Item | Value |
---|---|
geneid | 441024 |
ensemblid | ENSG00000163738.19 |
hgncid | 31865 |
symbol | MTHFD2L |
name | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like |
refseq_nuc | NM_001144978.3 |
refseq_prot | NP_001138450.1 |
ensembl_nuc | ENST00000325278.7 |
ensembl_prot | ENSP00000321984.7 |
mane_status | MANE Select |
chr | chr4 |
start | 74158118 |
end | 74303099 |
strand | + |
ver | v1.2 |
region | chr4:74158118-74303099 |
region5000 | chr4:74153118-74308099 |
regionname0 | MTHFD2L_chr4_74158118_74303099 |
regionname5000 | MTHFD2L_chr4_74153118_74308099 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 347 | 199 | 74 | 32 | 71 | 2 | 18 | 49 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | MTVPV others(342): Show |
chr4 | 74153118 | 74308099 |
a0002 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | MTVPV others(342): Show |
chr4 | 74153118 | 74308099 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1041 | 196 | 72 | 32 | 70 | 2 | 18 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | ATGAC others(1036): Show |
chr4 | 74153118 | 74308099 | ||
a0001c0003 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | ATGAC others(1036): Show |
chr4 | 74153118 | 74308099 | ||
a0001c0004 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | ATGAC others(1036): Show |
chr4 | 74153118 | 74308099 | ||
a0001c0005 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | ATGAC others(1036): Show |
chr4 | 74153118 | 74308099 | ||
a0002c0002 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | ATGAC others(1036): Show |
chr4 | 74153118 | 74308099 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2355 | 102 | 26 | 23 | 41 | 1 | 9 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0002 | 0/0 | 2355 | 45 | 28 | 4 | 9 | 0 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0003 | 0/0 | 2355 | 43 | 13 | 5 | 20 | 1 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0004 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0005 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0006 | 0/0 | 2355 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0001t0007 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0003t0004 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0004t0001 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0001c0005t0001 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
a0002c0002t0001 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | GGAAG others(2350): Show |
chr4 | 74153118 | 74308099 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0003 | g0111 | EUR | FIN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CDX | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0103 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18975 | hp1 | a0001 | c0005 | t0001 | g0099 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | USA | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0070 | REF | REF | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0191 | REF | REF | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74201285 | T | A | 1 | a0002 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.627T>A | p.Asn209Lys | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/8 | 648/2355 | 627/1044 | 209/347 | chr4 | 74201285 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74158171 | C | G | 1 | a0001c0005 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.33C>G | p.Leu11Leu | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/8 | 54/2355 | 33/1044 | 11/347 | chr4 | 74158171 | |||
chr4:74174533 | C | T | 1 | a0001c0004 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.171C>T | p.Thr57Thr | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/8 | 192/2355 | 171/1044 | 57/347 | chr4 | 74174533 | |||
chr4:74281501 | C | T | 1 | a0001c0003 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.882C>T | p.His294His | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/8 | 903/2355 | 882/1044 | 294/347 | chr4 | 74281501 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74301815 | A | G | 2 | a0001c0001t0004 a0001c0003t0004 |
3 | HG02615.hp2 HG03516.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 6 | chr4 | 74301815 | ||||||
chr4:74302006 | C | T | 1 | a0001c0001t0007 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 197 | chr4 | 74302006 | ||||||
chr4:74302056 | A | G | 1 | a0001c0001t0006 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 247 | chr4 | 74302056 | ||||||
chr4:74302458 | C | T | 2 | a0001c0001t0003 a0001c0001t0006 |
44 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*649C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 649 | chr4 | 74302458 | ||||||
chr4:74302854 | T | C | 2 | a0001c0001t0002 a0001c0001t0007 |
46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 1045 | chr4 | 74302854 | ||||||
chr4:74303068 | A | G | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(2): Show |
92 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1259A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 1259 | chr4 | 74303068 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74158577 | A | G | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.143+296A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158577 | |||||||
chr4:74158626 | T | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+345T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158626 | |||||||
chr4:74158748 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143+467T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158748 | |||||||
chr4:74158755 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143+474A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158755 | |||||||
chr4:74158805 | C | T | 5 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0195 others(2): Show |
5 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+524C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158805 | |||||||
chr4:74158906 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.143+625G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158906 | |||||||
chr4:74159244 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.143+963A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159244 | |||||||
chr4:74159269 | A | G | 7 | a0001c0001t0002g0177 a0001c0001t0003g0171 a0001c0001t0003g0172 others(4): Show |
7 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.143+988A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159269 | |||||||
chr4:74159411 | A | G | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 |
3 | NA18968.hp2 NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.143+1130A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159411 | |||||||
chr4:74159497 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143+1216G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159497 | |||||||
chr4:74159642 | G | T | 5 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 others(2): Show |
5 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+1361G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159642 | |||||||
chr4:74159652 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.143+1371C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159652 | |||||||
chr4:74159676 | C | G | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.143+1395C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159676 | |||||||
chr4:74159767 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.143+1486C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159767 | |||||||
chr4:74159880 | G | A | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.143+1599G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159880 | |||||||
chr4:74159917 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.143+1636G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159917 | |||||||
chr4:74160170 | C | G | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.143+1889C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160170 | |||||||
chr4:74160192 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.143+1911G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160192 | |||||||
chr4:74160351 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+2070G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160351 | |||||||
chr4:74160814 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG01070.hp2 HG01071.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.143+2533G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160814 | |||||||
chr4:74161170 | T | A | 2 | a0001c0001t0003g0011 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.143+2889T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161170 | |||||||
chr4:74161241 | C | T | 14 | a0001c0001t0001g0193 a0001c0001t0002g0008 a0001c0001t0002g0009 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.143+2960C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161241 | |||||||
chr4:74161297 | A | C | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143+3016A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161297 | |||||||
chr4:74161506 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.143+3225T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161506 | |||||||
chr4:74161532 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.143+3251G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161532 | |||||||
chr4:74162216 | CTG | C | 2 | a0001c0001t0003g0011 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.143+3939_143+3940d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74162216 | ||||||
chr4:74162370 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.143+4089A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162370 | |||||||
chr4:74162475 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.143+4194G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162475 | |||||||
chr4:74162505 | CT | C | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(67): Show |
70 | HG00408.hp1 HG00438.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.143+4244delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74162505 | ||||||
chr4:74162678 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.143+4397C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162678 | |||||||
chr4:74163075 | AT | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+4805delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | ||||||
chr4:74163075 | ATT | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
80 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(77): Show |
intron_variant | MODIFIER | c.143+4804_143+4805d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | ||||||
chr4:74163075 | ATTT | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0061 others(101): Show |
105 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.143+4803_143+4805d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | ||||||
chr4:74163098 | G | A | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143+4817G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163098 | |||||||
chr4:74163154 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.143+4873G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163154 | |||||||
chr4:74163254 | T | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.143+4973T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163254 | |||||||
chr4:74163317 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143+5036A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163317 | |||||||
chr4:74163378 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.143+5097G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163378 | |||||||
chr4:74163411 | C | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143+5130C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163411 | |||||||
chr4:74163744 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.143+5463T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163744 | |||||||
chr4:74163842 | A | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.143+5561A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163842 | |||||||
chr4:74163897 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0061 others(101): Show |
105 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.143+5616G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163897 | |||||||
chr4:74164065 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0149 a0001c0001t0001g0150 others(4): Show |
7 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.143+5784C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164065 | |||||||
chr4:74164092 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.143+5811C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164092 | |||||||
chr4:74164122 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+5841C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164122 | |||||||
chr4:74164166 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5885A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164166 | |||||||
chr4:74164167 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5886T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164167 | |||||||
chr4:74164171 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5890T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164171 | |||||||
chr4:74164331 | T | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0003g0167 |
3 | HG01243.hp2 HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.143+6050T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164331 | |||||||
chr4:74164802 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143+6521C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164802 | |||||||
chr4:74164914 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.143+6633A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164914 | |||||||
chr4:74165077 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143+6796G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165077 | |||||||
chr4:74165360 | CTTTG | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.143+7083_143+7086d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74165360 | ||||||
chr4:74165364 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143+7083G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165364 | |||||||
chr4:74165443 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143+7162C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165443 | |||||||
chr4:74165494 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.143+7213A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165494 | |||||||
chr4:74165524 | A | C | 72 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
72 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.143+7243A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165524 | |||||||
chr4:74165546 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.143+7265C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165546 | |||||||
chr4:74165784 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143+7503A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165784 | |||||||
chr4:74165951 | ATAGTT | A | 72 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
72 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.143+7673_143+7677d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74165951 | ||||||
chr4:74166077 | A | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+7796A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166077 | |||||||
chr4:74166412 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.144-8094A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166412 | |||||||
chr4:74166443 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.144-8063A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166443 | |||||||
chr4:74166679 | A | G | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-7827A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166679 | |||||||
chr4:74166852 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.144-7654C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166852 | |||||||
chr4:74166969 | G | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-7537G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166969 | |||||||
chr4:74167272 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.144-7234T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167272 | |||||||
chr4:74167398 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.144-7108C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167398 | |||||||
chr4:74167636 | G | T | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-6870G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167636 | |||||||
chr4:74167911 | T | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0029 others(104): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.144-6595T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167911 | |||||||
chr4:74168006 | C | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
11 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-6500C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168006 | |||||||
chr4:74168029 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.144-6477C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168029 | |||||||
chr4:74168034 | GT | G | 18 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-6469delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74168034 | ||||||
chr4:74168068 | C | G | 107 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0029 others(104): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.144-6438C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168068 | |||||||
chr4:74168101 | C | T | 2 | a0001c0001t0002g0165 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.144-6405C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168101 | |||||||
chr4:74168161 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-6345T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168161 | |||||||
chr4:74168421 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.144-6085G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168421 | |||||||
chr4:74168952 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.144-5554A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168952 | |||||||
chr4:74169341 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.144-5165G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169341 | |||||||
chr4:74169382 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0147 |
3 | NA18945.hp2 NA18964.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.144-5124C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169382 | |||||||
chr4:74169435 | T | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-5071T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169435 | |||||||
chr4:74169464 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(111): Show |
115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.144-5042C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169464 | |||||||
chr4:74169497 | G | A | 62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-5009G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169497 | |||||||
chr4:74169572 | A | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-4934A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169572 | |||||||
chr4:74169654 | A | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0053 others(1): Show |
4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-4852A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169654 | |||||||
chr4:74169659 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.144-4847C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169659 | |||||||
chr4:74169808 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.144-4698A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169808 | |||||||
chr4:74169963 | A | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-4543A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169963 | |||||||
chr4:74170009 | C | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.144-4497C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170009 | |||||||
chr4:74170072 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 |
3 | HG01884.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.144-4434A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170072 | |||||||
chr4:74170327 | A | G | 99 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(96): Show |
99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.144-4179A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170327 | |||||||
chr4:74170329 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.144-4177T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170329 | |||||||
chr4:74170341 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(111): Show |
115 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.144-4165C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170341 | |||||||
chr4:74170374 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.144-4132T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170374 | |||||||
chr4:74170688 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-3818G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170688 | |||||||
chr4:74170742 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.144-3764C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170742 | |||||||
chr4:74170816 | A | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-3690A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170816 | |||||||
chr4:74170965 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-3541T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170965 | |||||||
chr4:74170990 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.144-3516A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170990 | |||||||
chr4:74171004 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.144-3502G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171004 | |||||||
chr4:74171026 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.144-3480C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171026 | |||||||
chr4:74171243 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.144-3263G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171243 | |||||||
chr4:74171263 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.144-3243G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171263 | |||||||
chr4:74171449 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.144-3057G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171449 | |||||||
chr4:74171667 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0149 a0001c0001t0001g0150 others(4): Show |
7 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-2839G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171667 | |||||||
chr4:74171798 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-2708C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171798 | |||||||
