Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9650 |
| ensemblid | ENSG00000066855.16 |
| hgncid | 29510 |
| symbol | MTFR1 |
| name | mitochondrial fission regulator 1 |
| refseq_nuc | NM_014637.4 |
| refseq_prot | NP_055452.3 |
| ensembl_nuc | ENST00000262146.9 |
| ensembl_prot | ENSP00000262146.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 65644734 |
| end | 65710562 |
| strand | + |
| ver | v1.2 |
| region | chr8:65644734-65710562 |
| region5000 | chr8:65639734-65715562 |
| regionname0 | MTFR1_chr8_65644734_65710562 |
| regionname5000 | MTFR1_chr8_65639734_65715562 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 333 | 347 | 84 | 72 | 139 | 14 | 36 | 113 | MTFR1_chr8_65639734_65715562 | MTFR1 | MLGWI others(328): Show |
chr8 | 65639734 | 65715562 |
| a0002 | 0/0 | 164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | MLGWI others(159): Show |
chr8 | 65639734 | 65715562 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 999 | 347 | 84 | 72 | 139 | 14 | 36 | MTFR1_chr8_65639734_65715562 | MTFR1 | ATGCT others(994): Show |
chr8 | 65639734 | 65715562 | ||
| a0002c0002 | 0/0 | 999 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | ATGCT others(994): Show |
chr8 | 65639734 | 65715562 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2651 | 262 | 70 | 52 | 103 | 7 | 28 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0002 | 0/0 | 2651 | 32 | 3 | 10 | 9 | 6 | 4 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0003 | 0/0 | 2647 | 20 | 1 | 5 | 12 | 1 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2642): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0004 | 0/0 | 2651 | 14 | 0 | 2 | 12 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0005 | 0/0 | 2651 | 6 | 6 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0006 | 0/0 | 2651 | 3 | 0 | 2 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0007 | 0/0 | 2649 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2644): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0008 | 0/0 | 2651 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0009 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0010 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0011 | 0/0 | 2647 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2642): Show |
chr8 | 65639734 | 65715562 |
| a0001c0001t0012 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| a0002c0002t0002 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | AAGCT others(2646): Show |
chr8 | 65639734 | 65715562 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0342 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0341 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0137 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02300 | hp2 | a0001 | c0001 | t0010 | g0124 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0144 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0340 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0113 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | LWK | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ASW | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0211 | REF | REF | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0241 | REF | REF | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65704905 | C | T | 1 | a0002 | 1 | NA19088.hp1 | stop_gained | HIGH | c.493C>T | p.Gln165* | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/8 | 624/2651 | 493/1002 | 165/333 | chr8 | 65704905 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65709045 | T | C | 1 | a0001c0001t0009 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1 | chr8 | 65709045 | ||||||
| chr8:65709176 | G | A | 1 | a0001c0001t0006 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*132G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 132 | chr8 | 65709176 | ||||||
| chr8:65709330 | A | G | 1 | a0001c0001t0005 | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*286A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 286 | chr8 | 65709330 | ||||||
| chr8:65709438 | A | C | 1 | a0001c0001t0012 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 394 | chr8 | 65709438 | ||||||
| chr8:65709479 | CGTTT | C | 2 | a0001c0001t0003 a0001c0001t0011 |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*440_*443delGTTT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 440 | INFO_REALIGN_3_PRIME | chr8 | 65709479 | |||||
| chr8:65709557 | G | C | 1 | a0001c0001t0004 | 14 | HG00438.hp2 HG01099.hp2 HG01934.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 513 | chr8 | 65709557 | ||||||
| chr8:65709786 | T | C | 1 | a0001c0001t0011 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 742 | chr8 | 65709786 | ||||||
| chr8:65710001 | C | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(3): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 957 | chr8 | 65710001 | ||||||
| chr8:65710416 | T | G | 1 | a0001c0001t0010 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1372 | chr8 | 65710416 | ||||||
| chr8:65710439 | C | T | 2 | a0001c0001t0005 a0001c0001t0008 |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1395C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1395 | chr8 | 65710439 | ||||||
| chr8:65710544 | CTG | C | 1 | a0001c0001t0007 | 3 | NA18957.hp1 NA18994.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1502_*1503delGT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1502 | INFO_REALIGN_3_PRIME | chr8 | 65710544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65644824 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(2): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81+40G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65644824 | |||||||
| chr8:65645030 | G | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-81+246G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645030 | |||||||
| chr8:65645044 | G | T | 1 | a0001c0001t0001g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-81+260G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645044 | |||||||
| chr8:65645114 | T | A | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+330T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645114 | |||||||
| chr8:65645297 | C | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+513C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645297 | |||||||
| chr8:65645298 | T | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.-81+514T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645298 | |||||||
| chr8:65645422 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+638A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645422 | |||||||
| chr8:65645587 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+803G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645587 | |||||||
| chr8:65645631 | T | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+847T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645631 | |||||||
| chr8:65645689 | C | CT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
45 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-81+908dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645689 | ||||||
| chr8:65645689 | C | CTT | 13 | a0001c0001t0002g0039 a0001c0001t0002g0044 a0001c0001t0002g0045 others(10): Show |
13 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81+907_-81+908dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645689 | ||||||
| chr8:65645692 | T | TC | 33 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0206 others(30): Show |
34 | HG00738.hp1 HG01074.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-81+922dupC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | ||||||
| chr8:65645692 | T | TCC | 52 | a0001c0001t0001g0003 a0001c0001t0001g0141 a0001c0001t0001g0142 others(49): Show |
53 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81+921_-81+922dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | ||||||
| chr8:65645692 | T | TCCC | 16 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0001g0089 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-81+920_-81+922dup others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | ||||||
| chr8:65645692 | T | TTC | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG01261.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-81+908_-81+909ins others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645692 | |||||||
| chr8:65645692 | T | TTTC | 10 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0024 others(7): Show |
10 | HG00642.hp2 HG01346.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81+908_-81+909ins others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645692 | |||||||
| chr8:65645692 | TC | T | 14 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
14 | HG01255.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81+922delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | ||||||
| chr8:65645693 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
51 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-81+909C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645693 | |||||||
| chr8:65645694 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(24): Show |
28 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-81+910C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645694 | |||||||
| chr8:65645705 | C | CCCCCG | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01081.hp2 HG02080.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | ||||||
| chr8:65645705 | C | CCCCG | 39 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(36): Show |
39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | ||||||
| chr8:65645705 | C | CCCG | 14 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(11): Show |
14 | HG02735.hp1 HG03239.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | ||||||
| chr8:65645745 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-81+961C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645745 | |||||||
| chr8:65645917 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-81+1133T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645917 | |||||||
| chr8:65645965 | T | C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+1181T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645965 | |||||||
| chr8:65646025 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-81+1241G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646025 | |||||||
| chr8:65646035 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+1251A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646035 | |||||||
| chr8:65646138 | C | T | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+1354C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646138 | |||||||
| chr8:65646180 | C | T | 8 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81+1396C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646180 | |||||||
| chr8:65646293 | A | G | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG02015.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81+1509A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646293 | |||||||
| chr8:65646596 | G | C | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+1812G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646596 | |||||||
| chr8:65646774 | C | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+1990C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646774 | |||||||
| chr8:65646792 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-81+2008A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646792 | |||||||
| chr8:65646994 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+2210G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646994 | |||||||
| chr8:65647070 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-81+2286A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647070 | |||||||
| chr8:65647173 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-81+2389A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647173 | |||||||
| chr8:65647299 | G | C | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+2515G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647299 | |||||||
| chr8:65647301 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81+2517T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647301 | |||||||
| chr8:65647584 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81+2800A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647584 | |||||||
| chr8:65647806 | CA | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+3033delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647806 | ||||||
| chr8:65647809 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-81+3025A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647809 | |||||||
| chr8:65647823 | C | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+3039C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647823 | |||||||
| chr8:65647997 | A | ATTTG | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+3241_-81+3244d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647997 | ||||||
| chr8:65647997 | ATTTG | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+3241_-81+3244d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647997 | ||||||
| chr8:65648152 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-81+3368G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648152 | |||||||
| chr8:65648167 | C | G | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+3383C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648167 | |||||||
| chr8:65648241 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-81+3457T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648241 | |||||||
| chr8:65648253 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01516.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-81+3469G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648253 | |||||||
| chr8:65648310 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-81+3526C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648310 | |||||||
| chr8:65648547 | A | G | 78 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(75): Show |
78 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-81+3763A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648547 | |||||||
| chr8:65648559 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | NA18947.hp1 NA18955.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-81+3775G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648559 | |||||||
| chr8:65648608 | T | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3824T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648608 | |||||||
| chr8:65648626 | G | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3842G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648626 | |||||||
| chr8:65648639 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3855C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648639 | |||||||
| chr8:65648640 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-81+3856G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648640 | |||||||
| chr8:65648662 | A | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+3878A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648662 | |||||||
| chr8:65648666 | G | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3882G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648666 | |||||||
| chr8:65648699 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3915T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648699 | |||||||
| chr8:65648867 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-81+4083G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648867 | |||||||
| chr8:65649040 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-81+4256T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649040 | |||||||
| chr8:65649064 | TAAAAC | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4283_-81+4287d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65649064 | ||||||
| chr8:65649115 | T | C | 1 | a0001c0001t0012g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-81+4331T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649115 | |||||||
| chr8:65649253 | C | A | 61 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(58): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-81+4469C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649253 | |||||||
| chr8:65649273 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4489C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649273 | |||||||
| chr8:65649309 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81+4525C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649309 | |||||||
| chr8:65649317 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4533T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649317 | |||||||
| chr8:65649341 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81+4557C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649341 | |||||||
| chr8:65649463 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4679T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649463 | |||||||
| chr8:65649524 | T | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(23): Show |
27 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-81+4740T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649524 | |||||||
| chr8:65649875 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+5091G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649875 | |||||||
| chr8:65649899 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(16): Show |
20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81+5115C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649899 | |||||||
| chr8:65649900 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+5116G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649900 | |||||||
| chr8:65650066 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0292 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-81+5282C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650066 | |||||||
| chr8:65650135 | A | C | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02155.hp2 NA18954.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81+5351A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650135 | |||||||
| chr8:65650210 | C | CT | 8 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG02451.hp1 HG04184.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81+5447dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | ||||||
| chr8:65650210 | CT | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
