | g0196 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02055 | hp1 | a0001 | c0002 | t0007 | g0171 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02055 | hp2 | a0001 | c0002 | t0007 | g0015 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02056 | hp1 | a0001 | c0001 | t0028 | g0158 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02056 | hp2 | a0001 | c0001 | t0015 | g0087 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02074 | hp2 | a0001 | c0001 | t0029 | g0096 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02083 | hp1 | a0001 | c0002 | t0079 | g0207 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02083 | hp2 | a0001 | c0002 | t0016 | g0228 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02129 | hp1 | a0001 | c0001 | t0011 | g0268 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02132 | hp1 | a0001 | c0001 | t0080 | g0153 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02135 | hp1 | a0001 | c0002 | t0091 | g0150 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0065 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02145 | hp2 | a0001 | c0001 | t0020 | g0059 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02257 | hp2 | a0001 | c0001 | t0122 | g0021 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02258 | hp1 | a0001 | c0002 | t0118 | g0251 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02258 | hp2 | a0001 | c0002 | t0113 | g0182 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0130 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0200 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02280 | hp2 | a0001 | c0002 | t0007 | g0003 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02300 | hp2 | a0001 | c0002 | t0017 | g0227 | AMR | PEL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02451 | hp1 | a0001 | c0001 | t0021 | g0057 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02451 | hp2 | a0001 | c0002 | t0116 | g0019 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02523 | hp1 | a0001 | c0001 | t0041 | g0028 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02523 | hp2 | a0001 | c0002 | t0063 | g0029 | EAS | KHV | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02572 | hp1 | a0001 | c0002 | t0044 | g0257 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02572 | hp2 | a0001 | c0001 | t0106 | g0263 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02602 | hp1 | a0001 | c0001 | t0035 | g0285 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02615 | hp1 | a0001 | c0002 | t0007 | g0016 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02615 | hp2 | a0001 | c0002 | t0047 | g0306 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02622 | hp2 | a0001 | c0002 | t0031 | g0238 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02630 | hp1 | a0001 | c0001 | t0105 | g0262 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0313 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02647 | hp2 | a0001 | c0002 | t0031 | g0201 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02683 | hp1 | a0001 | c0002 | t0050 | g0191 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02698 | hp1 | a0001 | c0001 | t0083 | g0312 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0101 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02723 | hp1 | a0001 | c0002 | t0059 | g0218 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02723 | hp2 | a0001 | c0001 | t0099 | g0055 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02738 | hp1 | a0001 | c0002 | t0131 | g0311 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02738 | hp2 | a0001 | c0001 | t0052 | g0275 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02818 | hp1 | a0001 | c0001 | t0039 | g0165 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02886 | hp1 | a0001 | c0002 | t0044 | g0181 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02886 | hp2 | a0001 | c0001 | t0043 | g0022 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02895 | hp1 | a0001 | c0001 | t0040 | g0052 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02895 | hp2 | a0001 | c0002 | t0119 | g0026 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02896 | hp1 | a0001 | c0002 | t0022 | g0062 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02896 | hp2 | a0001 | c0001 | t0096 | g0176 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02897 | hp1 | a0001 | c0002 | t0040 | g0061 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02897 | hp2 | a0001 | c0001 | t0022 | g0056 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02922 | hp1 | a0001 | c0002 | t0045 | g0255 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02922 | hp2 | a0001 | c0002 | t0006 | g0180 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02970 | hp1 | a0001 | c0001 | t0020 | g0060 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02970 | hp2 | a0001 | c0002 | t0047 | g0256 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02976 | hp2 | a0001 | c0001 | t0098 | g0244 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03041 | hp1 | a0001 | c0002 | t0054 | g0080 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03041 | hp2 | a0001 | c0002 | t0097 | g0249 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03130 | hp1 | a0001 | c0001 | t0022 | g0023 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03130 | hp2 | a0001 | c0002 | t0126 | g0086 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03139 | hp1 | a0001 | c0002 | t0061 | g0082 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03139 | hp2 | a0001 | c0002 | t0124 | g0024 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03195 | hp1 | a0001 | c0001 | t0086 | g0113 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03195 | hp2 | a0001 | c0001 | t0120 | g0120 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03209 | hp1 | a0001 | c0001 | t0021 | g0053 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03209 | hp2 | a0001 | c0002 | t0049 | g0264 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03225 | hp1 | a0001 | c0001 | t0038 | g0164 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03225 | hp2 | a0001 | c0002 | t0049 | g0267 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03239 | hp2 | a0001 | c0001 | t0081 | g0161 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03453 | hp1 | a0001 | c0001 | t0125 | g0079 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03453 | hp2 | a0001 | c0002 | t0032 | g0204 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03486 | hp1 | a0001 | c0002 | t0129 | g0266 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03486 | hp2 | a0001 | c0002 | t0023 | g0248 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03490 | hp1 | a0001 | c0001 | t0027 | g0289 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03490 | hp2 | a0001 | c0001 | t0034 | g0119 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03492 | hp1 | a0001 | c0001 | t0034 | g0108 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03516 | hp2 | a0001 | c0002 | t0110 | g0185 | AFR | ESN | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03540 | hp1 | a0001 | c0001 | t0094 | g0247 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | GWD | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03579 | hp1 | a0001 | c0001 | t0021 | g0054 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03579 | hp2 | a0001 | c0002 | t0007 | g0003 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03654 | hp1 | a0001 | c0001 | t0069 | g0068 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03654 | hp2 | a0001 | c0002 | t0051 | g0197 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03688 | hp1 | a0001 | c0001 | t0072 | g0152 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03688 | hp2 | a0001 | c0001 | t0130 | g0154 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03704 | hp1 | a0001 | c0002 | t0055 | g0198 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03704 | hp2 | a0001 | c0001 | t0035 | g0146 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03710 | hp1 | a0001 | c0002 | t0013 | g0195 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03710 | hp2 | a0001 | c0001 | t0090 | g0063 | SAS | PJL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03831 | hp1 | a0001 | c0001 | t0033 | g0129 | SAS | BEB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03831 | hp2 | a0001 | c0001 | t0071 | g0128 | SAS | BEB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04115 | hp1 | a0001 | c0001 | t0036 | g0162 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0188 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04184 | hp1 | a0001 | c0002 | t0082 | g0194 | SAS | BEB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04184 | hp2 | a0001 | c0001 | t0101 | g0099 | SAS | BEB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04199 | hp2 | a0001 | c0001 | t0027 | g0281 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04228 | hp1 | a0001 | c0002 | t0108 | g0210 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG04228 | hp2 | a0001 | c0001 | t0089 | g0071 | SAS | STU | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18522 | hp1 | a0001 | c0002 | t0039 | g0254 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18612 | hp2 | a0001 | c0001 | t0018 | g0169 | EAS | CHB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18906 | hp1 | a0001 | c0002 | t0111 | g0172 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18906 | hp2 | a0001 | c0001 | t0095 | g0178 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18941 | hp1 | a0001 | c0002 | t0017 | g0225 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18941 | hp2 | a0001 | c0001 | t0009 | g0231 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18947 | hp1 | a0001 | c0001 | t0009 | g0233 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18949 | hp2 | a0001 | c0002 | t0037 | g0032 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18950 | hp1 | a0001 | c0002 | t0016 | g0213 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18950 | hp2 | a0001 | c0002 | t0024 | g0076 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0236 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18953 | hp1 | a0001 | c0001 | t0088 | g0144 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18953 | hp2 | a0001 | c0002 | t0010 | g0239 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18954 | hp2 | a0001 | c0001 | t0026 | g0134 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18956 | hp1 | a0001 | c0002 | t0076 | g0074 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18959 | hp2 | a0001 | c0002 | t0068 | g0230 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18960 | hp1 | a0001 | c0002 | t0011 | g0030 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18960 | hp2 | a0001 | c0001 | t0014 | g0199 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18963 | hp1 | a0001 | c0002 | t0010 | g0078 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18967 | hp1 | a0001 | c0001 | t0036 | g0135 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18967 | hp2 | a0001 | c0001 | t0064 | g0273 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18968 | hp1 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18968 | hp2 | a0001 | c0002 | t0024 | g0073 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18974 | hp1 | a0001 | c0002 | t0011 | g0042 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18975 | hp2 | a0001 | c0001 | t0042 | g0106 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18977 | hp1 | a0001 | c0002 | t0067 | g0035 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18979 | hp1 | a0001 | c0002 | t0060 | g0219 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18981 | hp1 | a0001 | c0002 | t0104 | g0048 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18981 | hp2 | a0001 | c0001 | t0075 | g0109 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18983 | hp1 | a0001 | c0002 | t0010 | g0206 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18984 | hp1 | a0001 | c0002 | t0010 | g0205 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18987 | hp1 | a0001 | c0001 | t0019 | g0235 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18990 | hp1 | a0001 | c0002 | t0103 | g0037 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18993 | hp2 | a0001 | c0002 | t0042 | g0217 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19000 | hp1 | a0001 | c0002 | t0028 | g0212 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19000 | hp2 | a0001 | c0001 | t0026 | g0147 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19001 | hp2 | a0001 | c0001 | t0084 | g0090 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19007 | hp1 | a0001 | c0001 | t0025 | g0133 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19010 | hp2 | a0001 | c0001 | t0019 | g0237 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19030 | hp1 | a0001 | c0002 | t0115 | g0018 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19030 | hp2 | a0001 | c0002 | t0121 | g0258 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19043 | hp2 | a0001 | c0002 | t0007 | g0183 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19060 | hp2 | a0001 | c0001 | t0093 | g0234 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19066 | hp1 | a0001 | c0001 | t0107 | g0088 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19067 | hp1 | a0001 | c0001 | t0018 | g0097 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19070 | hp1 | a0001 | c0001 | t0077 | g0122 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19072 | hp1 | a0001 | c0001 | t0025 | g0160 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19072 | hp2 | a0001 | c0002 | t0062 | g0043 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19074 | hp1 | a0001 | c0002 | t0024 | g0077 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19082 | hp1 | a0001 | c0001 | t0087 | g0103 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19088 | hp1 | a0001 | c0001 | t0018 | g0107 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19091 | hp1 | a0001 | c0002 | t0017 | g0222 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19240 | hp1 | a0001 | c0002 | t0032 | g0203 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA19240 | hp2 | a0001 | c0002 | t0045 | g0250 | AFR | YRI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20129 | hp1 | a0001 | c0002 | t0127 | g0308 | AFR | ASW | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20129 | hp2 | a0001 | c0002 | t0128 | g0202 | AFR | ASW | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20752 | hp1 | a0001 | c0002 | t0006 | g0211 | EUR | TSI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20752 | hp2 | a0001 | c0001 | t0033 | g0125 | EUR | TSI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20905 | hp1 | a0001 | c0002 | t0006 | g0187 | SAS | GIH | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01123 | hp1 | a0001 | c0001 | t0100 | g0166 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02109 | hp1 | a0001 | c0002 | t0020 | g0184 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02109 | hp2 | a0001 | c0002 | t0109 | g0179 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02559 | hp1 | a0001 | c0001 | t0053 | g0290 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG02559 | hp2 | a0001 | c0002 | t0048 | g0173 | AFR | ACB | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03471 | hp1 | a0001 | c0002 | t0046 | g0265 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG03471 | hp2 | a0001 | c0002 | t0114 | g0017 | AFR | MSL | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG06807 | hp1 | a0001 | c0002 | t0070 | g0260 | AFR | USA | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