chr4:74171798 | C | G | 111 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.144-2708C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171798 | |||||||
chr4:74171909 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.144-2597G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171909 | |||||||
chr4:74171937 | TAAAC | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-2565_144-2562d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74171937 | ||||||
chr4:74172129 | G | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2377G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172129 | |||||||
chr4:74172150 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-2356G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172150 | |||||||
chr4:74172443 | TAATG | T | 14 | a0001c0001t0001g0144 a0001c0001t0001g0193 a0001c0001t0002g0137 others(11): Show |
14 | HG01496.hp2 HG02258.hp2 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-2060_144-2057d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74172443 | ||||||
chr4:74172475 | T | C | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.144-2031T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172475 | |||||||
chr4:74172524 | G | T | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.144-1982G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172524 | |||||||
chr4:74172746 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.144-1760T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172746 | |||||||
chr4:74173010 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.144-1496G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173010 | |||||||
chr4:74173092 | T | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.144-1414T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173092 | |||||||
chr4:74173186 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-1320A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173186 | |||||||
chr4:74173227 | G | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1279G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173227 | |||||||
chr4:74173326 | C | A | 62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-1180C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173326 | |||||||
chr4:74173562 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.144-944A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173562 | |||||||
chr4:74173722 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-784A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173722 | |||||||
chr4:74173742 | A | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-764A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173742 | |||||||
chr4:74173918 | G | A | 18 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-588G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173918 | |||||||
chr4:74173933 | T | C | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.144-573T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173933 | |||||||
chr4:74174266 | A | T | 6 | a0001c0001t0001g0193 a0001c0001t0002g0137 a0001c0001t0002g0194 others(3): Show |
6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-240A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74174266 | |||||||
chr4:74174716 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.328+26A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174716 | |||||||
chr4:74174750 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.328+60T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174750 | |||||||
chr4:74174979 | G | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.328+289G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174979 | |||||||
chr4:74175012 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-269T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175012 | |||||||
chr4:74175061 | T | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.329-220T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175061 | |||||||
chr4:74175146 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.329-135A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175146 | |||||||
chr4:74175227 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.329-54T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175227 | |||||||
chr4:74175743 | C | T | 18 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.451+340C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74175743 | |||||||
chr4:74176232 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451+829A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176232 | |||||||
chr4:74176336 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.451+933T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176336 | |||||||
chr4:74176352 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.451+949C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176352 | |||||||
chr4:74176484 | T | C | 2 | a0001c0001t0001g0075 a0002c0002t0001g0076 |
2 | NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.451+1081T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176484 | |||||||
chr4:74176554 | G | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+1151G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176554 | |||||||
chr4:74176867 | G | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+1464G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176867 | |||||||
chr4:74177372 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.451+1969G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177372 | |||||||
chr4:74177382 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+1979C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177382 | |||||||
chr4:74177404 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0002g0131 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.451+2001A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177404 | |||||||
chr4:74177427 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.451+2024A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177427 | |||||||
chr4:74177518 | A | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+2115A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177518 | |||||||
chr4:74177643 | G | A | 34 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
34 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.451+2240G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177643 | |||||||
chr4:74177661 | T | C | 44 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(41): Show |
44 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.451+2258T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177661 | |||||||
chr4:74177809 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0007g0055 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.451+2406C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177809 | |||||||
chr4:74177910 | A | G | 6 | a0001c0001t0001g0193 a0001c0001t0002g0137 a0001c0001t0002g0194 others(3): Show |
6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+2507A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177910 | |||||||
chr4:74178058 | CAT | C | 101 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(98): Show |
101 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.451+2657_451+2658d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74178058 | ||||||
chr4:74178713 | A | G | 1 | a0001c0001t0003g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451+3310A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178713 | |||||||
chr4:74178894 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.451+3491G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178894 | |||||||
chr4:74178941 | C | G | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.451+3538C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178941 | |||||||
chr4:74178972 | G | A | 42 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(39): Show |
42 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.451+3569G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178972 | |||||||
chr4:74179543 | G | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0050 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451+4140G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179543 | |||||||
chr4:74179588 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+4185C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179588 | |||||||
chr4:74179645 | CT | C | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+4246delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74179645 | ||||||
chr4:74179734 | C | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451+4331C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179734 | |||||||
chr4:74179950 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+4547C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179950 | |||||||
chr4:74180109 | G | A | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+4706G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180109 | |||||||
chr4:74180217 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+4814A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180217 | |||||||
chr4:74180296 | A | G | 6 | a0001c0001t0001g0193 a0001c0001t0002g0137 a0001c0001t0002g0194 others(3): Show |
6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+4893A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180296 | |||||||
chr4:74180354 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.451+4951C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180354 | |||||||
chr4:74180500 | G | C | 2 | a0001c0001t0003g0041 a0001c0001t0003g0058 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.451+5097G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180500 | |||||||
chr4:74180593 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.451+5190A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180593 | |||||||
chr4:74180620 | T | C | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.451+5217T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180620 | |||||||
chr4:74180655 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+5252A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180655 | |||||||
chr4:74180904 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.451+5501T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180904 | |||||||
chr4:74180925 | A | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+5522A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180925 | |||||||
chr4:74180930 | A | T | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5527A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180930 | |||||||
chr4:74180931 | T | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5528T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180931 | |||||||
chr4:74181036 | A | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+5633A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181036 | |||||||
chr4:74181087 | A | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+5684A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181087 | |||||||
chr4:74181149 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0003g0148 others(1): Show |
4 | HG00597.hp1 HG00621.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+5746T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181149 | |||||||
chr4:74181403 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.451+6000C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181403 | |||||||
chr4:74181414 | A | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+6011A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181414 | |||||||
chr4:74181434 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0058 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.451+6031G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181434 | |||||||
chr4:74181527 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6124C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181527 | |||||||
chr4:74181659 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.451+6256T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181659 | |||||||
chr4:74182132 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6729C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182132 | |||||||
chr4:74182138 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+6735G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182138 | |||||||
chr4:74182311 | C | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+6908C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182311 | |||||||
chr4:74182471 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.451+7068T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182471 | |||||||
chr4:74182561 | C | A | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 |
3 | NA18968.hp2 NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.451+7158C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182561 | |||||||
chr4:74182675 | C | T | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+7272C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182675 | |||||||
chr4:74182719 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.451+7316G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182719 | |||||||
chr4:74182738 | G | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+7335G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182738 | |||||||
chr4:74182774 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451+7371A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182774 | |||||||
chr4:74183253 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+7850T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183253 | |||||||
chr4:74183385 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.451+7982C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183385 | |||||||
chr4:74183386 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+7983G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183386 | |||||||
chr4:74183415 | G | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+8012G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183415 | |||||||
chr4:74183526 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451+8123C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183526 | |||||||
chr4:74183812 | GTTCTTA | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.451+8418_451+8423d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74183812 | ||||||
chr4:74183962 | C | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.451+8559C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183962 | |||||||
chr4:74184046 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.451+8643C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184046 | |||||||
chr4:74184296 | A | C | 22 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0048 others(19): Show |
22 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.451+8893A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184296 | |||||||
chr4:74184308 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451+8905G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184308 | |||||||
chr4:74184966 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.451+9563G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184966 | |||||||
chr4:74185151 | C | CA | 32 | a0001c0001t0001g0029 a0001c0001t0001g0079 a0001c0001t0001g0080 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.451+9776dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAA | 7 | a0001c0001t0001g0100 a0001c0001t0001g0156 a0001c0001t0002g0002 others(4): Show |
7 | HG01243.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+9775_451+9776d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAA | 16 | a0001c0001t0001g0048 a0001c0001t0002g0050 a0001c0001t0002g0154 others(13): Show |
16 | HG02040.hp2 HG02165.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+9773_451+9776d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAA | 15 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0049 others(12): Show |
15 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+9772_451+9776d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(4): Show |
7 | HG01169.hp1 HG01891.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+9771_451+9776d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+9768_451+9776d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0197 others(1): Show |
4 | HG01243.hp2 HG03486.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+9767_451+9776d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0163 a0001c0001t0003g0026 a0001c0001t0005g0141 |
3 | HG03486.hp1 HG04184.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+9766_451+9776d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+9765_451+9776d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185151 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451+9763_451+9776d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | ||||||
chr4:74185180 | T | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
57 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.451+9777T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185180 | |||||||
chr4:74185543 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+10140A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185543 | |||||||
chr4:74185585 | T | C | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+10182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185585 | |||||||
chr4:74185673 | TAAATG | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.451+10276_451+1028 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185673 | ||||||
chr4:74185898 | C | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+10495C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185898 | |||||||
chr4:74186104 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.451+10701A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186104 | |||||||
chr4:74186142 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.451+10739A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186142 | |||||||
chr4:74186438 | G | GA | 19 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0098 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+11056dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | ||||||
chr4:74186438 | G | GAA | 89 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0062 others(86): Show |
89 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.451+11055_451+1105 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | ||||||
chr4:74186438 | G | GAAA | 21 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(18): Show |
21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.451+11054_451+1105 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | ||||||
chr4:74186438 | GA | G | 41 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(38): Show |
41 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+11056delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | ||||||
chr4:74186438 | GAAAA | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+11053_451+1105 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | ||||||
chr4:74186457 | A | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+11054A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186457 | |||||||
chr4:74186615 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451+11212T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186615 | |||||||
chr4:74186632 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.451+11229A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186632 | |||||||
chr4:74186771 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+11368A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186771 | |||||||
chr4:74186875 | A | G | 99 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(96): Show |
99 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.451+11472A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186875 | |||||||
chr4:74186920 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.451+11517C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186920 | |||||||
chr4:74186961 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.451+11558T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186961 | |||||||
chr4:74187112 | C | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.451+11709C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187112 | |||||||
chr4:74187253 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0003g0138 |
2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.451+11850C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187253 | |||||||
chr4:74187288 | G | A | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+11885G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187288 | |||||||
chr4:74187312 | C | A | 1 | a0001c0001t0003g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.451+11909C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187312 | |||||||
chr4:74187432 | G | A | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+12029G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187432 | |||||||
chr4:74187707 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.452-12087G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187707 | |||||||
chr4:74187733 | T | TAC | 24 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0001g0068 others(21): Show |
24 | HG00280.hp1 HG01123.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-12024_452-1202 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187733 | T | TACAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(7): Show |
11 | HG01891.hp2 HG02083.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-12026_452-1202 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187733 | TAC | T | 15 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
15 | HG01243.hp1 HG01884.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.452-12024_452-1202 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187733 | TACAC | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(21): Show |
24 | HG01109.hp2 HG01123.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.452-12026_452-1202 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187733 | TACACAC | T | 43 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0048 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.452-12028_452-1202 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187733 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0065 a0001c0001t0002g0066 a0001c0001t0002g0155 |
3 | HG02965.hp1 HG03041.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.452-12030_452-1202 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | ||||||
chr4:74187786 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-12008T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187786 | |||||||