93 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.-81+5447delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | ||||||
| chr8:65650210 | CTT | C | 39 | a0001c0001t0001g0229 a0001c0001t0001g0249 a0001c0001t0001g0250 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.-81+5446_-81+5447d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | ||||||
| chr8:65650258 | C | T | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81+5474C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650258 | |||||||
| chr8:65650280 | C | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+5496C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650280 | |||||||
| chr8:65650317 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-81+5533G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650317 | |||||||
| chr8:65650435 | G | C | 1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-81+5651G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650435 | |||||||
| chr8:65650462 | G | A | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+5678G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650462 | |||||||
| chr8:65650467 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+5683T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650467 | |||||||
| chr8:65650479 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-81+5695C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650479 | |||||||
| chr8:65650833 | C | T | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+6049C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650833 | |||||||
| chr8:65651000 | T | TG | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+6219dupG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651000 | ||||||
| chr8:65651115 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-81+6331A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651115 | |||||||
| chr8:65651302 | TGA | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+6519_-81+6520d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651302 | |||||||
| chr8:65651348 | T | G | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+6564T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651348 | |||||||
| chr8:65651403 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-81+6619A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651403 | |||||||
| chr8:65651657 | A | T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+6873A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651657 | |||||||
| chr8:65651702 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+6918G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651702 | |||||||
| chr8:65651963 | A | AT | 44 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-81+7192dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651963 | ||||||
| chr8:65651963 | A | ATT | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+7191_-81+7192d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651963 | ||||||
| chr8:65652006 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(16): Show |
20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81+7222C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652006 | |||||||
| chr8:65652158 | G | C | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+7374G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652158 | |||||||
| chr8:65652362 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+7578G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652362 | |||||||
| chr8:65652532 | C | A | 1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81+7748C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652532 | |||||||
| chr8:65652564 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-81+7780A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652564 | |||||||
| chr8:65652660 | G | T | 1 | a0001c0001t0001g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-81+7876G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652660 | |||||||
| chr8:65652891 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-81+8107A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652891 | |||||||
| chr8:65652937 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8153C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652937 | |||||||
| chr8:65653123 | T | C | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+8339T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653123 | |||||||
| chr8:65653168 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-81+8384G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653168 | |||||||
| chr8:65653229 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8445T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653229 | |||||||
| chr8:65653230 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8446C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653230 | |||||||
| chr8:65653233 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8449G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653233 | |||||||
| chr8:65653234 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-81+8450C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653234 | |||||||
| chr8:65653266 | T | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+8482T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653266 | |||||||
| chr8:65653327 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-81+8543T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653327 | |||||||
| chr8:65653404 | C | T | 2 | a0001c0001t0004g0081 a0001c0001t0004g0082 |
2 | NA18939.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-81+8620C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653404 | |||||||
| chr8:65653957 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+9173G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653957 | |||||||
| chr8:65653988 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+9204G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653988 | |||||||
| chr8:65654064 | C | CA | 44 | a0001c0001t0001g0094 a0001c0001t0001g0100 a0001c0001t0001g0239 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-81+9298dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654064 | ||||||
| chr8:65654064 | CA | C | 73 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(70): Show |
73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-81+9298delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654064 | ||||||
| chr8:65654153 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-81+9369T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654153 | |||||||
| chr8:65654186 | C | T | 71 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-81+9402C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654186 | |||||||
| chr8:65654255 | T | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9471T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654255 | |||||||
| chr8:65654303 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9519A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654303 | |||||||
| chr8:65654397 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(9): Show |
13 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81+9613C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654397 | |||||||
| chr8:65654478 | T | C | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+9694T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654478 | |||||||
| chr8:65654580 | G | GTGTGT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9808_-81+9812d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654580 | ||||||
| chr8:65654581 | T | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(9): Show |
13 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81+9797T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654581 | |||||||
| chr8:65655027 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0261 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-81+10243C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655027 | |||||||
| chr8:65655148 | C | G | 14 | a0001c0001t0001g0142 a0001c0001t0001g0207 a0001c0001t0001g0216 others(11): Show |
14 | HG02080.hp1 NA18955.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81+10364C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655148 | |||||||
| chr8:65655341 | A | G | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+10557A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655341 | |||||||
| chr8:65655413 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-81+10629T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655413 | |||||||
| chr8:65655418 | G | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02145.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-81+10634G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655418 | |||||||
| chr8:65655581 | A | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-81+10797A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655581 | |||||||
| chr8:65655596 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+10812G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655596 | |||||||
| chr8:65655598 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-81+10814A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655598 | |||||||
| chr8:65655820 | G | A | 1 | a0001c0001t0007g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-81+11036G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655820 | |||||||
| chr8:65655949 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0203 a0001c0001t0004g0202 |
3 | HG02735.hp1 NA18950.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-81+11165_-81+1116 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655949 | |||||||
| chr8:65655951 | A | ATATATAT others(6): Show |
48 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(45): Show |
48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | ATATATAT others(10): Show |
11 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0131 others(8): Show |
11 | HG00621.hp1 HG00621.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(21): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(25): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | ATATATAT others(42): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0285 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(51): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | ATATATAT others(30): Show |
1 | a0001c0001t0004g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(41): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | A | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0183 others(55): Show |
59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-81+11167A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | |||||||
| chr8:65655951 | AATATATA others(14): Show |
A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0048 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81+11180_-81+1120 others(25): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655951 | ||||||
| chr8:65655952 | A | AATATATA others(8): Show |
2 | a0001c0001t0001g0107 a0001c0001t0004g0139 |
2 | HG01106.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-81+11168_-81+1116 others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655952 | |||||||
| chr8:65655952 | ATATATAT others(2): Show |
A | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11169_-81+1117 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655952 | |||||||
| chr8:65655953 | T | A | 45 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(42): Show |
45 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-81+11169T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655953 | |||||||
| chr8:65655954 | A | G | 51 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(48): Show |
51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-81+11170A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655954 | |||||||
| chr8:65655955 | T | A | 12 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(9): Show |
12 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81+11171T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655955 | |||||||
| chr8:65655959 | TATATATA others(4): Show |
T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1119 others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655959 | ||||||
| chr8:65655961 | TATATATA others(2): Show |
T | 4 | a0001c0001t0005g0015 a0001c0001t0006g0340 a0001c0001t0006g0341 others(1): Show |
4 | HG00733.hp1 HG01074.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1119 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655961 | ||||||
| chr8:65655963 | T | A | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11179T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655963 | |||||||
| chr8:65655965 | T | A | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11181T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655965 | |||||||
| chr8:65655966 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0277 |
2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-81+11182A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655966 | |||||||
| chr8:65655967 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-81+11183T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655967 | |||||||
| chr8:65655967 | TACC | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0285 others(5): Show |
8 | HG01934.hp1 HG02486.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655967 | ||||||
| chr8:65655968 | A | AT | 53 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(48): Show |
1 | a0001c0001t0001g0322 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(6): Show |
1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(58): Show |
2 | a0001c0001t0001g0295 a0001c0001t0001g0302 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(69): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(56): Show |
4 | a0001c0001t0001g0293 a0001c0001t0001g0297 a0001c0001t0001g0299 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(67): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(56): Show |
1 | a0001c0001t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(67): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(54): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0296 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATACATAT others(54): Show |
1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0277 |
2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATATATAT others(42): Show |
1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0272 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | A | ATGTATAT others(26): Show |
1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | |||||||
| chr8:65655968 | AC | A | 12 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0131 others(9): Show |
12 | HG00621.hp2 HG01106.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81+11186delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655968 | ||||||
| chr8:65655969 | C | A | 70 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+11185C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CACATATA others(48): Show |
1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(26): Show |
1 | a0001c0001t0001g0337 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(28): Show |
1 | a0001c0001t0001g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(39): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(46): Show |
33 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0235 others(30): Show |
34 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(48): Show |
2 | a0001c0001t0001g0332 a0001c0001t0001g0343 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(44): Show |
5 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0289 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(2): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(4): Show |
5 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0262 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(8): Show |
2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(10): Show |
1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(21): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(20): Show |
1 | a0001c0001t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(31): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(22): Show |
1 | a0001c0001t0001g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(33): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(32): Show |
1 | a0001c0001t0001g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(43): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(34): Show |
2 | a0001c0001t0001g0238 a0001c0001t0001g0257 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(48): Show |
1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(44): Show |
1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(44): Show |
1 | a0001c0001t0001g0306 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(46): Show |
3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 |
3 | HG01891.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(66): Show |
1 | a0001c0001t0001g0264 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(77): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(68): Show |
1 | a0001c0001t0001g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(79): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(48): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0183 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(50): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0226 |
3 | HG02055.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(61): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(52): Show |
1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(63): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(58): Show |
1 | a0001c0001t0001g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(69): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(60): Show |
1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(71): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(62): Show |
1 | a0001c0001t0001g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(73): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(66): Show |
1 | a0001c0001t0001g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(77): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(76): Show |
1 | a0001c0001t0001g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(87): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(54): Show |