HG06807 | hp2 | a0001 | c0002 | t0117 | g0261 | AFR | USA | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18955 | hp1 | a0001 | c0001 | t0074 | g0143 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | USA | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA20300 | hp2 | a0001 | c0001 | t0038 | g0168 | AFR | USA | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
NA21309 | hp2 | a0001 | c0002 | t0023 | g0253 | AFR | LWK | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0070 | REF | REF | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
homoSapiens | grch38p0 | a0001 | c0001 | t0112 | g0259 | REF | REF | TMEM192_chr4_165065608_165117860 | TMEM192 | chr4 | 165065608 | 165117860 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:165100659 | G | C | 1 | a0001c0002 | 136 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(133): Show |
synonymous_variant | LOW | c.408C>G | p.Leu136Leu | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/6 | 495/9953 | 408/816 | 136/271 | chr4 | 165100659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:165070742 | A | G | 2 | a0001c0001t0064 a0001c0002t0010 |
5 | NA18953.hp2 NA18963.hp1 NA18967.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8916T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8916 | chr4 | 165070742 | ||||||
chr4:165070869 | T | C | 1 | a0001c0001t0085 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8789A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8789 | chr4 | 165070869 | ||||||
chr4:165070877 | A | G | 6 | a0001c0001t0021 a0001c0001t0123 a0001c0002t0024 others(3): Show |
10 | HG01109.hp2 HG02451.hp1 HG02738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8781T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8781 | chr4 | 165070877 | ||||||
chr4:165070991 | A | G | 1 | a0001c0002t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8667T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8667 | chr4 | 165070991 | ||||||
chr4:165071199 | T | C | 1 | a0001c0002t0055 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8459A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8459 | chr4 | 165071199 | ||||||
chr4:165071290 | A | AT | 26 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0020 others(23): Show |
43 | HG00323.hp2 HG01884.hp2 HG01975.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8367dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8367 | chr4 | 165071290 | ||||||
chr4:165071300 | T | G | 2 | a0001c0002t0024 a0001c0002t0131 |
4 | HG02738.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8358A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8358 | chr4 | 165071300 | ||||||
chr4:165071302 | T | G | 1 | a0001c0002t0045 | 2 | HG02922.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8356A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8356 | chr4 | 165071302 | ||||||
chr4:165071302 | T | TG | 9 | a0001c0001t0003 a0001c0001t0028 a0001c0001t0074 others(6): Show |
18 | HG00558.hp2 HG02056.hp1 HG02132.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8355dupC | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8355 | chr4 | 165071302 | ||||||
chr4:165071303 | G | T | 2 | a0001c0002t0024 a0001c0002t0131 |
4 | HG02738.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8355C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8355 | chr4 | 165071303 | ||||||
chr4:165071304 | G | C | 1 | a0001c0001t0035 | 2 | HG02602.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8354C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8354 | chr4 | 165071304 | ||||||
chr4:165071305 | G | C | 2 | a0001c0002t0048 a0001c0002t0126 |
3 | HG01884.hp2 HG02559.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8353C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8353 | chr4 | 165071305 | ||||||
chr4:165071321 | CACTCT | C | 2 | a0001c0002t0048 a0001c0002t0126 |
3 | HG01884.hp2 HG02559.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8332_*8336delAGAG others(1): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8332 | chr4 | 165071321 | ||||||
chr4:165071325 | CT | C | 25 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0020 others(22): Show |
43 | HG00323.hp2 HG01975.hp1 HG02040.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8332delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8332 | chr4 | 165071325 | ||||||
chr4:165071370 | C | T | 10 | a0001c0001t0005 a0001c0001t0094 a0001c0001t0095 others(7): Show |
19 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*8288G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8288 | chr4 | 165071370 | ||||||
chr4:165071420 | T | C | 125 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(122): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*8238A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8238 | chr4 | 165071420 | ||||||
chr4:165071433 | A | G | 2 | a0001c0002t0024 a0001c0002t0131 |
4 | HG02738.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8225T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8225 | chr4 | 165071433 | ||||||
chr4:165071527 | A | G | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(70): Show |
164 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*8131T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8131 | chr4 | 165071527 | ||||||
chr4:165071572 | G | C | 71 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(68): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*8086C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8086 | chr4 | 165071572 | ||||||
chr4:165071643 | T | G | 1 | a0001c0001t0056 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8015A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 8015 | chr4 | 165071643 | ||||||
chr4:165071756 | A | AGGTGG | 3 | a0001c0002t0032 a0001c0002t0097 a0001c0002t0118 |
4 | HG02258.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7897_*7901dupCCAC others(1): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7901 | chr4 | 165071756 | ||||||
chr4:165071756 | A | T | 1 | a0001c0001t0087 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7902T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7902 | chr4 | 165071756 | ||||||
chr4:165071854 | T | G | 9 | a0001c0001t0046 a0001c0001t0105 a0001c0001t0106 others(6): Show |
12 | HG01081.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7804A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7804 | chr4 | 165071854 | ||||||
chr4:165071879 | C | T | 2 | a0001c0002t0024 a0001c0002t0131 |
4 | HG02738.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7779G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7779 | chr4 | 165071879 | ||||||
chr4:165071957 | T | C | 60 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(57): Show |
146 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*7701A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7701 | chr4 | 165071957 | ||||||
chr4:165071993 | A | T | 114 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(111): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*7665T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7665 | chr4 | 165071993 | ||||||
chr4:165072070 | G | A | 10 | a0001c0001t0022 a0001c0001t0105 a0001c0001t0106 others(7): Show |
13 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7588C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7588 | chr4 | 165072070 | ||||||
chr4:165072088 | A | C | 1 | a0001c0001t0087 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7570T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7570 | chr4 | 165072088 | ||||||
chr4:165072154 | C | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
112 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*7504G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7504 | chr4 | 165072154 | ||||||
chr4:165072180 | G | A | 7 | a0001c0001t0039 a0001c0001t0040 a0001c0001t0098 others(4): Show |
7 | HG01123.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7478C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7478 | chr4 | 165072180 | ||||||
chr4:165072214 | A | G | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*7444T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7444 | chr4 | 165072214 | ||||||
chr4:165072229 | AAAAG | A | 2 | a0001c0001t0014 a0001c0002t0014 |
4 | HG00673.hp1 HG00673.hp2 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7425_*7428delCTTT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7425 | chr4 | 165072229 | ||||||
chr4:165072406 | A | G | 112 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(109): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*7252T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7252 | chr4 | 165072406 | ||||||
chr4:165072418 | G | T | 4 | a0001c0001t0008 a0001c0001t0065 a0001c0001t0086 others(1): Show |
8 | HG00323.hp1 HG01074.hp2 HG01192.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7240C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7240 | chr4 | 165072418 | ||||||
chr4:165072488 | C | T | 2 | a0001c0001t0012 a0001c0001t0101 |
5 | HG00735.hp2 HG01358.hp1 HG01993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7170G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7170 | chr4 | 165072488 | ||||||
chr4:165072511 | C | T | 1 | a0001c0002t0079 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7147G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7147 | chr4 | 165072511 | ||||||
chr4:165072553 | TC | T | 100 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(97): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*7104delG | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7104 | chr4 | 165072553 | ||||||
chr4:165072557 | C | A | 10 | a0001c0001t0028 a0001c0001t0036 a0001c0001t0064 others(7): Show |
11 | HG00621.hp2 HG02056.hp1 HG03195.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7101G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7101 | chr4 | 165072557 | ||||||
chr4:165072557 | C | CA | 5 | a0001c0001t0100 a0001c0002t0044 a0001c0002t0051 others(2): Show |
6 | HG01123.hp1 HG02572.hp1 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7100_*7101insT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7100 | chr4 | 165072557 | ||||||
chr4:165072558 | C | A | 139 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(136): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*7100G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7100 | chr4 | 165072558 | ||||||
chr4:165072577 | C | T | 1 | a0001c0001t0125 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7081G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7081 | chr4 | 165072577 | ||||||
chr4:165072603 | G | A | 1 | a0001c0002t0059 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7055C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 7055 | chr4 | 165072603 | ||||||
chr4:165072816 | T | C | 1 | a0001c0002t0115 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6842A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6842 | chr4 | 165072816 | ||||||
chr4:165072838 | G | C | 1 | a0001c0001t0089 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6820C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6820 | chr4 | 165072838 | ||||||
chr4:165072842 | A | C | 1 | a0001c0002t0108 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6816T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6816 | chr4 | 165072842 | ||||||
chr4:165073008 | A | G | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*6650T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6650 | chr4 | 165073008 | ||||||
chr4:165073253 | A | C | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0002t0022 |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6405T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6405 | chr4 | 165073253 | ||||||
chr4:165073389 | C | G | 1 | a0001c0001t0052 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6269G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6269 | chr4 | 165073389 | ||||||
chr4:165073431 | G | A | 1 | a0001c0002t0110 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6227C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6227 | chr4 | 165073431 | ||||||
chr4:165073655 | G | A | 1 | a0001c0001t0075 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6003C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 6003 | chr4 | 165073655 | ||||||
chr4:165073745 | G | T | 1 | a0001c0001t0095 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5913C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5913 | chr4 | 165073745 | ||||||
chr4:165073840 | T | C | 1 | a0001c0002t0116 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5818A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5818 | chr4 | 165073840 | ||||||
chr4:165073954 | A | G | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*5704T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5704 | chr4 | 165073954 | ||||||
chr4:165074083 | C | T | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0002t0022 |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5575G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5575 | chr4 | 165074083 | ||||||
chr4:165074113 | A | AC | 19 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0040 others(16): Show |
22 | HG01123.hp1 HG02258.hp1 HG02723.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5544dupG | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5544 | chr4 | 165074113 | ||||||
chr4:165074113 | A | ACC | 91 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(88): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*5543_*5544dupGG | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5544 | chr4 | 165074113 | ||||||
chr4:165074169 | T | C | 2 | a0001c0001t0040 a0001c0002t0040 |
2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5489A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5489 | chr4 | 165074169 | ||||||
chr4:165074298 | T | C | 2 | a0001c0001t0123 a0001c0002t0124 |
2 | HG01109.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5360A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5360 | chr4 | 165074298 | ||||||
chr4:165074309 | G | A | 125 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(122): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*5349C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5349 | chr4 | 165074309 | ||||||
chr4:165074424 | G | C | 2 | a0001c0002t0032 a0001c0002t0118 |
3 | HG02258.hp1 HG03453.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5234C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5234 | chr4 | 165074424 | ||||||
chr4:165074494 | T | C | 111 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(108): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*5164A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5164 | chr4 | 165074494 | ||||||
chr4:165074501 | C | T | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*5157G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5157 | chr4 | 165074501 | ||||||