chr4:74187800 | T | TAC | 14 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0008 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-11960_452-1195 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACAC | 2 | a0001c0001t0002g0155 a0001c0001t0003g0060 |
2 | HG01496.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.452-11962_452-1195 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACAC | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-11964_452-1195 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01123.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-11966_452-1195 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(3): Show |
5 | a0001c0001t0001g0042 a0001c0001t0002g0177 a0001c0001t0003g0174 others(2): Show |
5 | HG01109.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-11968_452-1195 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(5): Show |
10 | a0001c0001t0001g0015 a0001c0001t0001g0193 a0001c0001t0002g0050 others(7): Show |
10 | HG02647.hp2 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-11970_452-1195 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0051 a0001c0001t0002g0154 a0001c0001t0003g0041 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-11972_452-1195 others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(9): Show |
6 | a0001c0001t0002g0137 a0001c0001t0002g0194 a0001c0001t0003g0059 others(3): Show |
6 | HG02129.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-11974_452-1195 others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(11): Show |
3 | a0001c0001t0001g0048 a0001c0001t0003g0039 a0001c0001t0003g0040 |
3 | NA18973.hp1 NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.452-11976_452-1195 others(22): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(13): Show |
5 | a0001c0001t0001g0049 a0001c0001t0002g0045 a0001c0001t0003g0038 others(2): Show |
5 | HG02040.hp2 HG03239.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-11978_452-1195 others(24): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(15): Show |
3 | a0001c0001t0003g0036 a0001c0001t0003g0046 a0001c0003t0004g0047 |
3 | HG02165.hp1 NA18522.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.452-11980_452-1195 others(26): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(17): Show |
4 | a0001c0001t0001g0044 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): Show |
4 | HG01106.hp2 HG02735.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-11982_452-1195 others(28): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(19): Show |
2 | a0001c0001t0001g0043 a0001c0001t0003g0037 |
2 | NA18994.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.452-11984_452-1195 others(30): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(21): Show |
1 | a0001c0001t0003g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.452-11986_452-1195 others(32): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | T | TACACACA others(23): Show |
1 | a0001c0001t0003g0027 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.452-11988_452-1195 others(34): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0002g0002 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-11968_452-1195 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187800 | TACACACA others(5): Show |
T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(106): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.452-11970_452-1195 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | ||||||
chr4:74187850 | C | G | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.452-11944C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187850 | |||||||
chr4:74187888 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.452-11906T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187888 | |||||||
chr4:74188122 | CTG | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.452-11669_452-1166 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188122 | ||||||
chr4:74188172 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.452-11622C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188172 | |||||||
chr4:74188419 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.452-11375T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188419 | |||||||
chr4:74188488 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0002g0066 |
2 | HG03041.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.452-11306C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188488 | |||||||
chr4:74188517 | T | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-11277T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188517 | |||||||
chr4:74188678 | GTA | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
60 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.452-11104_452-1110 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188678 | ||||||
chr4:74188680 | A | ATATATAT others(133): Show |
1 | a0001c0001t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.452-11105_452-1110 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188680 | ||||||
chr4:74188682 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.452-11103_452-1110 others(40): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188682 | ||||||
chr4:74188682 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-11105_452-1110 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188682 | ||||||
chr4:74188698 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0002g0045 |
3 | HG01071.hp1 NA18954.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.452-11096G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188698 | |||||||
chr4:74188698 | G | GCATATGT others(27): Show |
105 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(102): Show |
106 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.452-11069_452-1106 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188698 | ||||||
chr4:74188716 | GTATATAT others(33): Show |
G | 7 | a0001c0001t0001g0156 a0001c0001t0002g0002 a0001c0001t0002g0003 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-11068_452-1102 others(44): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188716 | ||||||
chr4:74188728 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.452-11066G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188728 | |||||||
chr4:74188735 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.452-11059C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188735 | |||||||
chr4:74188740 | GTA | G | 6 | a0001c0001t0001g0151 a0001c0001t0002g0045 a0001c0001t0002g0157 others(3): Show |
6 | HG02486.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-11044_452-1104 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188740 | ||||||
chr4:74188742 | A | ATATATAT others(135): Show |
4 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | NA18973.hp1 NA18991.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(146): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(27): Show |
18 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0002g0008 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(135): Show |
1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(146): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(133): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(169): Show |
1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(180): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(61): Show |
2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-11045_452-1104 others(72): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(133): Show |
38 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(169): Show |
7 | a0001c0001t0001g0144 a0001c0001t0002g0142 a0001c0001t0002g0143 others(4): Show |
7 | HG02258.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(180): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(131): Show |
2 | a0001c0001t0003g0171 a0001c0001t0003g0172 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.452-11045_452-1104 others(142): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATATAT others(167): Show |
1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(178): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188742 | A | ATATGGGT others(23): Show |
1 | a0001c0001t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.452-11049_452-1104 others(34): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | ||||||
chr4:74188750 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(99): Show |
103 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.452-11044A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188750 | |||||||
chr4:74188751 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(99): Show |
103 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.452-11043T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188751 | |||||||
chr4:74188753 | G | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(99): Show |
103 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.452-11041G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188753 | |||||||
chr4:74188754 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(99): Show |
103 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.452-11040G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188754 | |||||||
chr4:74188778 | GTA | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-11006_452-1100 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188778 | ||||||
chr4:74188792 | GTA | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
11 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-10992_452-1099 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188792 | ||||||
chr4:74188822 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.452-10972A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188822 | |||||||
chr4:74188875 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-10919C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188875 | |||||||
chr4:74189030 | C | T | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-10764C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189030 | |||||||
chr4:74189441 | G | A | 2 | a0001c0001t0003g0101 a0001c0005t0001g0099 |
2 | NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.452-10353G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189441 | |||||||
chr4:74189485 | C | CCTTTTT | 5 | a0001c0001t0001g0049 a0001c0001t0003g0046 a0001c0001t0003g0054 others(2): Show |
5 | HG02165.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT | 25 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
25 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT others(1): Show |
15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0042 others(12): Show |
15 | HG01109.hp2 HG01891.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT others(3): Show |
2 | a0001c0001t0002g0164 a0001c0001t0003g0026 |
2 | HG01243.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.452-10309_452-1030 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT others(4): Show |
9 | a0001c0001t0001g0144 a0001c0001t0002g0137 a0001c0001t0002g0142 others(6): Show |
9 | HG02258.hp2 HG03041.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT others(5): Show |
3 | a0001c0001t0001g0193 a0001c0001t0002g0145 a0001c0001t0002g0194 |
3 | HG03471.hp2 HG03704.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452-10309_452-1030 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | C | CCTTTTTT others(6): Show |
1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-10309_452-1030 others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | |||||||
chr4:74189485 | CT | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-10284delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | ||||||
chr4:74189485 | CTT | C | 12 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0124 others(9): Show |
12 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-10285_452-1028 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | ||||||
chr4:74189485 | CTTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(87): Show |
91 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.452-10286_452-1028 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | ||||||
chr4:74189485 | CTTTT | C | 15 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0085 others(12): Show |
15 | HG01070.hp1 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10287_452-1028 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | ||||||
chr4:74189485 | CTTTTT | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0018 others(5): Show |
8 | HG01071.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-10288_452-1028 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | ||||||
chr4:74189487 | T | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-10307T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189487 | |||||||
chr4:74189488 | T | C | 12 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0124 others(9): Show |
12 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-10306T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189488 | |||||||
chr4:74189489 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(87): Show |
91 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.452-10305T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189489 | |||||||
chr4:74189490 | T | C | 15 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0085 others(12): Show |
15 | HG01070.hp1 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10304T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189490 | |||||||
chr4:74189491 | T | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0018 others(5): Show |
8 | HG01071.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-10303T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189491 | |||||||
chr4:74189492 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.452-10302T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189492 | |||||||
chr4:74189691 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.452-10103A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189691 | |||||||
chr4:74189754 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.452-10040T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189754 | |||||||
chr4:74189816 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-9978T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189816 | |||||||
chr4:74190112 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.452-9682A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190112 | |||||||
chr4:74190174 | C | CT | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.452-9619dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74190174 | ||||||
chr4:74190275 | T | C | 64 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
64 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.452-9519T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190275 | |||||||
chr4:74190373 | G | A | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-9421G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190373 | |||||||
chr4:74190499 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0197 |
2 | HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.452-9295C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190499 | |||||||
chr4:74190614 | C | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-9180C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190614 | |||||||
chr4:74190932 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.452-8862G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190932 | |||||||
chr4:74191146 | C | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-8648C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191146 | |||||||
chr4:74191214 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-8580T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191214 | |||||||
chr4:74191283 | T | C | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.452-8511T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191283 | |||||||
chr4:74191363 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-8431C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191363 | |||||||
chr4:74191364 | G | GT | 39 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
39 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.452-8419dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74191364 | ||||||
chr4:74191379 | G | A | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-8415G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191379 | |||||||
chr4:74191388 | G | T | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-8406G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191388 | |||||||
chr4:74191540 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.452-8254T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191540 | |||||||
chr4:74191581 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.452-8213T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191581 | |||||||
chr4:74191660 | C | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0188 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-8134C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191660 | |||||||
chr4:74191718 | T | A | 2 | a0001c0001t0001g0156 a0001c0001t0003g0192 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.452-8076T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191718 | |||||||
chr4:74192035 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.452-7759A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192035 | |||||||
chr4:74192095 | T | G | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.452-7699T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192095 | |||||||
chr4:74192174 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.452-7620C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192174 | |||||||
chr4:74192249 | C | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-7545C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192249 | |||||||
chr4:74192254 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-7540C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192254 | |||||||
chr4:74192321 | T | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0048 others(17): Show |
20 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.452-7473T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192321 | |||||||
chr4:74192362 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.452-7432A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192362 | |||||||
chr4:74192521 | T | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-7273T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192521 | |||||||
chr4:74192633 | C | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(124): Show |
128 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.452-7161C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192633 | |||||||
chr4:74192719 | A | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
64 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.452-7075A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192719 | |||||||
chr4:74192790 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.452-7004A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192790 | |||||||
chr4:74193066 | T | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.452-6728T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193066 | |||||||
chr4:74193115 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-6679T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193115 | |||||||
chr4:74193223 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0110 a0001c0001t0003g0192 |
3 | HG01169.hp2 HG03579.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.452-6571C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193223 | |||||||
chr4:74193240 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.452-6554G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193240 | |||||||
chr4:74193314 | TTGTC | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.452-6476_452-6473d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74193314 | ||||||
chr4:74193370 | T | C | 1 | a0001c0001t0003g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.452-6424T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193370 | |||||||
chr4:74193597 | T | G | 4 | a0001c0001t0001g0013 a0001c0001t0002g0159 a0001c0001t0002g0163 others(1): Show |
4 | HG01243.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-6197T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193597 | |||||||
chr4:74193623 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.452-6171T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193623 | |||||||
chr4:74193776 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.452-6018T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193776 | |||||||
chr4:74193789 | T | G | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-6005T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193789 | |||||||
chr4:74193877 | C | A | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.452-5917C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193877 | |||||||
chr4:74193879 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.452-5915A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193879 | |||||||
chr4:74193935 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.452-5859G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193935 | |||||||
chr4:74193976 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.452-5818T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193976 | |||||||
chr4:74194385 | A | AT | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-5400dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194385 | ||||||
chr4:74194418 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0065 others(20): Show |
24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-5376A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194418 | |||||||
chr4:74194708 | G | C | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.452-5086G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194708 | |||||||
chr4:74194850 | C | CT | 39 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(36): Show |
39 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.452-4937dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194850 | ||||||
chr4:74194850 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(44): Show |
48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-4944C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194850 | |||||||
chr4:74194866 | ATCT | A | 6 | a0001c0001t0001g0078 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG00597.hp2 NA18945.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-4921_452-4919d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194866 | ||||||
chr4:74194881 | G | A | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(84): Show |