1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(28): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(39): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(30): Show |
1 | a0001c0001t0001g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(41): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(34): Show |
1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(46): Show |
1 | a0001c0001t0001g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(48): Show |
1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(62): Show |
1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(73): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(42): Show |
1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(50): Show |
1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(61): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(54): Show |
1 | a0001c0001t0001g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(44): Show |
1 | a0001c0001t0001g0097 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(46): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | NA18944.hp2 NA18957.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(46): Show |
1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(36): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(47): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655969 | C | CATATATA others(54): Show |
1 | a0001c0001t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | |||||||
| chr8:65655970 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
189 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-81+11186C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655970 | |||||||
| chr8:65655986 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11202G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655986 | |||||||
| chr8:65656095 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11311C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656095 | |||||||
| chr8:65656151 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-81+11367A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656151 | |||||||
| chr8:65656187 | ACT | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-81+11406_-81+1140 others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656187 | ||||||
| chr8:65656199 | A | AAAAAC | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
11 | HG01255.hp2 HG01433.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81+11430_-81+1143 others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656199 | ||||||
| chr8:65656266 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11482G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656266 | |||||||
| chr8:65656382 | T | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+11598T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656382 | |||||||
| chr8:65656469 | G | T | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+11685G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656469 | |||||||
| chr8:65656500 | A | AT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0138 others(10): Show |
13 | HG01169.hp2 HG01934.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81+11735dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656500 | ||||||
| chr8:65656540 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11756T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656540 | |||||||
| chr8:65657017 | A | AT | 8 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81+12246dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657017 | ||||||
| chr8:65657020 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-81+12236T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657020 | |||||||
| chr8:65657035 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-81+12251C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657035 | |||||||
| chr8:65657122 | T | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+12338T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657122 | |||||||
| chr8:65657155 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-81+12371A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657155 | |||||||
| chr8:65657249 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+12465G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657249 | |||||||
| chr8:65657331 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-12542A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657331 | |||||||
| chr8:65657357 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12516G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657357 | |||||||
| chr8:65657358 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12515T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657358 | |||||||
| chr8:65657359 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12514T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657359 | |||||||
| chr8:65657360 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12513T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657360 | |||||||
| chr8:65657361 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12512T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657361 | |||||||
| chr8:65657362 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12511T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657362 | |||||||
| chr8:65657363 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12510G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657363 | |||||||
| chr8:65657364 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12509T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657364 | |||||||
| chr8:65657365 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12508T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657365 | |||||||
| chr8:65657366 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12507G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657366 | |||||||
| chr8:65657367 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12506T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657367 | |||||||
| chr8:65657370 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12503T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657370 | |||||||
| chr8:65657371 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12502T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657371 | |||||||
| chr8:65657375 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12498G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657375 | |||||||
| chr8:65657386 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12487C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657386 | |||||||
| chr8:65657389 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12484T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657389 | |||||||
| chr8:65657404 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12469A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657404 | |||||||
| chr8:65657405 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12468G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657405 | |||||||
| chr8:65657407 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12466G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657407 | |||||||
| chr8:65657462 | G | A | 1 | a0001c0001t0007g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-80-12411G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657462 | |||||||
| chr8:65657496 | A | C | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-80-12377A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657496 | |||||||
| chr8:65657515 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0046 |
3 | HG01109.hp2 HG02280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-80-12358C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657515 | |||||||
| chr8:65657606 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-80-12267A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657606 | |||||||
| chr8:65657609 | C | T | 5 | a0001c0001t0001g0260 a0001c0001t0001g0322 a0001c0001t0001g0329 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-12264C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657609 | |||||||
| chr8:65657706 | T | TA | 8 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0184 others(5): Show |
8 | HG02602.hp2 HG02622.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.-80-12152dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657706 | ||||||
| chr8:65657706 | TA | T | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG00733.hp1 HG01074.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-80-12152delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657706 | ||||||
| chr8:65658095 | ATCT | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-11773_-80-1177 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65658095 | ||||||
| chr8:65658132 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11741C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658132 | |||||||
| chr8:65658153 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-11720T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658153 | |||||||
| chr8:65658473 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11400G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658473 | |||||||
| chr8:65658482 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-80-11391T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658482 | |||||||
| chr8:65658690 | A | T | 1 | a0001c0001t0001g0282 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-80-11183A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658690 | |||||||
| chr8:65658695 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11178T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658695 | |||||||
| chr8:65658735 | A | G | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-80-11138A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658735 | |||||||
| chr8:65658800 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-11073G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658800 | |||||||
| chr8:65658912 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-80-10961A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658912 | |||||||
| chr8:65659022 | A | G | 2 | a0001c0001t0008g0011 a0001c0001t0008g0012 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-80-10851A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659022 | |||||||
| chr8:65659041 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-80-10832G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659041 | |||||||
| chr8:65659045 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-80-10828A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659045 | |||||||
| chr8:65659083 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-10790G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659083 | |||||||
| chr8:65659426 | G | GT | 7 | a0001c0001t0001g0093 a0001c0001t0001g0172 a0001c0001t0001g0182 others(4): Show |
7 | HG01928.hp2 HG02622.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-10430dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | ||||||
| chr8:65659426 | G | GTT | 41 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.-80-10431_-80-1043 others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | ||||||
| chr8:65659426 | G | GTTT | 14 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0024 others(11): Show |
14 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-80-10432_-80-1043 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | ||||||
| chr8:65659426 | G | GTTTT | 7 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0031 others(4): Show |
7 | NA18939.hp1 NA18946.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-10433_-80-1043 others(8): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | ||||||
| chr8:65659426 | GT | G | 69 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-80-10430delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | ||||||
| chr8:65659438 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-80-10435T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659438 | |||||||
| chr8:65659456 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-10417C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659456 | |||||||
| chr8:65659498 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-10375G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659498 | |||||||
| chr8:65659599 | C | CG | 4 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0275 others(1): Show |
4 | HG00544.hp1 NA19067.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-10270dupG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659599 | ||||||
| chr8:65659680 | C | T | 77 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-10193C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659680 | |||||||
| chr8:65659957 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
11 | HG01255.hp2 HG01433.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-80-9916C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659957 | |||||||
| chr8:65660215 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-9658T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660215 | |||||||
| chr8:65660291 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 others(27): Show |
31 | HG00408.hp2 HG01168.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-80-9564dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | ||||||
| chr8:65660291 | C | CAAA | 59 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(56): Show |
60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-80-9566_-80-9564d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | ||||||
| chr8:65660291 | CA | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0220 a0001c0001t0001g0283 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-80-9564delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | ||||||
| chr8:65660310 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-80-9563G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660310 | |||||||
| chr8:65660312 | C | CA | 16 | a0001c0001t0001g0199 a0001c0001t0001g0238 a0001c0001t0001g0247 others(13): Show |
16 | HG01081.hp1 HG02148.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-80-9551dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660312 | ||||||
| chr8:65660312 | C | CAA | 31 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.-80-9552_-80-9551d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660312 | ||||||
| chr8:65660312 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-80-9561C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660312 | |||||||
| chr8:65660338 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-80-9535T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660338 | |||||||
| chr8:65660375 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-9498T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660375 | |||||||
| chr8:65660690 | A | G | 2 | a0001c0001t0008g0011 a0001c0001t0008g0012 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-80-9183A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660690 | |||||||
| chr8:65660705 | G | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-9168G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660705 | |||||||
| chr8:65661050 | T | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8823T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661050 | |||||||
| chr8:65661103 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8770A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661103 | |||||||
| chr8:65661212 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0261 a0001c0001t0001g0315 |
3 | HG01168.hp1 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-80-8661G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661212 | |||||||
| chr8:65661326 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-80-8547C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661326 | |||||||
| chr8:65661349 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8524C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661349 | |||||||
| chr8:65661378 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8495C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661378 | |||||||
| chr8:65661380 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0285 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-80-8493G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661380 | |||||||
| chr8:65661512 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-8361C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661512 | |||||||
| chr8:65661546 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-80-8327G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661546 | |||||||
| chr8:65661600 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-80-8273G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661600 | |||||||
| chr8:65661807 | T | C | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-8066T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661807 | |||||||
| chr8:65661964 | AAAAC | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0152 a0001c0001t0001g0269 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-80-7893_-80-7890d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65661964 | ||||||
| chr8:65661980 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7893C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661980 | |||||||
| chr8:65662002 | C | CCTCTCCC others(5): Show |
1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-80-7843_-80-7832d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662002 | ||||||
| chr8:65662022 | T | TCTCTCTC others(3): Show |
4 | a0001c0001t0001g0216 a0001c0001t0001g0243 a0001c0001t0001g0247 others(1): Show |
4 | HG03704.hp1 NA18959.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7822d others(12): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662022 | ||||||
| chr8:65662022 | TCTCTCTC others(3): Show |
T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7822d others(12): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662022 | ||||||
| chr8:65662026 | TCTCTCCC others(77): Show |
T | 33 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(30): Show |
33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-80-7834_-80-7751d others(86): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662026 | ||||||
| chr8:65662032 | C | CCT | 4 | a0001c0001t0001g0107 a0001c0001t0001g0118 a0001c0001t0001g0203 others(1): Show |
4 | HG01106.hp2 HG02735.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-7833_-80-7832d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | ||||||