chr4:165074553 | TCTC | T | 5 | a0001c0001t0120 a0001c0002t0023 a0001c0002t0045 others(2): Show |
8 | HG01891.hp1 HG02895.hp2 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5102_*5104delGAG | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5102 | chr4 | 165074553 | ||||||
chr4:165074578 | C | G | 2 | a0001c0001t0033 a0001c0001t0078 |
3 | HG00099.hp2 HG03831.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5080G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5080 | chr4 | 165074578 | ||||||
chr4:165074653 | C | T | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*5005G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 5005 | chr4 | 165074653 | ||||||
chr4:165074695 | G | A | 1 | a0001c0002t0061 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4963C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4963 | chr4 | 165074695 | ||||||
chr4:165074698 | C | G | 1 | a0001c0001t0077 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4960G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4960 | chr4 | 165074698 | ||||||
chr4:165074720 | G | A | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*4938C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4938 | chr4 | 165074720 | ||||||
chr4:165074781 | G | A | 1 | a0001c0002t0031 | 2 | HG02622.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4877C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4877 | chr4 | 165074781 | ||||||
chr4:165075005 | G | A | 5 | a0001c0002t0049 a0001c0002t0117 a0001c0002t0121 others(2): Show |
6 | HG03209.hp2 HG03225.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4653C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4653 | chr4 | 165075005 | ||||||
chr4:165075245 | C | CT | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
109 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*4412dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4412 | chr4 | 165075245 | ||||||
chr4:165075245 | CT | C | 9 | a0001c0001t0037 a0001c0002t0037 a0001c0002t0049 others(6): Show |
10 | HG01496.hp1 HG03209.hp2 HG03225.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4412delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4412 | chr4 | 165075245 | ||||||
chr4:165075295 | A | G | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*4363T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4363 | chr4 | 165075295 | ||||||
chr4:165075356 | T | C | 2 | a0001c0001t0065 a0001c0001t0066 |
2 | HG00099.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4302A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4302 | chr4 | 165075356 | ||||||
chr4:165075370 | G | C | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4288C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4288 | chr4 | 165075370 | ||||||
chr4:165075391 | C | T | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*4267G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4267 | chr4 | 165075391 | ||||||
chr4:165075476 | G | A | 1 | a0001c0002t0127 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4182C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4182 | chr4 | 165075476 | ||||||
chr4:165075544 | G | A | 1 | a0001c0001t0092 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4114C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4114 | chr4 | 165075544 | ||||||
chr4:165075573 | A | AT | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
102 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*4084dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4084 | chr4 | 165075573 | ||||||
chr4:165075636 | C | T | 1 | a0001c0001t0094 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4022G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 4022 | chr4 | 165075636 | ||||||
chr4:165075739 | T | C | 2 | a0001c0001t0019 a0001c0001t0093 |
4 | NA18952.hp2 NA18987.hp1 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3919A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3919 | chr4 | 165075739 | ||||||
chr4:165075840 | T | C | 8 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0094 others(5): Show |
15 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3818A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3818 | chr4 | 165075840 | ||||||
chr4:165075864 | G | A | 7 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0094 others(4): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3794C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3794 | chr4 | 165075864 | ||||||
chr4:165075958 | C | A | 2 | a0001c0002t0049 a0001c0002t0129 |
3 | HG03209.hp2 HG03225.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3700G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3700 | chr4 | 165075958 | ||||||
chr4:165075961 | G | T | 1 | a0001c0001t0025 | 2 | NA19007.hp1 NA19072.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3697C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3697 | chr4 | 165075961 | ||||||
chr4:165076026 | T | TA | 4 | a0001c0002t0007 a0001c0002t0114 a0001c0002t0115 others(1): Show |
9 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3631dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3631 | chr4 | 165076026 | ||||||
chr4:165076033 | A | C | 9 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0040 others(6): Show |
10 | HG01123.hp1 HG02723.hp2 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3625T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3625 | chr4 | 165076033 | ||||||
chr4:165076106 | T | C | 2 | a0001c0001t0065 a0001c0001t0066 |
2 | HG00099.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3552A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3552 | chr4 | 165076106 | ||||||
chr4:165076223 | T | G | 52 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(49): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3435A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3435 | chr4 | 165076223 | ||||||
chr4:165076249 | G | A | 21 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0038 others(18): Show |
29 | HG01109.hp2 HG01123.hp1 HG01884.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3409C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3409 | chr4 | 165076249 | ||||||
chr4:165076279 | A | G | 1 | a0001c0001t0072 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3379T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3379 | chr4 | 165076279 | ||||||
chr4:165076486 | G | A | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3172C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3172 | chr4 | 165076486 | ||||||
chr4:165076493 | C | CTATA | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0002t0022 |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3161_*3164dupTATA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 3164 | chr4 | 165076493 | ||||||
chr4:165076694 | A | C | 1 | a0001c0001t0071 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2964 | chr4 | 165076694 | ||||||
chr4:165076706 | G | C | 1 | a0001c0001t0125 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2952C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2952 | chr4 | 165076706 | ||||||
chr4:165076952 | C | G | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2706G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2706 | chr4 | 165076952 | ||||||
chr4:165077223 | C | G | 1 | a0001c0002t0032 | 2 | HG03453.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2435G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2435 | chr4 | 165077223 | ||||||
chr4:165077468 | C | T | 3 | a0001c0001t0130 a0001c0002t0024 a0001c0002t0131 |
5 | HG02738.hp1 HG03688.hp2 NA18950.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2190G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2190 | chr4 | 165077468 | ||||||
chr4:165077515 | G | C | 10 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0039 others(7): Show |
13 | HG01123.hp1 HG02451.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2143C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2143 | chr4 | 165077515 | ||||||
chr4:165077522 | G | A | 1 | a0001c0002t0097 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2136 | chr4 | 165077522 | ||||||
chr4:165077614 | A | G | 1 | a0001c0002t0070 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2044T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 2044 | chr4 | 165077614 | ||||||
chr4:165077689 | G | A | 4 | a0001c0002t0049 a0001c0002t0117 a0001c0002t0128 others(1): Show |
5 | HG03209.hp2 HG03225.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1969 | chr4 | 165077689 | ||||||
chr4:165077823 | C | CA | 6 | a0001c0001t0120 a0001c0002t0023 a0001c0002t0045 others(3): Show |
9 | HG01891.hp1 HG02258.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1834dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1834 | chr4 | 165077823 | ||||||
chr4:165077826 | A | C | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1832T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1832 | chr4 | 165077826 | ||||||
chr4:165077834 | A | C | 132 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(129): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1824T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1824 | chr4 | 165077834 | ||||||
chr4:165077835 | C | A | 1 | a0001c0002t0121 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1823G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1823 | chr4 | 165077835 | ||||||
chr4:165077846 | C | CA | 8 | a0001c0001t0015 a0001c0001t0101 a0001c0001t0102 others(5): Show |
11 | HG01361.hp1 HG01934.hp2 HG01978.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1811dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1811 | chr4 | 165077846 | ||||||
chr4:165077971 | C | T | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1687G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1687 | chr4 | 165077971 | ||||||
chr4:165078033 | A | C | 6 | a0001c0001t0046 a0001c0001t0122 a0001c0001t0123 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1625T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1625 | chr4 | 165078033 | ||||||
chr4:165078150 | T | A | 1 | a0001c0001t0041 | 2 | HG02027.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1508A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1508 | chr4 | 165078150 | ||||||
chr4:165078153 | G | A | 126 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(123): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1505 | chr4 | 165078153 | ||||||
chr4:165078164 | G | A | 1 | a0001c0002t0104 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1494 | chr4 | 165078164 | ||||||
chr4:165078204 | G | A | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1454C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1454 | chr4 | 165078204 | ||||||
chr4:165078399 | C | T | 1 | a0001c0002t0031 | 2 | HG02622.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1259 | chr4 | 165078399 | ||||||
chr4:165078551 | G | C | 1 | a0001c0002t0024 | 3 | NA18950.hp2 NA18968.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1107C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 1107 | chr4 | 165078551 | ||||||
chr4:165078750 | T | C | 3 | a0001c0001t0042 a0001c0001t0107 a0001c0002t0042 |
3 | NA18975.hp2 NA18993.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*908A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 908 | chr4 | 165078750 | ||||||
chr4:165078813 | G | A | 7 | a0001c0002t0047 a0001c0002t0048 a0001c0002t0049 others(4): Show |
10 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*845C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 845 | chr4 | 165078813 | ||||||
chr4:165078875 | C | T | 117 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(114): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*783G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 783 | chr4 | 165078875 | ||||||
chr4:165078890 | C | T | 1 | a0001c0001t0069 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 768 | chr4 | 165078890 | ||||||
chr4:165079043 | A | G | 117 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(114): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 615 | chr4 | 165079043 | ||||||
chr4:165079111 | C | T | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 547 | chr4 | 165079111 | ||||||
chr4:165079129 | C | T | 2 | a0001c0002t0050 a0001c0002t0051 |
2 | HG02683.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*529G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 529 | chr4 | 165079129 | ||||||
chr4:165079165 | C | T | 2 | a0001c0001t0025 a0001c0001t0026 |
4 | NA18954.hp2 NA19000.hp2 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 493 | chr4 | 165079165 | ||||||
chr4:165079270 | T | C | 7 | a0001c0002t0047 a0001c0002t0048 a0001c0002t0049 others(4): Show |
10 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*388A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 388 | chr4 | 165079270 | ||||||
chr4:165079276 | C | A | 3 | a0001c0001t0130 a0001c0002t0024 a0001c0002t0131 |
5 | HG02738.hp1 HG03688.hp2 NA18950.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*382G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 6/6 | 382 | chr4 | 165079276 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:165079934 | T | C | 6 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.678-138A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165079934 | |||||||
chr4:165079998 | A | T | 10 | a0001c0002t0047g0256 a0001c0002t0047g0306 a0001c0002t0048g0173 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.678-202T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165079998 | |||||||
chr4:165080113 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.678-317G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080113 | |||||||
chr4:165080158 | C | T | 1 | a0001c0001t0123g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.678-362G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080158 | |||||||
chr4:165080269 | C | T | 2 | a0001c0002t0031g0201 a0001c0002t0031g0238 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.678-473G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080269 | |||||||
chr4:165080482 | A | C | 10 | a0001c0002t0047g0256 a0001c0002t0047g0306 a0001c0002t0048g0173 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.678-686T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080482 | |||||||
chr4:165080859 | C | T | 1 | a0001c0002t0002g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.678-1063G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080859 | |||||||
chr4:165080914 | C | G | 13 | a0001c0001t0005g0170 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.678-1118G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165080914 | |||||||
chr4:165081006 | C | T | 1 | a0001c0001t0099g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.678-1210G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081006 | |||||||
chr4:165081026 | T | G | 1 | a0001c0002t0007g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.678-1230A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081026 | |||||||
chr4:165081084 | G | A | 92 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.678-1288C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081084 | |||||||