87 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.452-4913G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194881 | |||||||
chr4:74195382 | C | A | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-4412C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195382 | |||||||
chr4:74195423 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.452-4371G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195423 | |||||||
chr4:74195471 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0065 others(20): Show |
24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-4323T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195471 | |||||||
chr4:74195779 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.452-4015T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195779 | |||||||
chr4:74195843 | G | T | 1 | a0001c0001t0001g0033 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.452-3951G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195843 | |||||||
chr4:74195927 | G | A | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-3867G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195927 | |||||||
chr4:74196348 | T | G | 3 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-3446T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196348 | |||||||
chr4:74196501 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.452-3293T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196501 | |||||||
chr4:74196553 | A | T | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-3241A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196553 | |||||||
chr4:74196622 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(48): Show |
52 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.452-3172A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196622 | |||||||
chr4:74196727 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.452-3067C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196727 | |||||||
chr4:74196771 | C | T | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-3023C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196771 | |||||||
chr4:74196895 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.452-2899G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196895 | |||||||
chr4:74196945 | C | CA | 19 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0078 others(16): Show |
19 | HG00597.hp2 HG01070.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.452-2831dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74196945 | ||||||
chr4:74197384 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-2410C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197384 | |||||||
chr4:74197608 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.452-2186G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197608 | |||||||
chr4:74197659 | T | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0002g0008 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-2135T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197659 | |||||||
chr4:74197689 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.452-2105C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197689 | |||||||
chr4:74198013 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(44): Show |
48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-1781T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198013 | |||||||
chr4:74198024 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.452-1770G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198024 | |||||||
chr4:74198290 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.452-1504C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198290 | |||||||
chr4:74198506 | CT | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(44): Show |
48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-1284delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74198506 | ||||||
chr4:74198552 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.452-1242T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198552 | |||||||
chr4:74198606 | T | A | 2 | a0001c0001t0001g0081 a0001c0003t0004g0047 |
2 | HG01261.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-1188T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198606 | |||||||
chr4:74198607 | A | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-1187A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198607 | |||||||
chr4:74198884 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.452-910G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198884 | |||||||
chr4:74199351 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-443C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199351 | |||||||
chr4:74199387 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-407A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199387 | |||||||
chr4:74199487 | C | G | 1 | a0001c0001t0003g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-307C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199487 | |||||||
chr4:74199645 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-149G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199645 | |||||||
chr4:74199647 | A | AAAT | 22 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(19): Show |
22 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.452-125_452-123dup others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74199647 | ||||||
chr4:74199647 | A | AAATAAT | 3 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-128_452-123dup others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74199647 | ||||||
chr4:74199761 | T | A | 1 | a0001c0003t0004g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.452-33T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199761 | |||||||
chr4:74200341 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.604+395A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200341 | |||||||
chr4:74200369 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.604+423C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200369 | |||||||
chr4:74200698 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0007g0055 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.605-565G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200698 | |||||||
chr4:74200847 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.605-416A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200847 | |||||||
chr4:74200869 | CTT | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0065 others(20): Show |
24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-391_605-390del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 74200869 | ||||||
chr4:74200894 | G | A | 14 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0074 others(11): Show |
14 | HG01109.hp2 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.605-369G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200894 | |||||||
chr4:74201129 | CATATT | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.605-130_605-126del others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 74201129 | ||||||
chr4:74201148 | A | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-115A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74201148 | |||||||
chr4:74201257 | T | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0002g0008 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.605-6T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74201257 | |||||||
chr4:74201399 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+29C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201399 | |||||||
chr4:74201421 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.712+51T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201421 | |||||||
chr4:74201452 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.712+82A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201452 | |||||||
chr4:74201502 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712+132A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201502 | |||||||
chr4:74201568 | AT | A | 142 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(139): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.712+212delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | ||||||
chr4:74201568 | ATT | A | 43 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.712+211_712+212del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | ||||||
chr4:74201568 | ATTT | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+210_712+212del others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | ||||||
chr4:74201616 | T | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0005g0141 others(1): Show |
4 | HG02895.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+246T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201616 | |||||||
chr4:74201710 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(135): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.712+340G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201710 | |||||||
chr4:74202021 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.712+651C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202021 | |||||||
chr4:74202036 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.712+666G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202036 | |||||||
chr4:74202082 | C | T | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+712C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202082 | |||||||
chr4:74202094 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.712+724C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202094 | |||||||
chr4:74202125 | C | T | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(84): Show |
87 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.712+755C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202125 | |||||||
chr4:74202157 | T | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0005g0141 others(1): Show |
4 | HG02895.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+787T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202157 | |||||||
chr4:74202224 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712+854G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202224 | |||||||
chr4:74202225 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712+855G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202225 | |||||||
chr4:74202537 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0065 others(20): Show |
24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+1167T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202537 | |||||||
chr4:74202715 | C | T | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+1345C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202715 | |||||||
chr4:74202870 | G | A | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+1500G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202870 | |||||||
chr4:74202942 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.712+1572C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202942 | |||||||
chr4:74203200 | T | TAAAAAGC others(327): Show |
4 | a0001c0001t0001g0193 a0001c0001t0002g0045 a0001c0001t0002g0194 others(1): Show |
4 | HG03704.hp2 NA18954.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+1847_712+1848i others(336): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203200 | ||||||
chr4:74203200 | T | TAAAAAGC others(328): Show |
3 | a0001c0001t0002g0137 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG03831.hp1 HG03927.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.712+1847_712+1848i others(337): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203200 | ||||||
chr4:74203331 | T | TTC | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+1973_712+1974d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203331 | ||||||
chr4:74203372 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+2002C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203372 | |||||||
chr4:74203411 | G | T | 8 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0002g0008 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+2041G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203411 | |||||||
chr4:74203474 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.712+2104G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203474 | |||||||
chr4:74203897 | GT | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.712+2540delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203897 | ||||||
chr4:74204039 | C | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+2669C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204039 | |||||||
chr4:74204194 | C | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0193 a0001c0001t0002g0045 others(8): Show |
11 | HG02486.hp1 HG02970.hp2 HG03579.hp1 others(8): Show |
intron_variant | MODIFIER | c.712+2824C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204194 | |||||||
chr4:74204247 | CAAT | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0065 others(20): Show |
24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+2882_712+2884d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74204247 | ||||||
chr4:74204822 | T | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0002g0008 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+3452T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204822 | |||||||
chr4:74204960 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0123 |
3 | HG03927.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.712+3590C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204960 | |||||||
chr4:74205040 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.712+3670C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205040 | |||||||
chr4:74205258 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.712+3888C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205258 | |||||||
chr4:74205314 | G | A | 19 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(16): Show |
19 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.712+3944G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205314 | |||||||
chr4:74205448 | G | A | 10 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0019 others(7): Show |
10 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.712+4078G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205448 | |||||||
chr4:74205473 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0152 |
2 | HG02040.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.712+4103T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205473 | |||||||
chr4:74205588 | T | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+4218T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205588 | |||||||
chr4:74205696 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+4326G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205696 | |||||||
chr4:74205852 | A | AT | 24 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0079 others(21): Show |
24 | HG00438.hp2 HG00621.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+4483dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74205852 | ||||||
chr4:74205884 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.712+4514A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205884 | |||||||
chr4:74206010 | A | G | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG00438.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.712+4640A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206010 | |||||||
chr4:74206134 | T | TA | 30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
30 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.712+4778dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206134 | ||||||
chr4:74206187 | AT | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0088 |
2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.712+4820delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206187 | ||||||
chr4:74206322 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(12): Show |
16 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.712+4952G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206322 | |||||||
chr4:74206383 | C | CTGGAATT others(1): Show |
25 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0002g0050 others(22): Show |
25 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.712+5016_712+5023d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206383 | ||||||
chr4:74206389 | T | G | 1 | a0002c0002t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.712+5019T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206389 | |||||||
chr4:74206399 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+5029G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206399 | |||||||
chr4:74206843 | TACTA | T | 2 | a0001c0001t0003g0185 a0001c0003t0004g0047 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.712+5477_712+5480d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206843 | ||||||
chr4:74207092 | G | T | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(60): Show |
63 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.712+5722G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207092 | |||||||
chr4:74207159 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.712+5789C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207159 | |||||||
chr4:74207165 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0156 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.712+5795G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207165 | |||||||
chr4:74207198 | C | T | 154 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.712+5828C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207198 | |||||||
chr4:74207313 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.712+5943T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207313 | |||||||
chr4:74207585 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.712+6215C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207585 | |||||||
chr4:74207589 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.712+6219G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207589 | |||||||
chr4:74207683 | C | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+6313C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207683 | |||||||
chr4:74207759 | A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+6389A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207759 | |||||||
chr4:74207760 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+6390A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207760 | |||||||
chr4:74207766 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0052 a0001c0001t0003g0171 a0001c0001t0003g0172 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+6403_712+6412d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(4): Show |
59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0015 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.712+6402_712+6412d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0189 others(5): Show |
8 | HG01123.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+6401_712+6412d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.712+6400_712+6412d others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0155 a0001c0001t0003g0167 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.712+6399_712+6412d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+6398_712+6412d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207766 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0020 others(1): Show |
4 | HG01243.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+6397_712+6412d others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | ||||||
chr4:74207776 | T | TTTTTTTT others(8): Show |
1 | a0001c0001t0002g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.712+6412_712+6413i others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207776 | ||||||
chr4:74207915 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.712+6545T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207915 | |||||||
chr4:74207983 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+6613A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207983 | |||||||
chr4:74208082 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.712+6712A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208082 | |||||||
chr4:74208303 | A | ATTCAGTG others(10): Show |
168 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(165): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.712+6935_712+6951d others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74208303 | ||||||
chr4:74208303 | A | ATTTCAGT others(11): Show |
1 | a0001c0001t0001g0112 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.712+6935_712+6936i others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74208303 | ||||||
chr4:74208414 | C | G | 169 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(166): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.712+7044C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208414 | |||||||
chr4:74208470 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.712+7100C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208470 | |||||||
chr4:74208671 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.712+7301G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208671 | |||||||
chr4:74208707 | C | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.712+7337C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208707 | |||||||
chr4:74208832 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.712+7462A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208832 | |||||||
chr4:74208854 | A | G | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0108 others(3): Show |
6 | HG02004.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.712+7484A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208854 | |||||||
chr4:74209136 | C | T | 86 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0042 others(83): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.712+7766C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209136 | |||||||
chr4:74209285 | T | C | 68 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.712+7915T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209285 | |||||||
chr4:74209586 | G | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+8216G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209586 | |||||||
chr4:74209768 | A | G | 8 | a0001c0001t0002g0045 a0001c0001t0002g0131 a0001c0001t0002g0137 others(5): Show |
8 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+8398A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209768 | |||||||
chr4:74209952 | A | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+8582A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209952 | |||||||