| chr8:65662032 | C | CCTCTCTC others(7): Show |
52 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0083 others(49): Show |
52 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-80-7832_-80-7831i others(16): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | ||||||
| chr8:65662032 | C | CCTCTCTC others(19): Show |
16 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0112 others(13): Show |
16 | HG00642.hp1 HG01952.hp1 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.-80-7832_-80-7831i others(28): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | ||||||
| chr8:65662032 | C | CCTCTCTC others(31): Show |
1 | a0001c0001t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-80-7832_-80-7831i others(40): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | ||||||
| chr8:65662032 | CCTCTCTC others(5): Show |
C | 7 | a0001c0001t0001g0242 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG01099.hp1 HG01261.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-7812_-80-7801d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | ||||||
| chr8:65662038 | TCTCCCTC others(65): Show |
T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7760d others(74): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662038 | ||||||
| chr8:65662042 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7831C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662042 | |||||||
| chr8:65662044 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7829T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662044 | |||||||
| chr8:65662050 | TCTCCCTC others(28): Show |
T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7819_-80-7785d others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662050 | ||||||
| chr8:65662060 | TCTCTCCC others(18): Show |
T | 1 | a0001c0001t0001g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-80-7769_-80-7745d others(27): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662060 | ||||||
| chr8:65662072 | TTTCCACA others(6): Show |
T | 1 | a0001c0001t0001g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-80-7800_-80-7788d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662072 | |||||||
| chr8:65662150 | G | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-80-7723G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662150 | |||||||
| chr8:65662249 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-80-7624C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662249 | |||||||
| chr8:65662346 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-80-7527A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662346 | |||||||
| chr8:65662360 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-80-7513G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662360 | |||||||
| chr8:65662400 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-80-7473C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662400 | |||||||
| chr8:65662431 | G | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-7442G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662431 | |||||||
| chr8:65662438 | G | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7435G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662438 | |||||||
| chr8:65662491 | G | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7382G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662491 | |||||||
| chr8:65662518 | A | AC | 38 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0105 others(35): Show |
38 | HG00741.hp2 HG01071.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.-80-7351dupC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662518 | ||||||
| chr8:65662534 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7339G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662534 | |||||||
| chr8:65662555 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-7318G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662555 | |||||||
| chr8:65662581 | T | C | 3 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 |
3 | HG03540.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-80-7292T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662581 | |||||||
| chr8:65662605 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7268G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662605 | |||||||
| chr8:65662607 | T | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7266T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662607 | |||||||
| chr8:65662632 | C | CCAT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7240_-80-7239i others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662632 | ||||||
| chr8:65662640 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7233G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662640 | |||||||
| chr8:65662641 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7232A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662641 | |||||||
| chr8:65662653 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7220A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662653 | |||||||
| chr8:65662654 | C | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7219C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662654 | |||||||
| chr8:65662655 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7218C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662655 | |||||||
| chr8:65662663 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7210T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662663 | |||||||
| chr8:65662665 | G | GCCGCCCA others(66): Show |
65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7207_-80-7206i others(75): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662665 | ||||||
| chr8:65662667 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7206A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662667 | |||||||
| chr8:65662668 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7205A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662668 | |||||||
| chr8:65662682 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-80-7191G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662682 | |||||||
| chr8:65662693 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7180C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662693 | |||||||
| chr8:65662699 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7174C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662699 | |||||||
| chr8:65662703 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7170C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662703 | |||||||
| chr8:65662708 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7165G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662708 | |||||||
| chr8:65662711 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7162A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662711 | |||||||
| chr8:65662713 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7160A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662713 | |||||||
| chr8:65662716 | G | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7157G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662716 | |||||||
| chr8:65662753 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7120C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662753 | |||||||
| chr8:65662793 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-80-7080C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662793 | |||||||
| chr8:65662838 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7035A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662838 | |||||||
| chr8:65662843 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7030G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662843 | |||||||
| chr8:65662874 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6999A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662874 | |||||||
| chr8:65662924 | G | A | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-80-6949G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662924 | |||||||
| chr8:65662943 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-6930C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662943 | |||||||
| chr8:65662945 | G | C | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02155.hp2 NA18954.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-80-6928G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662945 | |||||||
| chr8:65662963 | C | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-80-6910C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662963 | |||||||
| chr8:65662988 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6885G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662988 | |||||||
| chr8:65663051 | C | T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-6822C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663051 | |||||||
| chr8:65663063 | A | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-6810A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663063 | |||||||
| chr8:65663180 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-80-6693A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663180 | |||||||
| chr8:65663242 | T | C | 8 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-80-6631T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663242 | |||||||
| chr8:65663246 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6627C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663246 | |||||||
| chr8:65663258 | T | C | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-6615T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663258 | |||||||
| chr8:65663356 | A | G | 3 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0027 |
3 | HG00140.hp1 HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-80-6517A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663356 | |||||||
| chr8:65663393 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6480T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663393 | |||||||
| chr8:65663394 | G | C | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-6479G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663394 | |||||||
| chr8:65663516 | A | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0107 a0001c0001t0001g0196 others(2): Show |
5 | HG01106.hp2 HG02257.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-6357A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663516 | |||||||
| chr8:65663529 | T | TA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(85): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-80-6326dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | ||||||
| chr8:65663529 | TA | T | 69 | a0001c0001t0001g0101 a0001c0001t0001g0229 a0001c0001t0001g0253 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-80-6326delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | ||||||
| chr8:65663529 | TAA | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0068 a0001c0001t0002g0069 others(3): Show |
6 | HG02109.hp2 HG03195.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-80-6327_-80-6326d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | ||||||
| chr8:65663631 | A | AT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6241dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663631 | ||||||
| chr8:65663822 | C | CT | 19 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
19 | HG02027.hp2 HG02148.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-80-6031dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663822 | ||||||
| chr8:65663822 | CT | C | 30 | a0001c0001t0001g0096 a0001c0001t0001g0130 a0001c0001t0001g0176 others(27): Show |
30 | HG00642.hp2 HG01069.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-80-6031delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663822 | ||||||
| chr8:65663913 | C | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0333 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-80-5960C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663913 | |||||||
| chr8:65663988 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-80-5885G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663988 | |||||||
| chr8:65664005 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-5868G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664005 | |||||||
| chr8:65664084 | A | G | 14 | a0001c0001t0004g0074 a0001c0001t0004g0075 a0001c0001t0004g0076 others(11): Show |
14 | HG00438.hp2 HG01099.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-80-5789A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664084 | |||||||
| chr8:65664117 | T | C | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-80-5756T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664117 | |||||||
| chr8:65664185 | C | T | 1 | a0001c0001t0004g0140 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-80-5688C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664185 | |||||||
| chr8:65664579 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-5294C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664579 | |||||||
| chr8:65664610 | G | GT | 11 | a0001c0001t0001g0080 a0001c0001t0001g0141 a0001c0001t0001g0171 others(8): Show |
11 | HG02074.hp1 HG02135.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-80-5245dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664610 | ||||||
| chr8:65664610 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-80-5263G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664610 | |||||||
| chr8:65664610 | GT | G | 15 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(12): Show |
15 | HG01069.hp1 HG01109.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-80-5245delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664610 | ||||||
| chr8:65664615 | T | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-5258T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664615 | |||||||
| chr8:65664616 | T | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
10 | HG02895.hp2 HG02897.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-80-5257T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664616 | |||||||
| chr8:65664633 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-5240A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664633 | |||||||
| chr8:65664688 | C | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-80-5185C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664688 | |||||||
| chr8:65664772 | G | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-5101G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664772 | |||||||
| chr8:65664839 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-5034T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664839 | |||||||
| chr8:65664845 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-80-5028C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664845 | |||||||
| chr8:65664878 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0307 |
2 | HG01167.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-80-4995G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664878 | |||||||
| chr8:65664911 | T | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0189 a0001c0001t0001g0223 others(40): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-80-4962T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664911 | |||||||
| chr8:65664933 | A | AT | 84 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(81): Show |
84 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-80-4919dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | ||||||
| chr8:65664933 | A | ATT | 9 | a0001c0001t0001g0087 a0001c0001t0001g0114 a0001c0001t0001g0128 others(6): Show |
9 | HG02074.hp1 HG02135.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-4920_-80-4919d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | ||||||
| chr8:65664933 | A | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(11): Show |
15 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-80-4940A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664933 | |||||||
| chr8:65664933 | AT | A | 63 | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0001g0206 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.-80-4919delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | ||||||
| chr8:65664936 | T | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-4937T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664936 | |||||||
| chr8:65665010 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-80-4863C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665010 | |||||||
| chr8:65665082 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-4791G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665082 | |||||||
| chr8:65665601 | A | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-80-4272A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665601 | |||||||
| chr8:65665639 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0012g0144 |
2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-80-4234G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665639 | |||||||
| chr8:65665914 | TA | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3957delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65665914 | ||||||
| chr8:65665930 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3943T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665930 | |||||||
| chr8:65665989 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-80-3884T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665989 | |||||||
| chr8:65666105 | T | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3768T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666105 | |||||||
| chr8:65666111 | A | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-3762A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666111 | |||||||
| chr8:65666170 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-80-3703G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666170 | |||||||
| chr8:65666295 | T | TA | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3578_-80-3577i others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666295 | |||||||
| chr8:65666526 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-3347G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666526 | |||||||
| chr8:65666879 | C | T | 1 | a0001c0001t0008g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-80-2994C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666879 | |||||||
| chr8:65666924 | T | C | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0065 others(1): Show |