chr4:165081231 | C | T | 2 | a0001c0001t0105g0262 a0001c0001t0106g0263 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.678-1435G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081231 | |||||||
chr4:165081235 | C | CT | 260 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.678-1440dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081235 | |||||||
chr4:165081342 | C | T | 2 | a0001c0001t0004g0006 a0001c0001t0004g0159 |
3 | NA18612.hp1 NA18963.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.678-1546G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081342 | |||||||
chr4:165081355 | T | C | 12 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0047g0256 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.678-1559A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081355 | |||||||
chr4:165081361 | C | T | 2 | a0001c0001t0123g0058 a0001c0002t0124g0024 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.678-1565G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081361 | |||||||
chr4:165081388 | A | T | 2 | a0001c0001t0022g0023 a0001c0002t0097g0249 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.678-1592T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081388 | |||||||
chr4:165081393 | T | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0243 |
2 | HG00609.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.678-1597A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081393 | |||||||
chr4:165081465 | ACTCCGCC others(2431): Show |
A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.677+1683_678-1670d others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081465 | |||||||
chr4:165081682 | T | C | 11 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.678-1886A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165081682 | |||||||
chr4:165082555 | G | A | 11 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.678-2759C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165082555 | |||||||
chr4:165082986 | C | T | 11 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.677+2600G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165082986 | |||||||
chr4:165083047 | C | G | 6 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+2539G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165083047 | |||||||
chr4:165083087 | T | G | 1 | a0001c0002t0117g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677+2499A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165083087 | |||||||
chr4:165083111 | A | G | 6 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+2475T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165083111 | |||||||
chr4:165084347 | C | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.677+1239G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084347 | |||||||
chr4:165084400 | T | A | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1186A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084400 | |||||||
chr4:165084401 | G | C | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1185C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084401 | |||||||
chr4:165084403 | T | A | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1183A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084403 | |||||||
chr4:165084405 | G | A | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1181C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084405 | |||||||
chr4:165084406 | C | T | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1180G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084406 | |||||||
chr4:165084412 | T | G | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1174A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084412 | |||||||
chr4:165084413 | G | T | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1173C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084413 | |||||||
chr4:165084416 | C | T | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1170G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084416 | |||||||
chr4:165084534 | G | A | 5 | a0001c0001t0130g0154 a0001c0002t0024g0073 a0001c0002t0024g0076 others(2): Show |
5 | HG02738.hp1 HG03688.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.677+1052C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084534 | |||||||
chr4:165084536 | C | T | 1 | a0001c0001t0122g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.677+1050G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084536 | |||||||
chr4:165084678 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.677+908C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084678 | |||||||
chr4:165084712 | C | A | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+874G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084712 | |||||||
chr4:165084713 | A | G | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+873T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084713 | |||||||
chr4:165084714 | G | C | 1 | a0001c0001t0036g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+872C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084714 | |||||||
chr4:165084725 | A | G | 13 | a0001c0001t0005g0170 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677+861T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084725 | |||||||
chr4:165084887 | G | A | 3 | a0001c0002t0024g0073 a0001c0002t0024g0076 a0001c0002t0024g0077 |
3 | NA18950.hp2 NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.677+699C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165084887 | |||||||
chr4:165085023 | C | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(11): Show |
17 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.677+563G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085023 | |||||||
chr4:165085049 | C | T | 2 | a0001c0001t0123g0058 a0001c0002t0124g0024 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.677+537G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085049 | |||||||
chr4:165085245 | C | T | 2 | a0001c0001t0123g0058 a0001c0002t0124g0024 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.677+341G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085245 | |||||||
chr4:165085273 | CA | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(230): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.677+312delT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085273 | |||||||
chr4:165085310 | G | C | 1 | a0001c0002t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.677+276C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085310 | |||||||
chr4:165085521 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.677+65T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 5/5 | chr4 | 165085521 | |||||||
chr4:165085846 | C | T | 4 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0125g0079 others(1): Show |
4 | HG01081.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-158G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165085846 | |||||||
chr4:165085847 | A | C | 6 | a0001c0001t0002g0020 a0001c0001t0002g0283 a0001c0001t0002g0286 others(3): Show |
6 | NA18946.hp1 NA18949.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.575-159T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165085847 | |||||||
chr4:165085989 | G | A | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.575-301C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165085989 | |||||||
chr4:165086058 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.575-370C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086058 | |||||||
chr4:165086089 | A | G | 2 | a0001c0002t0031g0201 a0001c0002t0031g0238 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.575-401T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086089 | |||||||
chr4:165086117 | C | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.575-429G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086117 | |||||||
chr4:165086297 | G | C | 2 | a0001c0001t0012g0101 a0001c0001t0101g0099 |
2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.575-609C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086297 | |||||||
chr4:165086418 | C | CT | 35 | a0001c0001t0006g0130 a0001c0001t0006g0145 a0001c0001t0043g0022 others(32): Show |
36 | HG00323.hp2 HG01891.hp1 HG02040.hp1 others(33): Show |
intron_variant | MODIFIER | c.575-731dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086418 | |||||||
chr4:165086418 | CT | C | 94 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(91): Show |
103 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.575-731delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086418 | |||||||
chr4:165086418 | CTT | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(175): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.575-732_575-731del others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086418 | |||||||
chr4:165086567 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.575-879C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086567 | |||||||
chr4:165086592 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.575-904A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086592 | |||||||
chr4:165086613 | C | T | 11 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.575-925G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086613 | |||||||
chr4:165086881 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(11): Show |
17 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.575-1193T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165086881 | |||||||
chr4:165087029 | G | A | 1 | a0001c0001t0020g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.575-1341C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087029 | |||||||
chr4:165087045 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.575-1357G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087045 | |||||||
chr4:165087070 | C | T | 1 | a0001c0002t0007g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.575-1382G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087070 | |||||||
chr4:165087080 | C | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0080g0153 |
3 | HG02015.hp1 HG02132.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.574+1388G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087080 | |||||||
chr4:165087259 | A | T | 1 | a0001c0002t0076g0074 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.574+1209T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087259 | |||||||
chr4:165087326 | T | C | 2 | a0001c0001t0022g0023 a0001c0002t0097g0249 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.574+1142A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087326 | |||||||
chr4:165087417 | A | G | 5 | a0001c0001t0130g0154 a0001c0002t0024g0073 a0001c0002t0024g0076 others(2): Show |
5 | HG02738.hp1 HG03688.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.574+1051T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087417 | |||||||
chr4:165087439 | G | A | 1 | a0001c0002t0128g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.574+1029C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087439 | |||||||
chr4:165087599 | G | A | 5 | a0001c0001t0130g0154 a0001c0002t0024g0073 a0001c0002t0024g0076 others(2): Show |
5 | HG02738.hp1 HG03688.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.574+869C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087599 | |||||||
chr4:165087638 | G | A | 1 | a0001c0001t0125g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.574+830C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087638 | |||||||
chr4:165087650 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.574+818G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087650 | |||||||
chr4:165087667 | C | CGGT | 12 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(9): Show |
12 | HG01123.hp1 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.574+798_574+800dup others(3): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087667 | |||||||
chr4:165087715 | G | A | 1 | a0001c0001t0099g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.574+753C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087715 | |||||||
chr4:165087719 | C | A | 1 | a0001c0001t0095g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.574+749G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087719 | |||||||
chr4:165087727 | G | A | 2 | a0001c0002t0002g0045 a0001c0002t0002g0214 |
2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.574+741C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087727 | |||||||
chr4:165087746 | C | G | 1 | a0001c0001t0038g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.574+722G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087746 | |||||||
chr4:165087801 | T | G | 1 | a0001c0002t0097g0249 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.574+667A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165087801 | |||||||
chr4:165088006 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.574+462G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165088006 | |||||||
chr4:165088148 | T | A | 2 | a0001c0001t0012g0105 a0001c0001t0012g0193 |
2 | HG00735.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.574+320A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165088148 | |||||||
chr4:165088155 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.574+313A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165088155 | |||||||
chr4:165088419 | A | G | 1 | a0001c0002t0047g0306 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.574+49T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 4/5 | chr4 | 165088419 | |||||||
chr4:165088886 | A | T | 12 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0047g0256 others(9): Show |
12 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.440-284T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165088886 | |||||||
chr4:165088932 | C | T | 2 | a0001c0002t0049g0264 a0001c0002t0049g0267 |
2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.440-330G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165088932 | |||||||
chr4:165088968 | G | A | 13 | a0001c0001t0005g0170 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.440-366C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165088968 | |||||||
chr4:165089040 | CA | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(231): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.440-439delT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089040 | |||||||
chr4:165089040 | CAA | C | 14 | a0001c0001t0083g0312 a0001c0001t0123g0058 a0001c0002t0002g0215 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.440-440_440-439del others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089040 | |||||||
chr4:165089040 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0105g0262 a0001c0001t0106g0263 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.440-450_440-439del others(12): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089040 | |||||||
chr4:165089067 | G | T | 2 | a0001c0001t0009g0232 a0001c0001t0092g0102 |
2 | HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.440-465C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089067 | |||||||
chr4:165089081 | A | C | 2 | a0001c0002t0032g0203 a0001c0002t0032g0204 |
2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-479T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089081 | |||||||