chr4:74210176 | C | CA | 169 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(166): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.712+8806_712+8807i others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210176 | |||||||
chr4:74210288 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.712+8918G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210288 | |||||||
chr4:74210561 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+9191C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210561 | |||||||
chr4:74210655 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+9285G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210655 | |||||||
chr4:74210672 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+9302C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210672 | |||||||
chr4:74210992 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(12): Show |
16 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.712+9622T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210992 | |||||||
chr4:74211082 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+9712G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211082 | |||||||
chr4:74211135 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.712+9765C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211135 | |||||||
chr4:74211299 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.712+9929A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211299 | |||||||
chr4:74211308 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.712+9938T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211308 | |||||||
chr4:74211340 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+9970T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211340 | |||||||
chr4:74211349 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+9979A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211349 | |||||||
chr4:74212294 | G | A | 5 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0004g0016 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+10924G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212294 | |||||||
chr4:74212402 | C | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0195 others(1): Show |
4 | HG03927.hp1 NA19004.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+11032C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212402 | |||||||
chr4:74212443 | C | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.712+11073C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212443 | |||||||
chr4:74212546 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(22): Show |
26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11176G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212546 | |||||||
chr4:74212712 | G | A | 60 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.712+11342G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212712 | |||||||
chr4:74212801 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+11431T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212801 | |||||||
chr4:74212900 | A | T | 25 | a0001c0001t0001g0048 a0001c0001t0003g0027 a0001c0001t0003g0028 others(22): Show |
25 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.712+11530A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212900 | |||||||
chr4:74213106 | G | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(22): Show |
26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11736G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213106 | |||||||
chr4:74213119 | C | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(22): Show |
26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11749C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213119 | |||||||
chr4:74213349 | C | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-11953C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213349 | |||||||
chr4:74213781 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0002c0002t0001g0076 |
3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.713-11521G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213781 | |||||||
chr4:74214059 | A | C | 3 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0004t0001g0012 |
3 | HG02572.hp2 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-11243A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214059 | |||||||
chr4:74214165 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
109 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.713-11137T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214165 | |||||||
chr4:74214186 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.713-11116C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214186 | |||||||
chr4:74214311 | G | C | 8 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(5): Show |
8 | HG01106.hp2 HG02015.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-10991G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214311 | |||||||
chr4:74214341 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(22): Show |
26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.713-10961G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214341 | |||||||
chr4:74214403 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.713-10899G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214403 | |||||||
chr4:74214730 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(22): Show |
26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.713-10572G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214730 | |||||||
chr4:74214874 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-10428G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214874 | |||||||
chr4:74214923 | T | C | 4 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0053 others(1): Show |
4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.713-10379T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214923 | |||||||
chr4:74214924 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.713-10378G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214924 | |||||||
chr4:74215076 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
109 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.713-10226C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215076 | |||||||
chr4:74215325 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-9977G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215325 | |||||||
chr4:74215362 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-9940G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215362 | |||||||
chr4:74215399 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-9903G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215399 | |||||||
chr4:74215404 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-9898G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215404 | |||||||
chr4:74215467 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.713-9835G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215467 | |||||||
chr4:74215968 | GA | G | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.713-9323delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74215968 | ||||||
chr4:74216067 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713-9235G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216067 | |||||||
chr4:74216395 | T | C | 169 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(166): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.713-8907T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216395 | |||||||
chr4:74216488 | C | T | 86 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0042 others(83): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.713-8814C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216488 | |||||||
chr4:74216785 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.713-8517A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216785 | |||||||
chr4:74216834 | C | A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0042 others(83): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.713-8468C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216834 | |||||||
chr4:74217010 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-8292C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217010 | |||||||
chr4:74217112 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.713-8190C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217112 | |||||||
chr4:74217285 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.713-8017A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217285 | |||||||
chr4:74217344 | A | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.713-7958A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217344 | |||||||
chr4:74217384 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.713-7918A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217384 | |||||||
chr4:74217619 | C | T | 86 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0042 others(83): Show |
86 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.713-7683C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217619 | |||||||
chr4:74217872 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7430A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217872 | |||||||
chr4:74217899 | T | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7403T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217899 | |||||||
chr4:74218027 | G | A | 3 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0004t0001g0012 |
3 | HG02572.hp2 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-7275G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218027 | |||||||
chr4:74218050 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7252T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218050 | |||||||
chr4:74218250 | A | T | 88 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0042 others(85): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.713-7052A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218250 | |||||||
chr4:74218296 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.713-7006A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218296 | |||||||
chr4:74218519 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0183 |
3 | HG02630.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.713-6783T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218519 | |||||||
chr4:74218614 | G | GC | 31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0122 others(28): Show |
32 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.713-6678dupC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74218614 | ||||||
chr4:74218614 | GC | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0082 others(28): Show |
31 | HG01099.hp1 HG01109.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.713-6678delC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74218614 | ||||||
chr4:74218661 | T | C | 44 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(41): Show |
44 | HG00408.hp1 HG01099.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.713-6641T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218661 | |||||||
chr4:74218839 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.713-6463C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218839 | |||||||
chr4:74218992 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | HG02132.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.713-6310T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218992 | |||||||
chr4:74219087 | G | A | 161 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(158): Show |
161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.713-6215G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219087 | |||||||
chr4:74219185 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(14): Show |
18 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.713-6117G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219185 | |||||||
chr4:74219464 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.713-5838C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219464 | |||||||
chr4:74219525 | G | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-5777G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219525 | |||||||
chr4:74219820 | A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-5482A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219820 | |||||||
chr4:74219841 | C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-5461C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219841 | |||||||
chr4:74219927 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.713-5375C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219927 | |||||||
chr4:74219929 | C | T | 161 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(158): Show |
161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.713-5373C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219929 | |||||||
chr4:74220092 | A | AT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
164 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.713-5199dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74220092 | ||||||
chr4:74220467 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.713-4835T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220467 | |||||||
chr4:74220509 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.713-4793T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220509 | |||||||
chr4:74220704 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.713-4598G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220704 | |||||||
chr4:74220754 | C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-4548C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220754 | |||||||
chr4:74220875 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.713-4427A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220875 | |||||||
chr4:74221132 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0182 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.713-4170G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221132 | |||||||
chr4:74221208 | TATTA | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-4088_713-4085d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74221208 | ||||||
chr4:74221382 | A | G | 1 | a0001c0001t0003g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.713-3920A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221382 | |||||||
chr4:74221455 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-3847T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221455 | |||||||
chr4:74221874 | T | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-3428T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221874 | |||||||
chr4:74221921 | T | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-3381T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221921 | |||||||
chr4:74221942 | T | C | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.713-3360T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221942 | |||||||
chr4:74222119 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.713-3183A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222119 | |||||||
chr4:74222128 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.713-3174A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222128 | |||||||
chr4:74222180 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.713-3122C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222180 | |||||||
chr4:74222338 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.713-2964C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222338 | |||||||
chr4:74222665 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-2637G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222665 | |||||||
chr4:74222911 | A | G | 1 | a0001c0001t0003g0101 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.713-2391A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222911 | |||||||
chr4:74223125 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG02965.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.713-2177T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223125 | |||||||
chr4:74223262 | T | A | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.713-2040T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223262 | |||||||
chr4:74223404 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.713-1898G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223404 | |||||||
chr4:74223638 | A | AAAAT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.713-1654_713-1651d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74223638 | ||||||
chr4:74224025 | T | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-1277T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224025 | |||||||
chr4:74224057 | G | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
18 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.713-1245G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224057 | |||||||
chr4:74224159 | C | A | 2 | a0001c0001t0003g0036 a0001c0001t0003g0040 |
2 | NA18973.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.713-1143C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224159 | |||||||
chr4:74224187 | C | T | 10 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0181 others(7): Show |
10 | HG02572.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-1115C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224187 | |||||||
chr4:74224315 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0002g0018 |
2 | HG02622.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.713-987C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224315 | |||||||
chr4:74224511 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.713-791G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224511 | |||||||
chr4:74224531 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.713-771G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224531 | |||||||
chr4:74224800 | A | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.713-502A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224800 | |||||||
chr4:74224906 | CA | C | 6 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0002g0184 others(3): Show |
6 | HG02572.hp1 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.713-394delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74224906 | ||||||
chr4:74225055 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-247T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74225055 | |||||||
chr4:74225120 | G | C | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.713-182G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74225120 | |||||||
chr4:74225521 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+127A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225521 | |||||||
chr4:74225870 | A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+476A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225870 | |||||||
chr4:74225881 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+487T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225881 | |||||||
chr4:74226190 | CA | C | 46 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0063 others(43): Show |
46 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.805+806delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74226190 | ||||||
chr4:74226213 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+819A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74226213 | |||||||
chr4:74227743 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+2349A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227743 | |||||||
chr4:74227825 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+2431A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227825 | |||||||
chr4:74227922 | A | T | 10 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0026 others(7): Show |
10 | HG00280.hp1 HG00621.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.805+2528A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227922 | |||||||
chr4:74227923 | A | T | 10 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0026 others(7): Show |
10 | HG00280.hp1 HG00621.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.805+2529A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227923 | |||||||
chr4:74227991 | C | T | 72 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
72 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.805+2597C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227991 | |||||||
chr4:74227992 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0156 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805+2598A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227992 | |||||||
chr4:74227995 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+2601T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227995 | |||||||
chr4:74228474 | T | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+3080T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228474 | |||||||
chr4:74228737 | G | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+3343G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228737 | |||||||
chr4:74228874 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3480G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228874 | |||||||
chr4:74228938 | G | A | 1 | a0001c0001t0003g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.805+3544G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228938 | |||||||
chr4:74229119 | C | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3725C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229119 | |||||||
chr4:74229245 | A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3851A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229245 | |||||||
chr4:74229344 | C | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+3950C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229344 | |||||||
chr4:74229463 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.805+4069A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229463 | |||||||
chr4:74229504 | G | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+4110G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229504 | |||||||
chr4:74229528 | A | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+4134A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229528 | |||||||
chr4:74229688 | G | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+4294G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229688 | |||||||
chr4:74230029 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.805+4635G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230029 | |||||||
chr4:74230244 | C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+4850C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230244 | |||||||
chr4:74230318 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
82 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.805+4924A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230318 | |||||||