4 | HG00741.hp1 HG01192.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-2949T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666924 | |||||||
| chr8:65666997 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-80-2876A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666997 | |||||||
| chr8:65667010 | C | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2863C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667010 | |||||||
| chr8:65667023 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2850C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667023 | |||||||
| chr8:65667090 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-80-2783C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667090 | |||||||
| chr8:65667107 | G | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-2766G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667107 | |||||||
| chr8:65667201 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-80-2672G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667201 | |||||||
| chr8:65667208 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2665A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667208 | |||||||
| chr8:65667215 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-80-2658G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667215 | |||||||
| chr8:65667276 | CA | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-80-2585delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667276 | ||||||
| chr8:65667346 | G | GT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0146 a0001c0001t0001g0227 others(10): Show |
13 | HG02135.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-80-2516dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667346 | ||||||
| chr8:65667346 | G | GTT | 58 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-80-2517_-80-2516d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667346 | ||||||
| chr8:65667461 | C | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-2412C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667461 | |||||||
| chr8:65667479 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0306 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-80-2394G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667479 | |||||||
| chr8:65667521 | G | A | 41 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.-80-2352G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667521 | |||||||
| chr8:65667638 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2235G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667638 | |||||||
| chr8:65667722 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2151T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667722 | |||||||
| chr8:65667726 | C | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-2147C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667726 | |||||||
| chr8:65667838 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(12): Show |
16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-80-2035T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667838 | |||||||
| chr8:65667978 | C | G | 1 | a0001c0001t0006g0342 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-80-1895C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667978 | |||||||
| chr8:65667982 | A | G | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-1891A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667982 | |||||||
| chr8:65668028 | T | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-1845T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668028 | |||||||
| chr8:65668049 | C | T | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-1824C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668049 | |||||||
| chr8:65668183 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0007g0192 |
2 | NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-80-1690T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668183 | |||||||
| chr8:65668184 | C | CT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(89): Show |
93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-80-1678dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668184 | ||||||
| chr8:65668184 | C | T | 4 | a0001c0001t0001g0274 a0001c0001t0001g0281 a0001c0001t0002g0051 others(1): Show |
4 | HG02074.hp1 NA18957.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-1689C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668184 | |||||||
| chr8:65668184 | CT | C | 14 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0249 others(11): Show |
14 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-80-1678delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668184 | ||||||
| chr8:65668323 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-80-1550G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668323 | |||||||
| chr8:65668344 | AT | A | 195 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-80-1514delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668344 | ||||||
| chr8:65668400 | T | C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-1473T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668400 | |||||||
| chr8:65668416 | G | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0195 others(1): Show |
4 | HG00438.hp1 NA18944.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-1457G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668416 | |||||||
| chr8:65668435 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0116 |
2 | HG02155.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-80-1438G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668435 | |||||||
| chr8:65668467 | CATG | C | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-1404_-80-1402d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668467 | ||||||
| chr8:65668468 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-80-1405A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668468 | |||||||
| chr8:65668477 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-1396C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668477 | |||||||
| chr8:65668525 | C | CT | 99 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0206 others(96): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-80-1331dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668525 | ||||||
| chr8:65668525 | CT | C | 7 | a0001c0001t0001g0130 a0001c0001t0001g0189 a0001c0001t0001g0229 others(4): Show |
7 | HG01167.hp1 HG02698.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-1331delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668525 | ||||||
| chr8:65668534 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-80-1339T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668534 | |||||||
| chr8:65668584 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-80-1289G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668584 | |||||||
| chr8:65668587 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-80-1286A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668587 | |||||||
| chr8:65668608 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-80-1265G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668608 | |||||||
| chr8:65668682 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-80-1191T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668682 | |||||||
| chr8:65668810 | G | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-80-1063G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668810 | |||||||
| chr8:65668823 | T | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-1050T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668823 | |||||||
| chr8:65669002 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-80-871G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669002 | |||||||
| chr8:65669064 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-809C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669064 | |||||||
| chr8:65669418 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-455A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669418 | |||||||
| chr8:65669476 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-80-397A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669476 | |||||||
| chr8:65669556 | G | GT | 8 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01952.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.-80-304dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65669556 | ||||||
| chr8:65669628 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-245C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669628 | |||||||
| chr8:65670436 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+418A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670436 | |||||||
| chr8:65670506 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66+488G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670506 | |||||||
| chr8:65670592 | T | C | 81 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(78): Show |
81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.66+574T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670592 | |||||||
| chr8:65670631 | T | G | 1 | a0001c0001t0001g0336 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.66+613T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670631 | |||||||
| chr8:65670707 | C | CT | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.66+703dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65670707 | ||||||
| chr8:65670765 | A | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(12): Show |
16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+747A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670765 | |||||||
| chr8:65670799 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(12): Show |
16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+781G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670799 | |||||||
| chr8:65671023 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+1005T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671023 | |||||||
| chr8:65671090 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66+1072G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671090 | |||||||
| chr8:65671102 | G | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+1084G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671102 | |||||||
| chr8:65671540 | T | TA | 69 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.66+1542dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65671540 | ||||||
| chr8:65671540 | TA | T | 9 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0276 others(6): Show |
9 | HG00323.hp2 HG01069.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+1542delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65671540 | ||||||
| chr8:65671561 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.66+1543G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671561 | |||||||
| chr8:65671693 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.66+1675A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671693 | |||||||
| chr8:65671783 | T | A | 51 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0083 others(48): Show |
51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+1765T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671783 | |||||||
| chr8:65671784 | G | T | 51 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0083 others(48): Show |
51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+1766G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671784 | |||||||
| chr8:65671869 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.66+1851A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671869 | |||||||
| chr8:65672033 | G | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0042 a0001c0001t0002g0043 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.66+2015G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65672033 | |||||||
| chr8:65672330 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.66+2312T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65672330 | |||||||
| chr8:65672515 | C | CT | 36 | a0001c0001t0002g0001 a0001c0001t0002g0042 a0001c0001t0002g0043 others(33): Show |
37 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.66+2508dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65672515 | ||||||
| chr8:65673311 | T | C | 79 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(76): Show |
79 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.66+3293T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673311 | |||||||
| chr8:65673331 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.66+3313C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673331 | |||||||
| chr8:65673605 | T | TA | 88 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(85): Show |
88 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.66+3601dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65673605 | ||||||
| chr8:65673675 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.66+3657G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673675 | |||||||
| chr8:65673846 | C | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3828C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673846 | |||||||
| chr8:65673920 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.66+3902A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673920 | |||||||
| chr8:65673926 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.66+3908T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673926 | |||||||
| chr8:65674212 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66+4194C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674212 | |||||||
| chr8:65674228 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.66+4210C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674228 | |||||||
| chr8:65674261 | A | C | 2 | a0001c0001t0005g0018 a0001c0001t0005g0019 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.66+4243A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674261 | |||||||
| chr8:65674303 | CT | C | 10 | a0001c0001t0001g0153 a0001c0001t0001g0167 a0001c0001t0001g0170 others(7): Show |
10 | HG01167.hp1 HG01167.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+4301delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65674303 | ||||||
| chr8:65674320 | A | T | 19 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+4302A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674320 | |||||||
| chr8:65674440 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.66+4422G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674440 | |||||||
| chr8:65675177 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.66+5159G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675177 | |||||||
| chr8:65675185 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0277 |
2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.66+5167G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675185 | |||||||
| chr8:65675207 | G | A | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+5189G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675207 | |||||||
| chr8:65675261 | CCAGCCTG others(2): Show |
C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.66+5245_66+5253del others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65675261 | ||||||
| chr8:65675288 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+5270G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675288 | |||||||
| chr8:65675322 | G | A | 1 | a0001c0001t0005g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.66+5304G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675322 | |||||||
| chr8:65675549 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.66+5531A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675549 | |||||||
| chr8:65675933 | C | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+5915C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675933 | |||||||
| chr8:65676230 | A | C | 4 | a0001c0001t0002g0039 a0001c0001t0002g0049 a0001c0001t0002g0050 others(1): Show |
4 | HG00140.hp2 HG01516.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6123A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676230 | |||||||
| chr8:65676425 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0141 a0001c0001t0001g0229 |
3 | HG01167.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67-5928G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676425 | |||||||
| chr8:65676457 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.67-5896G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676457 | |||||||
| chr8:65676458 | G | T | 1 | a0001c0001t0004g0127 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.67-5895G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676458 | |||||||
| chr8:65676463 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-5890A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676463 | |||||||
| chr8:65676520 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.67-5833C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676520 | |||||||
| chr8:65676697 | A | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0316 a0001c0001t0001g0319 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-5656A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676697 | |||||||
| chr8:65676978 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(32): Show |
36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-5375G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676978 | |||||||
| chr8:65676980 | GCA | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-5360_67-5359del others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65676980 | ||||||
| chr8:65676985 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.67-5368C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676985 | |||||||
| chr8:65677068 | C | CT | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
69 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.67-5262dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | ||||||
| chr8:65677068 | C | CTT | 7 | a0001c0001t0001g0251 a0001c0001t0001g0276 a0001c0001t0001g0291 others(4): Show |
7 | HG00733.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-5263_67-5262dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | ||||||
| chr8:65677068 | CT | C | 29 | a0001c0001t0001g0176 a0001c0001t0001g0280 a0001c0001t0001g0285 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.67-5262delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | ||||||