chr4:165089345 | G | T | 1 | a0001c0001t0009g0231 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.440-743C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089345 | |||||||
chr4:165089447 | G | A | 115 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(112): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.440-845C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089447 | |||||||
chr4:165089466 | C | T | 2 | a0001c0002t0045g0250 a0001c0002t0045g0255 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.440-864G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089466 | |||||||
chr4:165089524 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.440-922G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089524 | |||||||
chr4:165089525 | G | A | 8 | a0001c0001t0120g0120 a0001c0002t0023g0248 a0001c0002t0023g0252 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-923C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089525 | |||||||
chr4:165089569 | C | T | 12 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(9): Show |
12 | HG01123.hp1 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.440-967G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089569 | |||||||
chr4:165089574 | C | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.440-972G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089574 | |||||||
chr4:165089663 | G | A | 92 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.440-1061C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089663 | |||||||
chr4:165089708 | G | C | 1 | a0001c0001t0008g0155 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.440-1106C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089708 | |||||||
chr4:165089756 | C | T | 1 | a0001c0002t0070g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.440-1154G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089756 | |||||||
chr4:165089764 | A | G | 1 | a0001c0002t0004g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.440-1162T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089764 | |||||||
chr4:165089794 | T | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(11): Show |
17 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.440-1192A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089794 | |||||||
chr4:165089865 | G | A | 1 | a0001c0001t0122g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.440-1263C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089865 | |||||||
chr4:165089947 | C | T | 4 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0125g0079 others(1): Show |
4 | HG01081.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-1345G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165089947 | |||||||
chr4:165090041 | A | G | 1 | a0001c0002t0044g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440-1439T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090041 | |||||||
chr4:165090165 | C | T | 2 | a0001c0001t0034g0108 a0001c0001t0034g0119 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.440-1563G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090165 | |||||||
chr4:165090211 | T | TG | 6 | a0001c0001t0001g0300 a0001c0001t0014g0092 a0001c0001t0042g0106 others(3): Show |
6 | HG03516.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-1610dupC | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090211 | |||||||
chr4:165090213 | G | GA | 87 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
96 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.440-1612dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090213 | G | GAA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(20): Show |
26 | HG00408.hp2 HG00741.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.440-1613_440-1612d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090213 | G | GGA | 116 | a0001c0001t0001g0013 a0001c0001t0001g0066 a0001c0001t0001g0089 others(113): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.440-1612_440-1611i others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090213 | G | GGAA | 25 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0067 others(22): Show |
25 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.440-1612_440-1611i others(5): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090213 | GA | G | 7 | a0001c0001t0130g0154 a0001c0002t0006g0200 a0001c0002t0024g0073 others(4): Show |
7 | HG02280.hp1 HG02738.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-1612delT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090213 | GAAAAAAA others(1): Show |
G | 7 | a0001c0002t0007g0003 a0001c0002t0007g0016 a0001c0002t0007g0171 others(4): Show |
8 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-1619_440-1612d others(10): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090213 | |||||||
chr4:165090215 | A | G | 1 | a0001c0002t0070g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.440-1613T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090215 | |||||||
chr4:165090296 | T | C | 2 | a0001c0001t0028g0158 a0001c0002t0062g0043 |
2 | HG02056.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.440-1694A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090296 | |||||||
chr4:165090549 | A | G | 2 | a0001c0001t0123g0058 a0001c0002t0124g0024 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.440-1947T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090549 | |||||||
chr4:165090654 | C | A | 1 | a0001c0002t0002g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.440-2052G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090654 | |||||||
chr4:165090762 | G | A | 1 | a0001c0001t0106g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.440-2160C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090762 | |||||||
chr4:165090795 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0080g0153 |
3 | HG02015.hp1 HG02132.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.440-2193A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090795 | |||||||
chr4:165090889 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.440-2287G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090889 | |||||||
chr4:165090910 | C | CAAAAAAA | 73 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0020 others(70): Show |
80 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.440-2315_440-2309d others(9): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165090910 | C | CAAAAAAA others(1): Show |
19 | a0001c0001t0002g0002 a0001c0001t0002g0132 a0001c0001t0002g0278 others(16): Show |
21 | HG00621.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.440-2316_440-2309d others(10): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165090910 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0137 others(9): Show |
15 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.440-2317_440-2309d others(11): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165090910 | C | CAAAAAAA others(3): Show |
122 | a0001c0001t0001g0013 a0001c0001t0001g0067 a0001c0001t0001g0089 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.440-2318_440-2309d others(12): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165090910 | C | CAAAAAAA others(4): Show |
40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0066 others(37): Show |
40 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.440-2319_440-2309d others(13): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165090910 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0129g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.440-2321_440-2309d others(15): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165090910 | |||||||
chr4:165091092 | C | T | 3 | a0001c0002t0031g0201 a0001c0002t0031g0238 a0001c0002t0054g0080 |
3 | HG02622.hp2 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.440-2490G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091092 | |||||||
chr4:165091191 | C | T | 4 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0125g0079 others(1): Show |
4 | HG01081.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-2589G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091191 | |||||||
chr4:165091193 | G | A | 11 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0123g0058 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.440-2591C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091193 | |||||||
chr4:165091207 | G | A | 2 | a0001c0002t0006g0180 a0001c0002t0109g0179 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.440-2605C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091207 | |||||||
chr4:165091402 | T | G | 1 | a0001c0002t0097g0249 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.440-2800A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091402 | |||||||
chr4:165091408 | G | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.440-2806C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091408 | |||||||
chr4:165091529 | A | G | 2 | a0001c0002t0032g0203 a0001c0002t0032g0204 |
2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-2927T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091529 | |||||||
chr4:165091534 | C | T | 2 | a0001c0002t0032g0203 a0001c0002t0032g0204 |
2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.440-2932G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091534 | |||||||
chr4:165091762 | A | G | 2 | a0001c0002t0047g0306 a0001c0002t0127g0308 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.440-3160T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091762 | |||||||
chr4:165091764 | G | A | 3 | a0001c0001t0002g0283 a0001c0001t0002g0294 a0001c0001t0064g0273 |
3 | NA18949.hp1 NA18967.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.440-3162C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091764 | |||||||
chr4:165091799 | C | T | 1 | a0001c0001t0008g0309 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.440-3197G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165091799 | |||||||
chr4:165092112 | C | CT | 105 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.440-3511dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | C | CTT | 31 | a0001c0001t0001g0163 a0001c0001t0001g0243 a0001c0001t0001g0274 others(28): Show |
31 | HG00597.hp1 HG00609.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.440-3512_440-3511d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | C | CTTT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0018g0107 others(5): Show |
8 | HG00741.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.440-3513_440-3511d others(5): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | C | CTTTT | 7 | a0001c0001t0105g0262 a0001c0002t0047g0256 a0001c0002t0048g0173 others(4): Show |
7 | HG01884.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-3514_440-3511d others(6): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0031g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.440-3520_440-3511d others(12): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | CT | C | 17 | a0001c0001t0120g0120 a0001c0001t0123g0058 a0001c0001t0125g0079 others(14): Show |
17 | HG01109.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.440-3511delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | CTTTTT | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(9): Show |
15 | HG00408.hp2 HG00735.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.440-3515_440-3511d others(7): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092112 | CTTTTTT | C | 90 | a0001c0001t0001g0148 a0001c0001t0002g0002 a0001c0001t0002g0009 others(87): Show |
99 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.440-3516_440-3511d others(8): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092112 | |||||||
chr4:165092138 | T | TC | 3 | a0001c0001t0074g0143 a0001c0001t0084g0090 a0001c0002t0001g0046 |
3 | HG00621.hp1 NA18955.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.440-3537_440-3536i others(3): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092138 | |||||||
chr4:165092203 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.440-3601G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092203 | |||||||
chr4:165092267 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.440-3665T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092267 | |||||||
chr4:165092382 | A | G | 2 | a0001c0002t0013g0195 a0001c0002t0082g0194 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.440-3780T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092382 | |||||||
chr4:165092401 | C | A | 2 | a0001c0001t0123g0058 a0001c0002t0124g0024 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.440-3799G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092401 | |||||||
chr4:165092484 | T | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.440-3882A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092484 | |||||||
chr4:165092684 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(11): Show |
17 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.440-4082A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092684 | |||||||
chr4:165092787 | A | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(89): Show |
101 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.440-4185T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092787 | |||||||
chr4:165092906 | A | T | 1 | a0001c0001t0018g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.440-4304T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165092906 | |||||||
chr4:165093097 | C | CT | 260 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.440-4496dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093097 | |||||||
chr4:165093100 | T | C | 1 | a0001c0001t0125g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.440-4498A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093100 | |||||||
chr4:165093172 | C | T | 3 | a0001c0001t0042g0106 a0001c0001t0107g0088 a0001c0002t0042g0217 |
3 | NA18975.hp2 NA18993.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.440-4570G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093172 | |||||||
chr4:165093410 | C | T | 2 | a0001c0001t0022g0023 a0001c0002t0097g0249 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.440-4808G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093410 | |||||||
chr4:165093554 | C | G | 2 | a0001c0001t0020g0059 a0001c0001t0020g0060 |
2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.440-4952G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093554 | |||||||
chr4:165093613 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.440-5011A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093613 | |||||||
chr4:165093614 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.440-5012C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093614 | |||||||
chr4:165093647 | A | T | 2 | a0001c0002t0047g0306 a0001c0002t0127g0308 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.440-5045T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093647 | |||||||
chr4:165093716 | T | A | 1 | a0001c0001t0004g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.440-5114A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093716 | |||||||
chr4:165093719 | T | C | 1 | a0001c0001t0072g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.440-5117A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093719 | |||||||