chr4:74230591 | GA | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
164 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.805+5211delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74230591 | ||||||
chr4:74230602 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+5208A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230602 | |||||||
chr4:74230684 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+5290C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230684 | |||||||
chr4:74230735 | G | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.805+5341G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230735 | |||||||
chr4:74230767 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.805+5373C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230767 | |||||||
chr4:74230823 | A | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+5429A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230823 | |||||||
chr4:74231002 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.805+5608C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231002 | |||||||
chr4:74231058 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+5664T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231058 | |||||||
chr4:74231297 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+5903G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231297 | |||||||
chr4:74231483 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+6089A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231483 | |||||||
chr4:74231771 | A | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+6377A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231771 | |||||||
chr4:74232404 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.805+7010C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232404 | |||||||
chr4:74232774 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.805+7380T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232774 | |||||||
chr4:74232869 | G | GAT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0108 others(3): Show |
6 | HG02004.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+7479_805+7480d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74232869 | ||||||
chr4:74232951 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.805+7557G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232951 | |||||||
chr4:74232952 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.805+7558C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232952 | |||||||
chr4:74232992 | C | T | 77 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+7598C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232992 | |||||||
chr4:74233005 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+7611G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233005 | |||||||
chr4:74233037 | ATTAC | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.805+7647_805+7650d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74233037 | ||||||
chr4:74233083 | A | G | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.805+7689A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233083 | |||||||
chr4:74233398 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+8004T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233398 | |||||||
chr4:74233951 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.805+8557T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233951 | |||||||
chr4:74234203 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0088 |
2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.805+8809T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234203 | |||||||
chr4:74234497 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+9103T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234497 | |||||||
chr4:74234796 | A | AATGT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+9402_805+9403i others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234796 | |||||||
chr4:74234796 | A | AGT | 8 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0107 others(5): Show |
8 | HG01123.hp2 HG01496.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.805+9425_805+9426d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | A | AGTGT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(8): Show |
12 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.805+9423_805+9426d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | A | AGTGTGT | 19 | a0001c0001t0001g0065 a0001c0001t0001g0193 a0001c0001t0002g0002 others(16): Show |
19 | HG01106.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.805+9421_805+9426d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | A | AGTGTGTG others(1): Show |
54 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(51): Show |
54 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.805+9419_805+9426d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0002g0056 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.805+9417_805+9426d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+9415_805+9426d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | AGT | A | 26 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0018 others(23): Show |
26 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.805+9425_805+9426d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234796 | AGTGT | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0159 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.805+9423_805+9426d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | ||||||
chr4:74234810 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.805+9416T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234810 | |||||||
chr4:74234824 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(75): Show |
78 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.805+9430C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234824 | |||||||
chr4:74234978 | A | G | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+9584A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234978 | |||||||
chr4:74235000 | A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+9606A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235000 | |||||||
chr4:74235420 | T | C | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0158 others(8): Show |
11 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+10026T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235420 | |||||||
chr4:74235582 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+10188T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235582 | |||||||
chr4:74235586 | G | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0092 |
2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.805+10192G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235586 | |||||||
chr4:74235678 | G | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+10284G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235678 | |||||||
chr4:74235784 | G | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+10390G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235784 | |||||||
chr4:74235851 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+10457C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235851 | |||||||
chr4:74236142 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+10748T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236142 | |||||||
chr4:74236154 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.805+10760C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236154 | |||||||
chr4:74236282 | T | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+10888T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236282 | |||||||
chr4:74236372 | T | G | 1 | a0001c0001t0003g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+10978T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236372 | |||||||
chr4:74236538 | T | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+11144T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236538 | |||||||
chr4:74236705 | G | A | 1 | a0001c0001t0002g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+11311G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236705 | |||||||
chr4:74236905 | T | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+11511T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236905 | |||||||
chr4:74236931 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+11537A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236931 | |||||||
chr4:74236972 | G | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+11578G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236972 | |||||||
chr4:74237028 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(73): Show |
77 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+11634A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237028 | |||||||
chr4:74237065 | C | T | 13 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0018 others(10): Show |
13 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.805+11671C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237065 | |||||||
chr4:74237170 | G | A | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+11776G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237170 | |||||||
chr4:74237186 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+11792A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237186 | |||||||
chr4:74237276 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.805+11882T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237276 | |||||||
chr4:74237569 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+12175G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237569 | |||||||
chr4:74237571 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+12177A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237571 | |||||||
chr4:74237585 | G | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
18 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+12191G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237585 | |||||||
chr4:74237693 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.805+12299G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237693 | |||||||
chr4:74237952 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+12558C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237952 | |||||||
chr4:74237959 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(70): Show |
74 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+12565C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237959 | |||||||
chr4:74237981 | G | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(73): Show |
77 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+12587G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237981 | |||||||
chr4:74238049 | T | C | 4 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0053 others(1): Show |
4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+12655T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238049 | |||||||
chr4:74238272 | G | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+12878G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238272 | |||||||
chr4:74238276 | G | A | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805+12882G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238276 | |||||||
chr4:74238289 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+12895T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238289 | |||||||
chr4:74238300 | G | C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0145 a0001c0001t0002g0165 |
3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.805+12906G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238300 | |||||||
chr4:74238604 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+13210C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238604 | |||||||
chr4:74238679 | A | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+13285A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238679 | |||||||
chr4:74238800 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.805+13406G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238800 | |||||||
chr4:74238971 | G | C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0145 a0001c0001t0002g0165 |
3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.805+13577G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238971 | |||||||
chr4:74239110 | A | C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+13716A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239110 | |||||||
chr4:74239222 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
79 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.805+13828A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239222 | |||||||
chr4:74239294 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+13900T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239294 | |||||||
chr4:74239429 | T | C | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+14035T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239429 | |||||||
chr4:74239489 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805+14095T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239489 | |||||||
chr4:74239489 | T | TA | 85 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+14095_805+1409 others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239489 | |||||||
chr4:74239490 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+14096T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239490 | |||||||
chr4:74239491 | A | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.805+14097A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239491 | |||||||
chr4:74239706 | C | A | 3 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.805+14312C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239706 | |||||||
chr4:74239731 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0129 others(1): Show |
4 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+14337T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239731 | |||||||
chr4:74239885 | C | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+14491C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239885 | |||||||
chr4:74240203 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+14809G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240203 | |||||||
chr4:74240397 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.805+15003G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240397 | |||||||
chr4:74240474 | G | C | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+15080G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240474 | |||||||
chr4:74240648 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+15254C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240648 | |||||||
chr4:74240712 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.805+15318T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240712 | |||||||
chr4:74240768 | A | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG00438.hp1 HG00621.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.805+15374A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240768 | |||||||
chr4:74240774 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.805+15380A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240774 | |||||||
chr4:74241006 | TG | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+15614delG | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74241006 | ||||||
chr4:74241110 | G | A | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+15716G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241110 | |||||||
chr4:74241151 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805+15757A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241151 | |||||||
chr4:74241153 | A | G | 66 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(63): Show |
66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+15759A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241153 | |||||||
chr4:74241161 | A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+15767A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241161 | |||||||
chr4:74241418 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+16024G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241418 | |||||||
chr4:74241538 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
82 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.805+16144T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241538 | |||||||
chr4:74241540 | C | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+16146C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241540 | |||||||
chr4:74241608 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+16214A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241608 | |||||||
chr4:74241673 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.805+16279C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241673 | |||||||
chr4:74241680 | A | G | 66 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(63): Show |
66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+16286A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241680 | |||||||
chr4:74241708 | C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+16314C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241708 | |||||||
chr4:74241807 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+16413T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241807 | |||||||
chr4:74241843 | C | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+16449C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241843 | |||||||
chr4:74241948 | C | T | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+16554C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241948 | |||||||
chr4:74242080 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.805+16686G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242080 | |||||||
chr4:74242200 | A | AAAAAT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+16811_805+1681 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74242200 | ||||||
chr4:74242234 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.805+16840A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242234 | |||||||
chr4:74242235 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0109 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.805+16841G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242235 | |||||||
chr4:74242603 | C | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+17209C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242603 | |||||||
chr4:74242670 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.805+17276G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242670 | |||||||
chr4:74242769 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+17375A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242769 | |||||||
chr4:74242797 | T | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+17403T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242797 | |||||||
chr4:74242854 | A | G | 45 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(42): Show |
45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.805+17460A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242854 | |||||||
chr4:74242873 | C | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+17479C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242873 | |||||||
chr4:74243291 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.805+17897C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243291 | |||||||
chr4:74243343 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0002g0142 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.805+17949C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243343 | |||||||
chr4:74243423 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(3): Show |
7 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+18029C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243423 | |||||||
chr4:74243770 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+18376C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243770 | |||||||
chr4:74243862 | A | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.805+18468A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243862 | |||||||
chr4:74243994 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.805+18600A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243994 | |||||||
chr4:74244040 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+18646G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244040 | |||||||
chr4:74244050 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+18656C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244050 | |||||||
chr4:74244078 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+18684A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244078 | |||||||
chr4:74244215 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+18821A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244215 | |||||||
chr4:74244291 | T | C | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+18897T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244291 | |||||||
chr4:74244389 | T | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0053 others(1): Show |
4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+18995T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244389 | |||||||
chr4:74244412 | G | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.805+19018G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244412 | |||||||
chr4:74244470 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+19076A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244470 | |||||||
chr4:74244512 | TTA | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
82 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.805+19122_805+1912 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74244512 | ||||||
chr4:74244796 | A | G | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+19402A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244796 | |||||||
chr4:74244803 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.805+19409A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244803 | |||||||
chr4:74244823 | T | G | 81 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.805+19429T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244823 | |||||||
chr4:74244916 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+19522C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244916 | |||||||
chr4:74245051 | G | A | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.805+19657G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245051 | |||||||
chr4:74245068 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+19674G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245068 | |||||||
chr4:74245097 | A | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+19703A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245097 | |||||||