| chr8:65677103 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.67-5250T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677103 | |||||||
| chr8:65677104 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-5249C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677104 | |||||||
| chr8:65677105 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0195 others(1): Show |
4 | HG00438.hp1 NA18944.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5248G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677105 | |||||||
| chr8:65677215 | G | A | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-5138G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677215 | |||||||
| chr8:65677278 | C | G | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(1): Show |
4 | HG02040.hp1 NA18612.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5075C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677278 | |||||||
| chr8:65677338 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.67-5015G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677338 | |||||||
| chr8:65677384 | C | CT | 86 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(83): Show |
86 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.67-4951dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677384 | ||||||
| chr8:65677386 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-4967T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677386 | |||||||
| chr8:65677408 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-4945G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677408 | |||||||
| chr8:65677409 | G | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-4944G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677409 | |||||||
| chr8:65677536 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0292 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.67-4817C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677536 | |||||||
| chr8:65677845 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-4508G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677845 | |||||||
| chr8:65678014 | C | CA | 13 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0234 others(10): Show |
13 | HG00733.hp1 HG01074.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-4322dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65678014 | ||||||
| chr8:65678235 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.67-4118C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678235 | |||||||
| chr8:65678244 | C | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(32): Show |
36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-4109C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678244 | |||||||
| chr8:65678570 | A | G | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-3783A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678570 | |||||||
| chr8:65678594 | A | T | 11 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG01109.hp1 HG02630.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-3759A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678594 | |||||||
| chr8:65678665 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67-3688C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678665 | |||||||
| chr8:65678815 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.67-3538A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678815 | |||||||
| chr8:65678894 | A | T | 3 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67-3459A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678894 | |||||||
| chr8:65679003 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(32): Show |
36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-3350G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679003 | |||||||
| chr8:65679060 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.67-3293T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679060 | |||||||
| chr8:65679094 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-3259C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679094 | |||||||
| chr8:65679103 | A | C | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-3250A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679103 | |||||||
| chr8:65679185 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0213 |
2 | NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.67-3168A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679185 | |||||||
| chr8:65679234 | T | C | 13 | a0001c0001t0001g0142 a0001c0001t0001g0207 a0001c0001t0001g0216 others(10): Show |
13 | NA18955.hp1 NA18959.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-3119T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679234 | |||||||
| chr8:65679307 | T | G | 1 | a0001c0001t0001g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.67-3046T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679307 | |||||||
| chr8:65679435 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67-2918G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679435 | |||||||
| chr8:65679604 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-2749G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679604 | |||||||
| chr8:65679862 | T | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-2491T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679862 | |||||||
| chr8:65679868 | G | C | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-2485G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679868 | |||||||
| chr8:65679937 | C | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-2416C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679937 | |||||||
| chr8:65679960 | C | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-2393C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679960 | |||||||
| chr8:65680173 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67-2180G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680173 | |||||||
| chr8:65680184 | G | T | 1 | a0001c0001t0001g0280 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.67-2169G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680184 | |||||||
| chr8:65680310 | G | C | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-2043G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680310 | |||||||
| chr8:65680323 | T | A | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-2030T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680323 | |||||||
| chr8:65680627 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-1726G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680627 | |||||||
| chr8:65680690 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-1663G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680690 | |||||||
| chr8:65680740 | A | G | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1613A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680740 | |||||||
| chr8:65680853 | C | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.67-1500C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680853 | |||||||
| chr8:65680899 | C | CT | 112 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(109): Show |
113 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.67-1430dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | ||||||
| chr8:65680899 | C | CTT | 8 | a0001c0001t0001g0085 a0001c0001t0001g0108 a0001c0001t0001g0133 others(5): Show |
8 | HG00621.hp2 HG01934.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-1431_67-1430dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | ||||||
| chr8:65680899 | CTTTT | C | 19 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-1433_67-1430del others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | ||||||
| chr8:65680899 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.67-1439_67-1430del others(10): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | ||||||
| chr8:65680948 | C | G | 2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67-1405C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680948 | |||||||
| chr8:65681014 | G | A | 5 | a0001c0001t0001g0251 a0001c0001t0001g0255 a0001c0001t0001g0262 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1339G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681014 | |||||||
| chr8:65681157 | C | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1196C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681157 | |||||||
| chr8:65681261 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-1092A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681261 | |||||||
| chr8:65681592 | A | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-761A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681592 | |||||||
| chr8:65681671 | G | GT | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
64 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.67-666dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65681671 | ||||||
| chr8:65681671 | G | GTT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0100 a0001c0001t0001g0172 others(12): Show |
15 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-667_67-666dupTT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65681671 | ||||||
| chr8:65681677 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67-676T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681677 | |||||||
| chr8:65681814 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67-539A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681814 | |||||||
| chr8:65682049 | TATGAAAA others(4): Show |
T | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67-296_67-286delCC others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65682049 | ||||||
| chr8:65682185 | A | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-168A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65682185 | |||||||
| chr8:65682314 | A | C | 1 | a0001c0001t0009g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.67-39A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65682314 | |||||||
| chr8:65682555 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(16): Show |
20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+104A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682555 | |||||||
| chr8:65682577 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.165+126T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682577 | |||||||
| chr8:65682972 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+521T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682972 | |||||||
| chr8:65683120 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+669G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683120 | |||||||
| chr8:65683132 | C | CT | 13 | a0001c0001t0001g0175 a0001c0001t0001g0189 a0001c0001t0001g0234 others(10): Show |
13 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+700dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65683132 | ||||||
| chr8:65683132 | CT | C | 66 | a0001c0001t0001g0101 a0001c0001t0001g0222 a0001c0001t0001g0229 others(63): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.165+700delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65683132 | ||||||
| chr8:65683412 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+961G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683412 | |||||||
| chr8:65683534 | T | C | 6 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0219 others(3): Show |
6 | NA18959.hp2 NA18979.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+1083T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683534 | |||||||
| chr8:65683608 | G | T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.165+1157G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683608 | |||||||
| chr8:65683727 | T | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.165+1276T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683727 | |||||||
| chr8:65683776 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 |
3 | HG02040.hp1 NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.165+1325C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683776 | |||||||
| chr8:65683992 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.165+1541A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683992 | |||||||
| chr8:65684059 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+1608G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684059 | |||||||
| chr8:65684060 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.165+1609T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684060 | |||||||
| chr8:65684083 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.165+1632G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684083 | |||||||
| chr8:65684085 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.165+1634A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684085 | |||||||
| chr8:65684629 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.165+2178T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684629 | |||||||
| chr8:65684802 | C | T | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+2351C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684802 | |||||||
| chr8:65684879 | CT | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.165+2429delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684879 | |||||||
| chr8:65685034 | T | G | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2583T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685034 | |||||||
| chr8:65685107 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.165+2656T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685107 | |||||||
| chr8:65685247 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.165+2796T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685247 | |||||||
| chr8:65685470 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.165+3019C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685470 | |||||||
| chr8:65685671 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.165+3220G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685671 | |||||||
| chr8:65685679 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.165+3228G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685679 | |||||||
| chr8:65685796 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.165+3345A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685796 | |||||||
| chr8:65685890 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+3439C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685890 | |||||||
| chr8:65685969 | G | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+3518G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685969 | |||||||
| chr8:65686022 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165+3571A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686022 | |||||||
| chr8:65686146 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.165+3695T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686146 | |||||||
| chr8:65686253 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.165+3802C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686253 | |||||||
| chr8:65686348 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.165+3897G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686348 | |||||||
| chr8:65686400 | C | T | 22 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+3949C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686400 | |||||||
| chr8:65686457 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.165+4006A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686457 | |||||||
| chr8:65686463 | T | G | 5 | a0001c0001t0001g0251 a0001c0001t0001g0255 a0001c0001t0001g0262 others(2): Show |
5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4012T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686463 | |||||||
| chr8:65686579 | C | CA | 21 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0108 others(18): Show |
21 | HG00280.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+4149dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686579 | ||||||
| chr8:65686579 | CA | C | 68 | a0001c0001t0001g0212 a0001c0001t0001g0246 a0001c0001t0001g0252 others(65): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.165+4149delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686579 | ||||||
| chr8:65686597 | A | C | 1 | a0001c0001t0003g0030 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.165+4146A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686597 | |||||||
| chr8:65686600 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+4149A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686600 | |||||||
| chr8:65686845 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.165+4394A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686845 | |||||||
| chr8:65686845 | AC | A | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4397delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686845 | ||||||
| chr8:65686848 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.165+4397C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686848 | |||||||
| chr8:65687347 | CT | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.165+4913delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65687347 | ||||||
| chr8:65687835 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+5384C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687835 | |||||||
| chr8:65687970 | C | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+5519C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687970 | |||||||
| chr8:65687981 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165+5530T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687981 | |||||||
| chr8:65687998 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.165+5547A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687998 | |||||||
| chr8:65688000 | T | C | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+5549T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688000 | |||||||
| chr8:65688027 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.165+5576G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688027 | |||||||
| chr8:65688059 | C | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.166-5585C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688059 | |||||||
| chr8:65688098 | T | TA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0078 others(89): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.166-5528dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | ||||||
| chr8:65688098 | T | TAA | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(4): Show |