chr4:165093735 | T | C | 1 | a0001c0002t0004g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.440-5133A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165093735 | |||||||
chr4:165094208 | C | T | 1 | a0001c0002t0047g0306 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.440-5606G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094208 | |||||||
chr4:165094237 | A | G | 4 | a0001c0001t0046g0025 a0001c0001t0122g0021 a0001c0001t0125g0079 others(1): Show |
4 | HG01081.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-5635T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094237 | |||||||
chr4:165094372 | G | C | 126 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-5770C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094372 | |||||||
chr4:165094464 | C | T | 2 | a0001c0001t0039g0165 a0001c0001t0100g0166 |
2 | HG01123.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.440-5862G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094464 | |||||||
chr4:165094600 | T | C | 2 | a0001c0002t0031g0201 a0001c0002t0031g0238 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.440-5998A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094600 | |||||||
chr4:165094673 | A | G | 1 | a0001c0001t0087g0103 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.439+5955T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094673 | |||||||
chr4:165094974 | C | CA | 8 | a0001c0001t0002g0272 a0001c0002t0007g0003 a0001c0002t0007g0015 others(5): Show |
9 | HG01934.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+5653dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094974 | |||||||
chr4:165094974 | CA | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.439+5653delT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165094974 | |||||||
chr4:165095417 | C | T | 3 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0128g0202 |
3 | HG03453.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.439+5211G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095417 | |||||||
chr4:165095499 | C | G | 4 | a0001c0001t0022g0023 a0001c0001t0122g0021 a0001c0001t0125g0079 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+5129G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095499 | |||||||
chr4:165095608 | T | C | 4 | a0001c0002t0047g0306 a0001c0002t0048g0173 a0001c0002t0048g0307 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+5020A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095608 | |||||||
chr4:165095625 | C | G | 4 | a0001c0002t0006g0180 a0001c0002t0006g0200 a0001c0002t0044g0181 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+5003G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095625 | |||||||
chr4:165095640 | T | C | 1 | a0001c0002t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.439+4988A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095640 | |||||||
chr4:165095732 | C | T | 1 | a0001c0002t0020g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439+4896G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095732 | |||||||
chr4:165095778 | A | T | 1 | a0001c0002t0002g0075 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.439+4850T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095778 | |||||||
chr4:165095782 | A | T | 2 | a0001c0001t0105g0262 a0001c0001t0106g0263 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.439+4846T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095782 | |||||||
chr4:165095825 | A | T | 42 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(39): Show |
47 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.439+4803T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095825 | |||||||
chr4:165095845 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.439+4783C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095845 | |||||||
chr4:165095949 | A | G | 4 | a0001c0001t0083g0312 a0001c0001t0105g0262 a0001c0001t0106g0263 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+4679T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095949 | |||||||
chr4:165095950 | A | AT | 6 | a0001c0001t0001g0274 a0001c0001t0002g0020 a0001c0002t0006g0200 others(3): Show |
6 | HG00597.hp1 HG02280.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+4677dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095950 | |||||||
chr4:165095950 | AT | A | 6 | a0001c0001t0002g0167 a0001c0001t0002g0295 a0001c0001t0038g0164 others(3): Show |
6 | HG01123.hp1 HG01358.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+4677delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095950 | |||||||
chr4:165095950 | ATT | A | 19 | a0001c0001t0001g0299 a0001c0001t0028g0158 a0001c0001t0090g0063 others(16): Show |
19 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.439+4676_439+4677d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095950 | |||||||
chr4:165095950 | ATTT | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.439+4675_439+4677d others(5): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095950 | |||||||
chr4:165095953 | T | TTTTTTTT others(7051): Show |
1 | a0001c0001t0030g0123 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.439+4674_439+4675i others(7060): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095953 | |||||||
chr4:165095984 | A | T | 66 | a0001c0001t0011g0242 a0001c0001t0011g0268 a0001c0002t0001g0004 others(63): Show |
70 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.439+4644T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165095984 | |||||||
chr4:165096007 | GGCCTGTC others(25): Show |
G | 1 | a0001c0002t0061g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.439+4589_439+4620d others(34): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096007 | |||||||
chr4:165096117 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(8): Show |
14 | HG00408.hp2 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.439+4511T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096117 | |||||||
chr4:165096278 | C | T | 132 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(129): Show |
137 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.439+4350G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096278 | |||||||
chr4:165096313 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.439+4315C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096313 | |||||||
chr4:165096356 | G | A | 1 | a0001c0001t0106g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.439+4272C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096356 | |||||||
chr4:165096411 | T | TTA | 5 | a0001c0001t0022g0023 a0001c0001t0043g0022 a0001c0001t0077g0122 others(2): Show |
5 | HG02257.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+4215_439+4216d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096411 | |||||||
chr4:165096588 | G | A | 1 | a0001c0002t0124g0024 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.439+4040C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096588 | |||||||
chr4:165096629 | C | CT | 130 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
132 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.439+3998dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096629 | |||||||
chr4:165096655 | A | C | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.439+3973T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096655 | |||||||
chr4:165096661 | T | C | 1 | a0001c0002t0127g0308 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.439+3967A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096661 | |||||||
chr4:165096842 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.439+3786T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096842 | |||||||
chr4:165096961 | C | CT | 308 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.439+3666dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096961 | |||||||
chr4:165096978 | G | C | 10 | a0001c0002t0001g0072 a0001c0002t0002g0075 a0001c0002t0024g0073 others(7): Show |
10 | HG00597.hp2 HG01255.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.439+3650C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165096978 | |||||||
chr4:165097027 | T | C | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.439+3601A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097027 | |||||||
chr4:165097051 | A | G | 4 | a0001c0001t0022g0023 a0001c0001t0043g0022 a0001c0001t0122g0021 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+3577T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097051 | |||||||
chr4:165097078 | C | A | 6 | a0001c0001t0001g0136 a0001c0001t0025g0133 a0001c0001t0025g0160 others(3): Show |
6 | NA18954.hp2 NA18967.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+3550G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097078 | |||||||
chr4:165097270 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(61): Show |
68 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.439+3358C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097270 | |||||||
chr4:165097277 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.439+3351T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097277 | |||||||
chr4:165097295 | C | T | 133 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(130): Show |
138 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.439+3333G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097295 | |||||||
chr4:165097367 | G | C | 1 | a0001c0001t0043g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.439+3261C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097367 | |||||||
chr4:165097419 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.439+3209C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097419 | |||||||
chr4:165097437 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0015g0065 a0001c0001t0037g0064 |
3 | HG01192.hp2 HG01496.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.439+3191A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097437 | |||||||
chr4:165097491 | CTCAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0316 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.439+3125_439+3136d others(14): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097491 | |||||||
chr4:165097493 | C | CA | 10 | a0001c0001t0005g0177 a0001c0001t0006g0145 a0001c0001t0036g0135 others(7): Show |
11 | HG02280.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.439+3134dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097493 | |||||||
chr4:165097493 | C | CAA | 120 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(117): Show |
124 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.439+3133_439+3134d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097493 | |||||||
chr4:165097493 | C | CAAA | 6 | a0001c0002t0001g0027 a0001c0002t0001g0072 a0001c0002t0017g0225 others(3): Show |
6 | HG00597.hp2 HG02970.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+3132_439+3134d others(5): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097493 | |||||||
chr4:165097568 | C | A | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.439+3060G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097568 | |||||||
chr4:165097569 | C | CT | 93 | a0001c0001t0002g0270 a0001c0001t0003g0282 a0001c0001t0012g0101 others(90): Show |
95 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.439+3058dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097569 | |||||||
chr4:165097585 | T | TG | 36 | a0001c0002t0002g0007 a0001c0002t0002g0045 a0001c0002t0002g0083 others(33): Show |
39 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.439+3042dupC | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097585 | |||||||
chr4:165097666 | G | A | 3 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0128g0202 |
3 | HG03453.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.439+2962C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097666 | |||||||
chr4:165097667 | T | C | 125 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(122): Show |
130 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.439+2961A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097667 | |||||||
chr4:165097701 | A | T | 1 | a0001c0002t0070g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.439+2927T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097701 | |||||||
chr4:165097785 | ATTTAT | A | 8 | a0001c0002t0022g0062 a0001c0002t0031g0238 a0001c0002t0040g0061 others(5): Show |
8 | HG02622.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.439+2838_439+2842d others(7): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097785 | |||||||
chr4:165097839 | T | G | 1 | a0001c0002t0110g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.439+2789A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097839 | |||||||
chr4:165097930 | C | T | 115 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(112): Show |
120 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.439+2698G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165097930 | |||||||
chr4:165098124 | C | G | 1 | a0001c0002t0042g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.439+2504G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098124 | |||||||
chr4:165098155 | G | T | 1 | a0001c0002t0037g0032 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.439+2473C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098155 | |||||||
chr4:165098345 | G | A | 38 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(35): Show |
43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.439+2283C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098345 | |||||||
chr4:165098372 | G | A | 1 | a0001c0001t0006g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.439+2256C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098372 | |||||||
chr4:165098439 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.439+2189A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098439 | |||||||
chr4:165098440 | T | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.439+2188A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098440 | |||||||
chr4:165098441 | A | T | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.439+2187T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098441 | |||||||
chr4:165098491 | G | A | 3 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0128g0202 |
3 | HG03453.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.439+2137C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098491 | |||||||
chr4:165098616 | T | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0098 others(8): Show |
14 | HG00408.hp2 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.439+2012A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098616 | |||||||
chr4:165098718 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(306): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.439+1910C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098718 | |||||||
chr4:165098728 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(61): Show |
68 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.439+1900C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098728 | |||||||
chr4:165098949 | G | A | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.439+1679C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165098949 | |||||||