chr4:74245119 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.805+19725C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245119 | |||||||
chr4:74245120 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0120 |
3 | HG00438.hp1 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.805+19726G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245120 | |||||||
chr4:74245194 | C | CA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0122 others(3): Show |
6 | HG00408.hp1 HG01243.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+19825dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245194 | ||||||
chr4:74245194 | CA | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(127): Show |
131 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.805+19825delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245194 | ||||||
chr4:74245298 | T | A | 5 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(2): Show |
5 | HG02015.hp2 NA18973.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+19904T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245298 | |||||||
chr4:74245385 | T | C | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805+19991T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245385 | |||||||
chr4:74245481 | AT | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20095delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245481 | ||||||
chr4:74245601 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+20207A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245601 | |||||||
chr4:74245662 | G | A | 45 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(42): Show |
45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.805+20268G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245662 | |||||||
chr4:74245723 | T | C | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20329T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245723 | |||||||
chr4:74245738 | T | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0129 others(1): Show |
4 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+20344T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245738 | |||||||
chr4:74245839 | G | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0182 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.805+20445G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245839 | |||||||
chr4:74245950 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.805+20556A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245950 | |||||||
chr4:74246027 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+20633G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246027 | |||||||
chr4:74246054 | G | C | 76 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+20660G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246054 | |||||||
chr4:74246063 | A | G | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20669A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246063 | |||||||
chr4:74246101 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.805+20707A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246101 | |||||||
chr4:74246210 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20816G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246210 | |||||||
chr4:74246229 | T | A | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.805+20835T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246229 | |||||||
chr4:74246249 | T | C | 13 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(10): Show |
13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.805+20855T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246249 | |||||||
chr4:74246286 | G | T | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+20892G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246286 | |||||||
chr4:74246354 | G | A | 66 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(63): Show |
66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+20960G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246354 | |||||||
chr4:74246622 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.805+21228T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246622 | |||||||
chr4:74246727 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+21333A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246727 | |||||||
chr4:74246770 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+21376T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246770 | |||||||
chr4:74246785 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805+21391G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246785 | |||||||
chr4:74246786 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805+21392A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246786 | |||||||
chr4:74246796 | C | T | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+21402C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246796 | |||||||
chr4:74246797 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.805+21403G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246797 | |||||||
chr4:74246807 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.805+21413C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246807 | |||||||
chr4:74246829 | T | C | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.805+21435T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246829 | |||||||
chr4:74246951 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.805+21557T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246951 | |||||||
chr4:74246954 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+21560C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246954 | |||||||
chr4:74246959 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+21565C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246959 | |||||||
chr4:74246989 | C | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.805+21595C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246989 | |||||||
chr4:74247087 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.805+21693A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247087 | |||||||
chr4:74247149 | T | C | 3 | a0001c0001t0003g0011 a0001c0001t0003g0052 a0001c0001t0003g0167 |
3 | HG02145.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.805+21755T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247149 | |||||||
chr4:74247254 | G | A | 1 | a0001c0003t0004g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805+21860G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247254 | |||||||
chr4:74247351 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.805+21957T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247351 | |||||||
chr4:74247365 | G | T | 41 | a0001c0001t0001g0051 a0001c0001t0003g0011 a0001c0001t0003g0025 others(38): Show |
41 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.805+21971G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247365 | |||||||
chr4:74247388 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+21994A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247388 | |||||||
chr4:74247490 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+22096G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247490 | |||||||
chr4:74247556 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.805+22162C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247556 | |||||||
chr4:74247582 | G | T | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.805+22188G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247582 | |||||||
chr4:74247630 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.805+22236G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247630 | |||||||
chr4:74247640 | T | A | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+22246T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247640 | |||||||
chr4:74247695 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
92 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.805+22301G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247695 | |||||||
chr4:74247742 | T | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0066 a0001c0001t0002g0143 others(6): Show |
9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.805+22348T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247742 | |||||||
chr4:74247798 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+22404A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247798 | |||||||
chr4:74247810 | T | C | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.805+22416T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247810 | |||||||
chr4:74247876 | G | T | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+22482G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247876 | |||||||
chr4:74247948 | G | T | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+22554G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247948 | |||||||
chr4:74247994 | T | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+22600T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247994 | |||||||
chr4:74248099 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.805+22705C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248099 | |||||||
chr4:74248166 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.805+22772C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248166 | |||||||
chr4:74248256 | G | C | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.805+22862G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248256 | |||||||
chr4:74248349 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+22955C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248349 | |||||||
chr4:74248350 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.805+22956G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248350 | |||||||
chr4:74248365 | C | T | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+22971C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248365 | |||||||
chr4:74248473 | T | C | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+23079T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248473 | |||||||
chr4:74248559 | T | G | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.805+23165T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248559 | |||||||
chr4:74248846 | C | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.805+23452C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248846 | |||||||
chr4:74248967 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.805+23573G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248967 | |||||||
chr4:74249157 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+23763G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249157 | |||||||
chr4:74249294 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.805+23900G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249294 | |||||||
chr4:74249347 | C | T | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.805+23953C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249347 | |||||||
chr4:74249431 | A | T | 1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+24037A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249431 | |||||||
chr4:74249436 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.805+24042A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249436 | |||||||
chr4:74249576 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.805+24182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249576 | |||||||
chr4:74249606 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.805+24212C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249606 | |||||||
chr4:74249674 | T | C | 8 | a0001c0001t0002g0019 a0001c0001t0002g0143 a0001c0001t0002g0145 others(5): Show |
8 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+24280T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249674 | |||||||
chr4:74249732 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.805+24338A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249732 | |||||||
chr4:74249815 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+24421C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249815 | |||||||
chr4:74249838 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.805+24444G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249838 | |||||||
chr4:74249839 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.805+24445C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249839 | |||||||
chr4:74249896 | T | C | 77 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+24502T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249896 | |||||||
chr4:74249942 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805+24548A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249942 | |||||||
chr4:74249963 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+24569G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249963 | |||||||
chr4:74250021 | T | TG | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.805+24628dupG | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74250021 | ||||||
chr4:74250042 | A | G | 77 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(74): Show |
77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+24648A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250042 | |||||||
chr4:74250141 | C | G | 1 | a0001c0001t0003g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.805+24747C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250141 | |||||||
chr4:74250198 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.805+24804A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250198 | |||||||
chr4:74250242 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+24848T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250242 | |||||||
chr4:74250280 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.805+24886A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250280 | |||||||
chr4:74250296 | T | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+24902T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250296 | |||||||
chr4:74250633 | C | T | 11 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0066 others(8): Show |
11 | HG01243.hp2 HG02622.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+25239C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250633 | |||||||
chr4:74250750 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.805+25356T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250750 | |||||||
chr4:74251020 | A | G | 9 | a0001c0001t0002g0019 a0001c0001t0002g0066 a0001c0001t0002g0143 others(6): Show |
9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.805+25626A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251020 | |||||||
chr4:74251146 | A | G | 41 | a0001c0001t0001g0051 a0001c0001t0003g0011 a0001c0001t0003g0025 others(38): Show |
41 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.805+25752A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251146 | |||||||
chr4:74251377 | A | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+25983A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251377 | |||||||
chr4:74251392 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805+25998A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251392 | |||||||
chr4:74251643 | C | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.805+26249C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251643 | |||||||
chr4:74251716 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.805+26322A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251716 | |||||||
chr4:74251737 | A | G | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+26343A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251737 | |||||||
chr4:74252023 | T | C | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+26629T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252023 | |||||||
chr4:74252086 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.805+26692C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252086 | |||||||
chr4:74252362 | A | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+26968A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252362 | |||||||
chr4:74252493 | A | T | 1 | a0001c0001t0003g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.805+27099A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252493 | |||||||
chr4:74252537 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+27143C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252537 | |||||||
chr4:74252537 | CAAG | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | HG00438.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.805+27146_805+2714 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74252537 | ||||||
chr4:74252646 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.805+27252C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252646 | |||||||
chr4:74252694 | T | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+27300T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252694 | |||||||
chr4:74253022 | G | T | 76 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(73): Show |
76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+27628G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253022 | |||||||
chr4:74253251 | A | G | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+27857A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253251 | |||||||
chr4:74253284 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.805+27890C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253284 | |||||||
chr4:74253351 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.805+27957T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253351 | |||||||
chr4:74253356 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+27962G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253356 | |||||||
chr4:74254114 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-27311G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254114 | |||||||
chr4:74254239 | T | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0184 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.806-27186T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254239 | |||||||
chr4:74254330 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.806-27095C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254330 | |||||||
chr4:74254510 | T | C | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.806-26915T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254510 | |||||||
chr4:74254570 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26855A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254570 | |||||||
chr4:74254571 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26854A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254571 | |||||||
chr4:74254587 | C | CA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.806-26825dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254587 | ||||||
chr4:74254587 | C | CAA | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.806-26826_806-2682 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254587 | ||||||
chr4:74254636 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26789A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254636 | |||||||
chr4:74254645 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.806-26780C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254645 | |||||||
chr4:74254714 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.806-26711G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254714 | |||||||
chr4:74254757 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26668A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254757 | |||||||
chr4:74254762 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26663G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254762 | |||||||
chr4:74254767 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-26658G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254767 | |||||||
chr4:74254781 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26644A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254781 | |||||||
chr4:74254807 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.806-26618C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254807 | |||||||
chr4:74254830 | T | TTA | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.806-26594_806-2659 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254830 | ||||||
chr4:74254836 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.806-26589G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254836 | |||||||
chr4:74254909 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806-26516C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254909 | |||||||
chr4:74254990 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-26435C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254990 | |||||||
chr4:74255028 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.806-26397G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255028 | |||||||
chr4:74255136 | C | CA | 26 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
26 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.806-26264dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | ||||||
chr4:74255136 | C | CAA | 48 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0043 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.806-26265_806-2626 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | ||||||
chr4:74255136 | C | CAAA | 12 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0051 others(9): Show |
12 | HG00621.hp1 HG01109.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-26266_806-2626 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | ||||||
chr4:74255136 | CA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
81 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.806-26264delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | ||||||
chr4:74255140 | A | C | 8 | a0001c0001t0002g0158 a0001c0001t0002g0177 a0001c0001t0002g0181 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-26285A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255140 | |||||||
chr4:74255351 | A | G | 6 | a0001c0001t0003g0083 a0001c0001t0003g0086 a0001c0001t0003g0087 others(3): Show |
6 | HG02083.hp2 NA18939.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.806-26074A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255351 | |||||||
chr4:74255436 | AGAAAG | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0167 |
2 | HG02145.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.806-25985_806-2598 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255436 | ||||||
chr4:74255491 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.806-25934T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255491 | |||||||