7 | HG01074.hp1 HG02622.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-5529_166-5528d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | ||||||
| chr8:65688098 | T | TAAAAA | 18 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(15): Show |
18 | HG00140.hp1 HG01168.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-5532_166-5528d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | ||||||
| chr8:65688098 | TA | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(30): Show |
34 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.166-5528delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | ||||||
| chr8:65688118 | A | C | 8 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0296 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-5526A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688118 | |||||||
| chr8:65688230 | A | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0260 others(32): Show |
36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-5414A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688230 | |||||||
| chr8:65688405 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0152 |
2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.166-5239A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688405 | |||||||
| chr8:65688451 | C | CT | 108 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.166-5178dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688451 | ||||||
| chr8:65688451 | C | CTT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
18 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-5179_166-5178d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688451 | ||||||
| chr8:65688456 | T | C | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-5188T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688456 | |||||||
| chr8:65688472 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.166-5172G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688472 | |||||||
| chr8:65688512 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-5132A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688512 | |||||||
| chr8:65688675 | A | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-4969A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688675 | |||||||
| chr8:65688719 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0001g0147 |
3 | HG02027.hp2 NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.166-4925A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688719 | |||||||
| chr8:65688725 | G | A | 5 | a0001c0001t0001g0260 a0001c0001t0001g0322 a0001c0001t0001g0329 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4919G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688725 | |||||||
| chr8:65688916 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.166-4728G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688916 | |||||||
| chr8:65689102 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-4542G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689102 | |||||||
| chr8:65689200 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.166-4444G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689200 | |||||||
| chr8:65689334 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.166-4310C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689334 | |||||||
| chr8:65689434 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-4210G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689434 | |||||||
| chr8:65689546 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-4098T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689546 | |||||||
| chr8:65689812 | AAAG | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3827_166-3825d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65689812 | ||||||
| chr8:65690111 | CAT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(17): Show |
21 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-3530_166-3529d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65690111 | ||||||
| chr8:65690278 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-3366T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690278 | |||||||
| chr8:65690367 | T | C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-3277T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690367 | |||||||
| chr8:65690374 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0189 a0001c0001t0001g0223 others(40): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.166-3270C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690374 | |||||||
| chr8:65690461 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3183G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690461 | |||||||
| chr8:65690551 | T | C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-3093T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690551 | |||||||
| chr8:65690560 | G | GT | 71 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.166-3077dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65690560 | ||||||
| chr8:65690599 | C | T | 12 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(9): Show |
12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-3045C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690599 | |||||||
| chr8:65690626 | A | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3018A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690626 | |||||||
| chr8:65690735 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0229 |
2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.166-2909T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690735 | |||||||
| chr8:65690837 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-2807C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690837 | |||||||
| chr8:65691362 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0208 |
2 | HG01496.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.166-2282A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691362 | |||||||
| chr8:65691505 | C | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-2139C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691505 | |||||||
| chr8:65691640 | A | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-2004A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691640 | |||||||
| chr8:65691658 | G | GT | 8 | a0001c0001t0001g0095 a0001c0001t0001g0188 a0001c0001t0001g0216 others(5): Show |
8 | HG01123.hp1 HG01346.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-1977dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65691658 | ||||||
| chr8:65691725 | C | T | 13 | a0001c0001t0001g0142 a0001c0001t0001g0207 a0001c0001t0001g0216 others(10): Show |
13 | NA18955.hp1 NA18959.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1919C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691725 | |||||||
| chr8:65692012 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-1632T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692012 | |||||||
| chr8:65692347 | T | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0255 |
2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.166-1297T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692347 | |||||||
| chr8:65692355 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0173 a0001c0001t0001g0174 others(42): Show |
46 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.166-1289T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692355 | |||||||
| chr8:65692423 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.166-1221C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692423 | |||||||
| chr8:65692716 | CTGTT | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-923_166-920del others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65692716 | ||||||
| chr8:65692793 | T | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.166-851T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692793 | |||||||
| chr8:65692892 | C | CT | 8 | a0001c0001t0001g0108 a0001c0001t0001g0151 a0001c0001t0001g0226 others(5): Show |
8 | HG01258.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-737dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65692892 | ||||||
| chr8:65692966 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-678G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692966 | |||||||
| chr8:65693104 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-540T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693104 | |||||||
| chr8:65693256 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-388C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693256 | |||||||
| chr8:65693315 | C | T | 1 | a0001c0001t0004g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-329C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693315 | |||||||
| chr8:65693316 | G | A | 62 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.166-328G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693316 | |||||||
| chr8:65693356 | AG | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-287delG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693356 | |||||||
| chr8:65693401 | C | CA | 10 | a0001c0001t0001g0179 a0001c0001t0002g0043 a0001c0001t0002g0047 others(7): Show |
10 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-230dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65693401 | ||||||
| chr8:65693401 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.166-243C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693401 | |||||||
| chr8:65693533 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-111A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693533 | |||||||
| chr8:65693629 | A | G | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-15A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693629 | |||||||
| chr8:65693827 | G | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+68G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65693827 | |||||||
| chr8:65693924 | A | G | 1 | a0001c0001t0011g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.281+165A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65693924 | |||||||
| chr8:65694072 | C | CT | 73 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0094 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.281+334dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65694072 | ||||||
| chr8:65694072 | CT | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(24): Show |
27 | HG01109.hp1 HG01255.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.281+334delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65694072 | ||||||
| chr8:65694184 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.281+425C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694184 | |||||||
| chr8:65694321 | C | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0333 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.281+562C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694321 | |||||||
| chr8:65694434 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+675G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694434 | |||||||
| chr8:65694534 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281+775C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694534 | |||||||
| chr8:65694765 | A | C | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281+1006A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694765 | |||||||
| chr8:65694984 | G | A | 92 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+1225G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694984 | |||||||
| chr8:65695006 | A | C | 1 | a0001c0001t0006g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.281+1247A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695006 | |||||||
| chr8:65695059 | T | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0141 a0001c0001t0001g0229 others(1): Show |
4 | HG01167.hp1 HG02109.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+1300T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695059 | |||||||
| chr8:65695209 | G | A | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+1450G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695209 | |||||||
| chr8:65695312 | T | C | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+1553T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695312 | |||||||
| chr8:65695347 | A | AT | 31 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.281+1599dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65695347 | ||||||
| chr8:65695495 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.281+1736T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695495 | |||||||
| chr8:65695532 | T | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+1773T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695532 | |||||||
| chr8:65695830 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.281+2071T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695830 | |||||||
| chr8:65695867 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.281+2108A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695867 | |||||||
| chr8:65695874 | G | A | 27 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0153 others(24): Show |
27 | HG01123.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.281+2115G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695874 | |||||||
| chr8:65695970 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+2211A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695970 | |||||||
| chr8:65696265 | C | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+2506C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696265 | |||||||
| chr8:65696413 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0273 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.281+2654C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696413 | |||||||
| chr8:65696618 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.281+2859C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696618 | |||||||
| chr8:65696716 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281+2957G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696716 | |||||||
| chr8:65696746 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.281+2987C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696746 | |||||||
| chr8:65696824 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.281+3065C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696824 | |||||||
| chr8:65696829 | T | C | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.281+3070T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696829 | |||||||
| chr8:65696912 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281+3153C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696912 | |||||||
| chr8:65696938 | A | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3179A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696938 | |||||||
| chr8:65696984 | C | CT | 130 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(127): Show |
131 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.281+3243dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65696984 | ||||||
| chr8:65697096 | T | C | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3337T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697096 | |||||||
| chr8:65697129 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0308 a0001c0001t0001g0309 |
3 | HG02451.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.281+3370C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697129 | |||||||
| chr8:65697156 | T | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+3397T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697156 | |||||||
| chr8:65697286 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.281+3527A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697286 | |||||||
| chr8:65697314 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.281+3555A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697314 | |||||||
| chr8:65697341 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.281+3582C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697341 | |||||||
| chr8:65697707 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281+3948G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697707 | |||||||
| chr8:65697740 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3981G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697740 | |||||||
| chr8:65697750 | A | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+3991A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697750 | |||||||
| chr8:65697788 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281+4029A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697788 | |||||||
| chr8:65697839 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281+4080C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697839 | |||||||
| chr8:65697999 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281+4240G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697999 | |||||||
| chr8:65698115 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.281+4356G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698115 | |||||||
| chr8:65698142 | A | T | 5 | a0001c0001t0005g0014 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02965.hp1 HG03540.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+4383A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698142 | |||||||
| chr8:65698154 | C | CT | 65 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0080 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.281+4408dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65698154 | ||||||
| chr8:65698251 | C | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+4492C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698251 | |||||||
| chr8:65698253 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+4494A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698253 | |||||||
| chr8:65698382 | C | T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.281+4623C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698382 | |||||||
| chr8:65698491 | C | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.281+4732C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698491 | |||||||
| chr8:65698571 | G | A | 100 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.281+4812G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698571 | |||||||
| chr8:65698594 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.281+4835A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698594 | |||||||
| chr8:65698732 | C | CT | 30 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 others(27): Show |