chr4:165099102 | C | CT | 18 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(15): Show |
18 | HG01081.hp2 HG02451.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.439+1525dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099102 | |||||||
chr4:165099102 | C | CTT | 60 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(57): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.439+1524_439+1525d others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099102 | |||||||
chr4:165099102 | CT | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0149 a0001c0001t0001g0301 others(5): Show |
8 | HG01070.hp1 HG01167.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+1525delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099102 | |||||||
chr4:165099106 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.439+1522A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099106 | |||||||
chr4:165099107 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0149 |
2 | HG01167.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.439+1521A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099107 | |||||||
chr4:165099365 | C | G | 38 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(35): Show |
43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.439+1263G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099365 | |||||||
chr4:165099713 | C | A | 8 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(5): Show |
8 | HG01081.hp2 HG02451.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+915G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099713 | |||||||
chr4:165099762 | T | C | 133 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(130): Show |
138 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.439+866A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099762 | |||||||
chr4:165099890 | A | G | 1 | a0001c0001t0015g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.439+738T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099890 | |||||||
chr4:165099910 | C | G | 1 | a0001c0002t0002g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.439+718G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099910 | |||||||
chr4:165099968 | T | A | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.439+660A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165099968 | |||||||
chr4:165100162 | C | CT | 181 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(178): Show |
191 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.439+465dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165100162 | |||||||
chr4:165100162 | C | CTT | 8 | a0001c0001t0022g0023 a0001c0001t0105g0262 a0001c0001t0106g0263 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.439+464_439+465dup others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165100162 | |||||||
chr4:165100433 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(306): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.439+195A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165100433 | |||||||
chr4:165100510 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.439+118G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165100510 | |||||||
chr4:165100618 | T | C | 1 | a0001c0002t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.439+10A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 3/5 | chr4 | 165100618 | |||||||
chr4:165100959 | C | T | 3 | a0001c0002t0031g0238 a0001c0002t0117g0261 a0001c0002t0121g0258 |
3 | HG02622.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.175-67G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165100959 | |||||||
chr4:165100971 | C | CT | 69 | a0001c0001t0001g0012 a0001c0001t0001g0094 a0001c0001t0001g0098 others(66): Show |
74 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.175-80dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165100971 | |||||||
chr4:165100971 | C | CTT | 6 | a0001c0001t0001g0274 a0001c0001t0002g0283 a0001c0001t0003g0282 others(3): Show |
6 | HG00597.hp1 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-81_175-80dupAA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165100971 | |||||||
chr4:165100971 | CT | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0241 a0001c0001t0019g0237 others(5): Show |
8 | HG04228.hp1 NA18946.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-80delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165100971 | |||||||
chr4:165101063 | A | G | 1 | a0001c0002t0001g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.175-171T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101063 | |||||||
chr4:165101122 | A | G | 131 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(128): Show |
136 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.175-230T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101122 | |||||||
chr4:165101123 | C | T | 4 | a0001c0002t0046g0265 a0001c0002t0049g0264 a0001c0002t0049g0267 others(1): Show |
4 | HG03209.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-231G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101123 | |||||||
chr4:165101125 | C | A | 1 | a0001c0001t0015g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.175-233G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101125 | |||||||
chr4:165101167 | G | A | 1 | a0001c0001t0102g0310 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175-275C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101167 | |||||||
chr4:165101256 | G | A | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.175-364C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101256 | |||||||
chr4:165101311 | G | A | 131 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(128): Show |
136 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.175-419C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101311 | |||||||
chr4:165101335 | T | A | 2 | a0001c0002t0046g0265 a0001c0002t0129g0266 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-443A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101335 | |||||||
chr4:165101347 | C | T | 38 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(35): Show |
43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.175-455G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101347 | |||||||
chr4:165101540 | G | A | 131 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(128): Show |
136 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.175-648C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101540 | |||||||
chr4:165101793 | G | A | 1 | a0001c0001t0006g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175-901C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101793 | |||||||
chr4:165101855 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.175-963T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101855 | |||||||
chr4:165101974 | A | C | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.174+976T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165101974 | |||||||
chr4:165102105 | C | T | 2 | a0001c0001t0122g0021 a0001c0002t0070g0260 |
2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.174+845G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102105 | |||||||
chr4:165102106 | G | A | 64 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(61): Show |
68 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.174+844C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102106 | |||||||
chr4:165102286 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.174+664C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102286 | |||||||
chr4:165102313 | G | A | 1 | a0001c0002t0014g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.174+637C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102313 | |||||||
chr4:165102328 | T | C | 2 | a0001c0002t0006g0211 a0001c0002t0108g0210 |
2 | HG04228.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.174+622A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102328 | |||||||
chr4:165102366 | C | T | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.174+584G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102366 | |||||||
chr4:165102453 | G | T | 1 | a0001c0002t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.174+497C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102453 | |||||||
chr4:165102458 | C | T | 1 | a0001c0001t0098g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+492G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102458 | |||||||
chr4:165102705 | C | T | 7 | a0001c0002t0023g0252 a0001c0002t0023g0253 a0001c0002t0039g0254 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+245G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102705 | |||||||
chr4:165102781 | G | A | 1 | a0001c0001t0015g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.174+169C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102781 | |||||||
chr4:165102784 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.174+165dupA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102784 | |||||||
chr4:165102784 | CT | C | 56 | a0001c0002t0001g0072 a0001c0002t0002g0075 a0001c0002t0002g0186 others(53): Show |
57 | HG00323.hp2 HG00597.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.174+165delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102784 | |||||||
chr4:165102784 | CTT | C | 63 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(60): Show |
67 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.174+164_174+165del others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102784 | |||||||
chr4:165102817 | A | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.174+133T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102817 | |||||||
chr4:165102853 | A | G | 7 | a0001c0002t0001g0072 a0001c0002t0002g0075 a0001c0002t0024g0073 others(4): Show |
7 | HG00597.hp2 HG01255.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+97T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102853 | |||||||
chr4:165102867 | A | C | 1 | a0001c0001t0020g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.174+83T>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 2/5 | chr4 | 165102867 | |||||||
chr4:165103106 | A | G | 5 | a0001c0002t0006g0180 a0001c0002t0006g0200 a0001c0002t0031g0201 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-10T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103106 | |||||||
chr4:165103511 | A | ATTT | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0316 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-418_28-416dupAA others(1): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103511 | |||||||
chr4:165103511 | A | ATTTT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(160): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.28-419_28-416dupAA others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103511 | |||||||
chr4:165103511 | A | ATTTTT | 15 | a0001c0001t0001g0012 a0001c0001t0001g0066 a0001c0001t0001g0089 others(12): Show |
15 | HG00558.hp1 HG00741.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-420_28-416dupAA others(3): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103511 | |||||||
chr4:165103511 | AT | A | 110 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0001g0004 others(107): Show |
115 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.28-416delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103511 | |||||||
chr4:165103639 | TG | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.28-544delC | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103639 | |||||||
chr4:165103742 | G | A | 1 | a0001c0002t0044g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-646C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165103742 | |||||||
chr4:165104116 | G | A | 2 | a0001c0002t0002g0186 a0001c0002t0002g0189 |
2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.28-1020C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104116 | |||||||
chr4:165104199 | T | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG00408.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.28-1103A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104199 | |||||||
chr4:165104238 | A | T | 12 | a0001c0001t0005g0170 a0001c0001t0005g0174 a0001c0001t0005g0175 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-1142T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104238 | |||||||
chr4:165104570 | G | A | 43 | a0001c0002t0002g0186 a0001c0002t0002g0189 a0001c0002t0004g0188 others(40): Show |
44 | HG00323.hp2 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-1474C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104570 | |||||||
chr4:165104703 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.28-1607C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104703 | |||||||
chr4:165104773 | C | T | 1 | a0001c0001t0015g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.28-1677G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104773 | |||||||
chr4:165104881 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.28-1785G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165104881 | |||||||
chr4:165105061 | T | C | 2 | a0001c0002t0022g0062 a0001c0002t0040g0061 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.28-1965A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105061 | |||||||
chr4:165105134 | T | A | 2 | a0001c0001t0105g0262 a0001c0001t0106g0263 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.28-2038A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105134 | |||||||
chr4:165105205 | C | T | 1 | a0001c0001t0056g0280 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.28-2109G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105205 | |||||||
chr4:165105421 | G | A | 62 | a0001c0002t0001g0004 a0001c0002t0001g0027 a0001c0002t0001g0031 others(59): Show |
66 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.28-2325C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105421 | |||||||
chr4:165105441 | C | T | 7 | a0001c0002t0002g0208 a0001c0002t0002g0209 a0001c0002t0010g0078 others(4): Show |
7 | HG02083.hp1 NA18945.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-2345G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105441 | |||||||
chr4:165105696 | T | A | 1 | a0001c0001t0095g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-2600A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105696 | |||||||
chr4:165105896 | G | T | 7 | a0001c0002t0001g0072 a0001c0002t0002g0075 a0001c0002t0024g0073 others(4): Show |
7 | HG00597.hp2 HG01255.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-2800C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105896 | |||||||
chr4:165105969 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.28-2873C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165105969 | |||||||
chr4:165106332 | G | C | 1 | a0001c0001t0072g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-3236C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165106332 | |||||||
chr4:165106378 | C | T | 38 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(35): Show |
43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.28-3282G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165106378 | |||||||
chr4:165106415 | T | C | 2 | a0001c0001t0105g0262 a0001c0001t0106g0263 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.28-3319A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165106415 | |||||||
chr4:165106572 | G | A | 43 | a0001c0002t0002g0186 a0001c0002t0002g0189 a0001c0002t0004g0188 others(40): Show |
44 | HG00323.hp2 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-3476C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165106572 | |||||||
chr4:165106836 | C | A | 1 | a0001c0001t0080g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.28-3740G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165106836 | |||||||
chr4:165107050 | A | G | 4 | a0001c0002t0046g0265 a0001c0002t0049g0264 a0001c0002t0049g0267 others(1): Show |
4 | HG03209.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-3954T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107050 | |||||||
chr4:165107127 | C | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.28-4031G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107127 | |||||||
chr4:165107347 | C | CA | 87 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.28-4252dupT | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107347 | |||||||
chr4:165107405 | C | T | 1 | a0001c0001t0038g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-4309G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107405 | |||||||
chr4:165107423 | G | A | 13 | a0001c0001t0001g0301 a0001c0001t0004g0159 a0001c0001t0012g0193 others(10): Show |
13 | HG01169.hp2 HG01993.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-4327C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107423 | |||||||
chr4:165107430 | C | G | 2 | a0001c0002t0070g0260 a0001c0002t0121g0258 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.28-4334G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107430 | |||||||
chr4:165107522 | T | C | 1 | a0001c0002t0104g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.28-4426A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107522 | |||||||
chr4:165107531 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(308): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.28-4435C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107531 | |||||||
chr4:165107652 | G | T | 1 | a0001c0001t0089g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28-4556C>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107652 | |||||||
chr4:165107695 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.28-4599A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107695 | |||||||
chr4:165107774 | C | A | 1 | a0001c0001t0025g0160 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.28-4678G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107774 | |||||||
chr4:165107792 | G | A | 51 | a0001c0001t0001g0190 a0001c0001t0005g0170 a0001c0001t0005g0174 others(48): Show |
51 | HG00323.hp2 HG00408.hp1 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.28-4696C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107792 | |||||||
chr4:165107850 | T | C | 1 | a0001c0001t0081g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.28-4754A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165107850 | |||||||
chr4:165108045 | C | T | 30 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(27): Show |
32 | HG00621.hp1 HG00673.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.27+4702G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108045 | |||||||
chr4:165108112 | CT | C | 37 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0005g0177 others(34): Show |
38 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+4634delA | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108112 | |||||||
chr4:165108112 | CTT | C | 11 | a0001c0001t0001g0190 a0001c0001t0012g0193 a0001c0001t0014g0199 others(8): Show |
11 | HG00323.hp2 HG01993.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+4633_27+4634del others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108112 | |||||||
chr4:165108112 | CTTTTTTT | C | 34 | a0001c0001t0001g0284 a0001c0001t0001g0292 a0001c0001t0001g0296 others(31): Show |
39 | HG00140.hp1 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.27+4628_27+4634del others(7): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108112 | |||||||
chr4:165108112 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0020g0059 a0001c0001t0020g0060 a0001c0002t0022g0062 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+4624_27+4634del others(11): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108112 | |||||||
chr4:165108136 | TTTTG | T | 8 | a0001c0002t0002g0007 a0001c0002t0002g0226 a0001c0002t0003g0008 others(5): Show |
9 | HG00558.hp2 HG02922.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+4607_27+4610del others(4): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108136 | |||||||
chr4:165108137 | TTTG | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0118 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.27+4607_27+4609del others(3): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108137 | |||||||
chr4:165108138 | TTG | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
98 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.27+4607_27+4608del others(2): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108138 | |||||||
chr4:165108139 | TG | T | 15 | a0001c0001t0001g0001 a0001c0001t0002g0156 a0001c0001t0008g0121 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+4607delC | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108139 | |||||||
chr4:165108158 | T | C | 6 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0046g0265 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+4589A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108158 | |||||||
chr4:165108161 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.27+4586G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108161 | |||||||
chr4:165108278 | C | T | 45 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0008g0309 others(42): Show |
47 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.27+4469G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108278 | |||||||
chr4:165108284 | G | C | 2 | a0001c0002t0006g0200 a0001c0002t0031g0201 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27+4463C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108284 | |||||||
chr4:165108403 | G | A | 95 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0005g0245 others(92): Show |
99 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.27+4344C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108403 | |||||||
chr4:165108408 | A | G | 14 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0094g0247 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+4339T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108408 | |||||||
chr4:165108411 | G | A | 2 | a0001c0002t0022g0062 a0001c0002t0040g0061 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.27+4336C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108411 | |||||||
chr4:165108416 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0270 a0001c0001t0002g0272 others(2): Show |
6 | HG01346.hp1 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+4331G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108416 | |||||||
chr4:165108559 | G | A | 1 | a0001c0001t0036g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+4188C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108559 | |||||||
chr4:165108598 | C | T | 14 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0094g0247 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+4149G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108598 | |||||||
chr4:165108667 | T | C | 7 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(4): Show |
7 | HG01081.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+4080A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108667 | |||||||
chr4:165108761 | G | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(208): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.27+3986C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108761 | |||||||
chr4:165108827 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.27+3920G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108827 | |||||||
chr4:165108970 | T | A | 3 | a0001c0002t0032g0203 a0001c0002t0032g0204 a0001c0002t0128g0202 |
3 | HG03453.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27+3777A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165108970 | |||||||
chr4:165109019 | A | G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0015g0065 others(3): Show |
6 | HG01192.hp2 HG01261.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+3728T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109019 | |||||||
chr4:165109043 | G | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0011g0242 others(1): Show |
4 | HG00609.hp1 HG02015.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+3704C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109043 | |||||||
chr4:165109162 | C | T | 1 | a0001c0002t0131g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.27+3585G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109162 | |||||||
chr4:165109246 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.27+3501C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109246 | |||||||
chr4:165109392 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.27+3355C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109392 | |||||||
chr4:165109607 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(209): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.27+3140G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109607 | |||||||
chr4:165109657 | A | T | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27+3090T>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109657 | |||||||
chr4:165109706 | C | T | 45 | a0001c0001t0001g0190 a0001c0001t0005g0170 a0001c0001t0005g0174 others(42): Show |
46 | HG00323.hp2 HG01884.hp2 HG01993.hp1 others(43): Show |
intron_variant | MODIFIER | c.27+3041G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109706 | |||||||
chr4:165109816 | T | C | 5 | a0001c0001t0002g0167 a0001c0001t0038g0164 a0001c0001t0038g0168 others(2): Show |
5 | HG01123.hp1 HG01358.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+2931A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165109816 | |||||||
chr4:165110039 | T | C | 1 | a0001c0001t0123g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+2708A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110039 | |||||||
chr4:165110051 | T | G | 6 | a0001c0001t0105g0262 a0001c0001t0106g0263 a0001c0002t0046g0265 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+2696A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110051 | |||||||
chr4:165110355 | C | A | 1 | a0001c0001t0018g0169 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.27+2392G>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110355 | |||||||
chr4:165110438 | G | C | 1 | a0001c0001t0011g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.27+2309C>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110438 | |||||||
chr4:165110535 | G | A | 39 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(36): Show |
44 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.27+2212C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110535 | |||||||
chr4:165110660 | G | A | 1 | a0001c0002t0003g0303 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.27+2087C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110660 | |||||||
chr4:165110717 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(112): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.27+2030T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110717 | |||||||
chr4:165110841 | C | T | 1 | a0001c0002t0001g0027 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.27+1906G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165110841 | |||||||
chr4:165111170 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.27+1577C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111170 | |||||||
chr4:165111192 | C | T | 5 | a0001c0001t0020g0059 a0001c0001t0020g0060 a0001c0001t0083g0312 others(2): Show |
5 | HG02145.hp2 HG02698.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+1555G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111192 | |||||||
chr4:165111326 | T | A | 3 | a0001c0002t0047g0306 a0001c0002t0048g0307 a0001c0002t0127g0308 |
3 | HG01884.hp2 HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.27+1421A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111326 | |||||||
chr4:165111346 | G | A | 2 | a0001c0001t0008g0309 a0001c0001t0102g0310 |
2 | HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.27+1401C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111346 | |||||||
chr4:165111471 | C | G | 1 | a0001c0001t0123g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+1276G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111471 | |||||||
chr4:165111504 | A | ACTGCATG | 33 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0057 others(30): Show |
35 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.27+1236_27+1242dup others(7): Show |
TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111504 | |||||||
chr4:165111672 | T | G | 1 | a0001c0002t0119g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.27+1075A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111672 | |||||||
chr4:165111689 | A | G | 6 | a0001c0001t0022g0023 a0001c0001t0043g0022 a0001c0001t0046g0025 others(3): Show |
6 | HG01081.hp2 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+1058T>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111689 | |||||||
chr4:165111703 | T | A | 1 | a0001c0002t0131g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.27+1044A>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165111703 | |||||||
chr4:165112000 | T | C | 1 | a0001c0001t0083g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27+747A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112000 | |||||||
chr4:165112039 | T | C | 1 | a0001c0001t0005g0313 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.27+708A>G | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112039 | |||||||
chr4:165112227 | G | A | 1 | a0001c0001t0009g0314 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.27+520C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112227 | |||||||
chr4:165112252 | C | G | 1 | a0001c0001t0002g0020 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.27+495G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112252 | |||||||
chr4:165112417 | G | A | 1 | a0001c0002t0073g0315 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.27+330C>T | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112417 | |||||||
chr4:165112437 | C | T | 6 | a0001c0002t0007g0003 a0001c0002t0007g0015 a0001c0002t0007g0016 others(3): Show |
7 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+310G>A | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112437 | |||||||
chr4:165112479 | C | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | NA18975.hp1 NA18977.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+268G>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112479 | |||||||
chr4:165112646 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.27+101A>C | TMEM192 | ENSG00000170088.14 | transcript | ENST00000306480.11 | protein_coding | 1/5 | chr4 | 165112646 |