30 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.281+4986dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65698732 | ||||||
| chr8:65698792 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281+5033G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698792 | |||||||
| chr8:65698885 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281+5126C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698885 | |||||||
| chr8:65698965 | G | A | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+5206G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698965 | |||||||
| chr8:65699182 | C | T | 92 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+5423C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699182 | |||||||
| chr8:65699307 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.282-5387G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699307 | |||||||
| chr8:65699355 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-5339C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699355 | |||||||
| chr8:65699381 | A | G | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-5313A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699381 | |||||||
| chr8:65699465 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.282-5229A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699465 | |||||||
| chr8:65699467 | A | C | 1 | a0001c0001t0004g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.282-5227A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699467 | |||||||
| chr8:65699572 | C | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-5122C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699572 | |||||||
| chr8:65699749 | C | G | 2 | a0001c0001t0001g0325 a0001c0001t0001g0327 |
2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.282-4945C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699749 | |||||||
| chr8:65699779 | A | G | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-4915A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699779 | |||||||
| chr8:65700175 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0229 |
2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.282-4519A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700175 | |||||||
| chr8:65700225 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.282-4469C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700225 | |||||||
| chr8:65700272 | G | A | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.282-4422G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700272 | |||||||
| chr8:65700335 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
11 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-4359A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700335 | |||||||
| chr8:65700349 | TA | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0208 a0001c0001t0001g0270 others(3): Show |
6 | HG01070.hp1 HG01255.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-4328delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65700349 | ||||||
| chr8:65700366 | AG | A | 12 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0003g0016 others(9): Show |
12 | HG00140.hp1 HG02647.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-4327delG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700366 | |||||||
| chr8:65700367 | G | A | 52 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0043 others(49): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.282-4327G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700367 | |||||||
| chr8:65700369 | A | G | 1 | a0001c0001t0011g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.282-4325A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700369 | |||||||
| chr8:65700373 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(16): Show |
20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.282-4321A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700373 | |||||||
| chr8:65700451 | G | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0023 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-4243G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700451 | |||||||
| chr8:65700754 | T | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0173 a0001c0001t0001g0174 others(34): Show |
38 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.282-3940T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700754 | |||||||
| chr8:65701032 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.282-3662G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701032 | |||||||
| chr8:65701107 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.282-3587A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701107 | |||||||
| chr8:65701289 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0055 |
2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.282-3405G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701289 | |||||||
| chr8:65701710 | A | C | 1 | a0001c0001t0001g0336 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.282-2984A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701710 | |||||||
| chr8:65701726 | A | G | 77 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(74): Show |
77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.282-2968A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701726 | |||||||
| chr8:65702152 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-2542C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702152 | |||||||
| chr8:65702263 | TTTTCTTT others(6): Show |
T | 31 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.282-2418_282-2406d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702263 | ||||||
| chr8:65702297 | CT | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(91): Show |
95 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.282-2377delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702297 | ||||||
| chr8:65702297 | CTT | C | 24 | a0001c0001t0001g0222 a0001c0001t0001g0249 a0001c0001t0001g0250 others(21): Show |
24 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.282-2378_282-2377d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702297 | ||||||
| chr8:65702301 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282-2393T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702301 | |||||||
| chr8:65702302 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0104 |
2 | HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282-2392T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702302 | |||||||
| chr8:65702484 | G | C | 32 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.282-2210G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702484 | |||||||
| chr8:65702560 | C | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(280): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.282-2134C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702560 | |||||||
| chr8:65702602 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.282-2092T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702602 | |||||||
| chr8:65702704 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1990G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702704 | |||||||
| chr8:65702793 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.282-1901T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702793 | |||||||
| chr8:65702823 | A | AT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0042 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.282-1871_282-1870i others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702823 | |||||||
| chr8:65702849 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0167 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-1845T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702849 | |||||||
| chr8:65702908 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.282-1786A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702908 | |||||||
| chr8:65703062 | A | AGTTAACT others(8): Show |
1 | a0001c0001t0001g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.282-1631_282-1617d others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703062 | ||||||
| chr8:65703077 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.282-1617G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703077 | |||||||
| chr8:65703090 | G | GA | 6 | a0001c0001t0001g0254 a0001c0001t0001g0266 a0001c0001t0001g0299 others(3): Show |
6 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-1591dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703090 | ||||||
| chr8:65703235 | A | G | 8 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-1459A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703235 | |||||||
| chr8:65703257 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.282-1437G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703257 | |||||||
| chr8:65703380 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.282-1314T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703380 | |||||||
| chr8:65703403 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282-1291A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703403 | |||||||
| chr8:65703419 | G | GT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0090 others(43): Show |
47 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.282-1243dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | G | GTT | 17 | a0001c0001t0001g0088 a0001c0001t0001g0143 a0001c0001t0001g0155 others(14): Show |
17 | HG01106.hp1 HG01168.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.282-1244_282-1243d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | G | GTTT | 14 | a0001c0001t0001g0148 a0001c0001t0001g0189 a0001c0001t0001g0223 others(11): Show |
14 | HG00323.hp2 HG01169.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.282-1245_282-1243d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GT | G | 13 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0099 others(10): Show |
13 | HG01346.hp1 HG02109.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.282-1243delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTT | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0096 others(22): Show |
26 | HG01099.hp2 HG01168.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.282-1244_282-1243d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTT | G | 33 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.282-1245_282-1243d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTT | G | 84 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.282-1246_282-1243d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTT | G | 8 | a0001c0001t0002g0043 a0001c0001t0005g0014 a0001c0001t0005g0015 others(5): Show |
8 | HG01943.hp1 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-1247_282-1243d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.282-1253_282-1243d others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0325 a0001c0001t0001g0327 |
3 | HG00639.hp2 HG01934.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.282-1254_282-1243d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.282-1255_282-1243d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.282-1259_282-1243d others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703419 | GTTTTTTT others(11): Show |
G | 4 | a0001c0001t0001g0251 a0001c0001t0001g0262 a0001c0001t0001g0303 others(1): Show |
4 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-1260_282-1243d others(20): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | ||||||
| chr8:65703427 | T | TTG | 9 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-1266_282-1265i others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703427 | ||||||
| chr8:65703437 | T | G | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.282-1257T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703437 | |||||||
| chr8:65703509 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0288 a0001c0001t0001g0316 others(6): Show |
10 | HG00323.hp2 HG00639.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.282-1185C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703509 | |||||||
| chr8:65703622 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282-1072C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703622 | |||||||
| chr8:65703701 | C | T | 6 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-993C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703701 | |||||||
| chr8:65703766 | T | C | 71 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.282-928T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703766 | |||||||
| chr8:65703783 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.282-911A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703783 | |||||||
| chr8:65703861 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282-833C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703861 | |||||||
| chr8:65703941 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.282-753C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703941 | |||||||
| chr8:65704231 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.282-463A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704231 | |||||||
| chr8:65704320 | T | G | 1 | a0001c0001t0003g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.282-374T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704320 | |||||||
| chr8:65704400 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.282-294G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704400 | |||||||
| chr8:65704671 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.282-23C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704671 | |||||||
| chr8:65705000 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517+71A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705000 | |||||||
| chr8:65705121 | C | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.517+192C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705121 | |||||||
| chr8:65705149 | C | G | 82 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.517+220C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705149 | |||||||
| chr8:65705301 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517+372C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705301 | |||||||
| chr8:65705302 | G | A | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0005g0018 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+373G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705302 | |||||||
| chr8:65705355 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.517+426G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705355 | |||||||
| chr8:65705430 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.517+501C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705430 | |||||||
| chr8:65705627 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.517+698G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705627 | |||||||
| chr8:65705690 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517+761C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705690 | |||||||
| chr8:65705918 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+989G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705918 | |||||||
| chr8:65706192 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.518-818T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706192 | |||||||
| chr8:65706268 | A | ATAATTTT others(51): Show |
1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.518-741_518-684dup others(58): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 65706268 | ||||||
| chr8:65706325 | A | G | 8 | a0001c0001t0001g0189 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-685A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706325 | |||||||
| chr8:65706353 | A | G | 5 | a0001c0001t0002g0051 a0001c0001t0002g0054 a0001c0001t0002g0057 others(2): Show |
5 | NA18989.hp2 NA18997.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-657A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706353 | |||||||
| chr8:65706485 | C | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.518-525C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706485 | |||||||
| chr8:65706581 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA18993.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.518-429G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706581 | |||||||
| chr8:65707461 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.764+205T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707461 | |||||||
| chr8:65707530 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.764+274A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707530 | |||||||
| chr8:65707536 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0094 a0001c0001t0001g0095 others(12): Show |
16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.764+280A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707536 | |||||||
| chr8:65707594 | CTATTTGC others(50): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-248_765-192del others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707594 | |||||||
| chr8:65707659 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-184T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707659 | |||||||
| chr8:65707664 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-179T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707664 | |||||||
| chr8:65707748 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.765-95G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707748 | |||||||
| chr8:65708061 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.933+50T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708061 | |||||||
| chr8:65708124 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
60 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.933+113G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708124 | |||||||
| chr8:65708391 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.933+380G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708391 | |||||||
| chr8:65708613 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.934-363C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708613 | |||||||
| chr8:65708918 | C | T | 3 | a0001c0001t0006g0340 a0001c0001t0006g0341 a0001c0001t0006g0342 |
3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.934-58C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708918 | |||||||
| chr8:65708919 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.934-57G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708919 |