chr4:74255540 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.806-25885C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255540 | |||||||
chr4:74255631 | C | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0128 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.806-25794C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255631 | |||||||
chr4:74255641 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.806-25784C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255641 | |||||||
chr4:74255688 | T | A | 2 | a0001c0001t0002g0155 a0001c0004t0001g0012 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.806-25737T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255688 | |||||||
chr4:74256003 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.806-25422A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256003 | |||||||
chr4:74256255 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806-25170G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256255 | |||||||
chr4:74256656 | C | G | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.806-24769C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256656 | |||||||
chr4:74256780 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.806-24645G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256780 | |||||||
chr4:74256825 | T | C | 9 | a0001c0001t0002g0019 a0001c0001t0002g0066 a0001c0001t0002g0143 others(6): Show |
9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-24600T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256825 | |||||||
chr4:74256915 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.806-24510T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256915 | |||||||
chr4:74257184 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.806-24241T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257184 | |||||||
chr4:74257335 | C | T | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-24090C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257335 | |||||||
chr4:74257337 | G | A | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-24088G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257337 | |||||||
chr4:74257381 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.806-24044G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257381 | |||||||
chr4:74257418 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-24007A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257418 | |||||||
chr4:74257942 | T | C | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-23483T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257942 | |||||||
chr4:74257987 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.806-23438C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257987 | |||||||
chr4:74258318 | G | C | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.806-23107G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258318 | |||||||
chr4:74258389 | A | AAC | 11 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-23016_806-2301 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74258389 | ||||||
chr4:74258643 | T | A | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-22782T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258643 | |||||||
chr4:74258787 | C | T | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-22638C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258787 | |||||||
chr4:74259093 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.806-22332A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259093 | |||||||
chr4:74259123 | A | C | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-22302A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259123 | |||||||
chr4:74259148 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-22277C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259148 | |||||||
chr4:74259293 | G | C | 49 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.806-22132G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259293 | |||||||
chr4:74259558 | T | C | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-21867T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259558 | |||||||
chr4:74259932 | A | G | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.806-21493A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259932 | |||||||
chr4:74260302 | C | T | 3 | a0001c0001t0002g0143 a0001c0001t0002g0145 a0001c0001t0002g0165 |
3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.806-21123C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260302 | |||||||
chr4:74260373 | A | G | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-21052A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260373 | |||||||
chr4:74260709 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-20716C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260709 | |||||||
chr4:74260756 | C | G | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.806-20669C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260756 | |||||||
chr4:74260856 | C | T | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-20569C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260856 | |||||||
chr4:74260923 | CAAAG | C | 99 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.806-20498_806-2049 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74260923 | ||||||
chr4:74261011 | G | GAA | 15 | a0001c0001t0001g0069 a0001c0001t0002g0008 a0001c0001t0002g0009 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.806-20408_806-2040 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261011 | ||||||
chr4:74261011 | GA | G | 11 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-20407delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261011 | ||||||
chr4:74261017 | A | AAT | 3 | a0001c0001t0001g0118 a0001c0001t0002g0137 a0001c0001t0007g0055 |
3 | HG02109.hp2 HG02647.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.806-20394_806-2039 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261017 | ||||||
chr4:74261018 | AT | A | 69 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
69 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.806-20406delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261018 | |||||||
chr4:74261019 | T | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0109 a0001c0001t0002g0010 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-20406T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261019 | |||||||
chr4:74261375 | TCA | T | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-20047_806-2004 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261375 | ||||||
chr4:74261727 | A | G | 2 | a0001c0001t0002g0181 a0001c0001t0002g0184 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.806-19698A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261727 | |||||||
chr4:74261745 | A | G | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-19680A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261745 | |||||||
chr4:74262055 | A | ATATAT | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-19368_806-1936 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74262055 | ||||||
chr4:74262077 | C | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-19348C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262077 | |||||||
chr4:74262188 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-19237G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262188 | |||||||
chr4:74262200 | A | C | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-19225A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262200 | |||||||
chr4:74262248 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.806-19177T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262248 | |||||||
chr4:74262310 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.806-19115C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262310 | |||||||
chr4:74262319 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.806-19106A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262319 | |||||||
chr4:74262362 | A | C | 3 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.806-19063A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262362 | |||||||
chr4:74262514 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
2 | NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.806-18911G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262514 | |||||||
chr4:74262759 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.806-18666A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262759 | |||||||
chr4:74262771 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0146 |
2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.806-18654T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262771 | |||||||
chr4:74262789 | T | C | 3 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.806-18636T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262789 | |||||||
chr4:74262959 | A | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-18466A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262959 | |||||||
chr4:74263200 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.806-18225G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263200 | |||||||
chr4:74263784 | T | G | 29 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-17641T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263784 | |||||||
chr4:74263823 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.806-17602C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263823 | |||||||
chr4:74264017 | A | T | 11 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0002g0155 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-17408A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264017 | |||||||
chr4:74264523 | T | G | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-16902T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264523 | |||||||
chr4:74264744 | G | A | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-16681G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264744 | |||||||
chr4:74264768 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-16657T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264768 | |||||||
chr4:74264779 | C | A | 2 | a0001c0001t0003g0036 a0001c0001t0003g0040 |
2 | NA18973.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.806-16646C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264779 | |||||||
chr4:74265112 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.806-16313A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265112 | |||||||
chr4:74265243 | T | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-16182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265243 | |||||||
chr4:74265726 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
150 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.806-15699C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265726 | |||||||
chr4:74266182 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.806-15243G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266182 | |||||||
chr4:74266228 | TA | T | 17 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0045 others(14): Show |
17 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.806-15196delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266228 | |||||||
chr4:74266569 | G | A | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-14856G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266569 | |||||||
chr4:74266614 | A | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-14811A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266614 | |||||||
chr4:74266636 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0146 |
3 | HG01978.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.806-14789C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266636 | |||||||
chr4:74266931 | T | C | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-14494T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266931 | |||||||
chr4:74266979 | T | G | 1 | a0001c0001t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.806-14446T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266979 | |||||||
chr4:74267081 | C | T | 118 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(115): Show |
118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.806-14344C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267081 | |||||||
chr4:74267243 | A | G | 1 | a0001c0005t0001g0099 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.806-14182A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267243 | |||||||
chr4:74267304 | CT | C | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-14117delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267304 | ||||||
chr4:74267319 | CT | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0143 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.806-14103delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267319 | ||||||
chr4:74267327 | CT | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0143 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.806-14095delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267327 | ||||||
chr4:74267371 | T | TTTTC | 10 | a0001c0001t0001g0093 a0001c0001t0002g0155 a0001c0001t0002g0158 others(7): Show |
10 | HG02135.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-14034_806-1403 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267371 | ||||||
chr4:74267371 | T | TTTTCTTT others(9): Show |
1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-14046_806-1403 others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267371 | ||||||
chr4:74267372 | T | TTTCTTTC others(28): Show |
1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-14031_806-1403 others(39): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267372 | ||||||
chr4:74267434 | A | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-13991A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267434 | |||||||
chr4:74267615 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-13810T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267615 | |||||||
chr4:74267700 | T | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-13725T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267700 | |||||||
chr4:74267882 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-13543C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267882 | |||||||
chr4:74267969 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-13456C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267969 | |||||||
chr4:74267996 | G | A | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-13429G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267996 | |||||||
chr4:74268021 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.806-13404G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268021 | |||||||
chr4:74268189 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-13236T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268189 | |||||||
chr4:74268470 | A | G | 2 | a0001c0001t0003g0185 a0001c0003t0004g0047 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.806-12955A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268470 | |||||||
chr4:74268906 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.806-12519A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268906 | |||||||
chr4:74269171 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.806-12254T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269171 | |||||||
chr4:74269288 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-12137A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269288 | |||||||
chr4:74269379 | A | G | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-12046A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269379 | |||||||
chr4:74269425 | A | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0139 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-12000A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269425 | |||||||
chr4:74269460 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-11965T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269460 | |||||||
chr4:74270101 | T | A | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-11324T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270101 | |||||||
chr4:74270177 | A | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-11248A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270177 | |||||||
chr4:74270355 | G | C | 1 | a0001c0001t0002g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.806-11070G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270355 | |||||||
chr4:74270521 | T | C | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-10904T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270521 | |||||||
chr4:74270583 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806-10842G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270583 | |||||||
chr4:74270612 | G | A | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10813G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270612 | |||||||
chr4:74270650 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806-10775T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270650 | |||||||
chr4:74270655 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.806-10770G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270655 | |||||||
chr4:74270711 | G | A | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10714G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270711 | |||||||
chr4:74270794 | C | A | 110 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
110 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.806-10631C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270794 | |||||||
chr4:74270919 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-10506C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270919 | |||||||
chr4:74270925 | G | T | 110 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
110 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.806-10500G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270925 | |||||||
chr4:74270986 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0120 |
3 | HG00438.hp1 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.806-10439T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270986 | |||||||
chr4:74271043 | C | T | 108 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(105): Show |
108 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.806-10382C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271043 | |||||||
chr4:74271297 | G | A | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
17 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.806-10128G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271297 | |||||||
chr4:74271304 | G | T | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10121G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271304 | |||||||
chr4:74271371 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.806-10054T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271371 | |||||||
chr4:74271442 | T | G | 11 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0002g0155 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-9983T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271442 | |||||||
chr4:74271454 | C | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-9971C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271454 | |||||||
chr4:74271523 | G | C | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-9902G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271523 | |||||||
chr4:74271537 | T | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-9888T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271537 | |||||||
chr4:74271587 | T | A | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-9838T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271587 | |||||||
chr4:74271610 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.806-9815C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271610 | |||||||
chr4:74271643 | G | C | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-9782G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271643 | |||||||
chr4:74271651 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.806-9774G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271651 | |||||||
chr4:74271680 | A | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-9745A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271680 | |||||||
chr4:74271874 | GA | G | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
17 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.806-9550delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271874 | |||||||
chr4:74271898 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.806-9527T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271898 | |||||||
chr4:74272010 | T | C | 9 | a0001c0001t0002g0155 a0001c0001t0002g0158 a0001c0001t0002g0177 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-9415T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272010 | |||||||
chr4:74272023 | A | C | 11 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0002g0155 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-9402A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272023 | |||||||
chr4:74272050 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.806-9375G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272050 | |||||||
chr4:74272307 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0014 |
2 | HG01123.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.806-9118C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272307 | |||||||
chr4:74272581 | G | A | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-8844G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272581 | |||||||
chr4:74272662 | A | T | 11 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0002g0155 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-8763A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272662 | |||||||
chr4:74272805 | C | T | 45 | a0001c0001t0001g0051 a0001c0001t0003g0011 a0001c0001t0003g0025 others(42): Show |
45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.806-8620C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272805 | |||||||
chr4:74272949 | A | T | 11 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0002g0155 others(8): Show |
11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-8476A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272949 | |||||||
chr4:74273143 | A | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-8282A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273143 | |||||||
chr4:74273524 | C | T | 114 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-7901C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273524 | |||||||
chr4:74273613 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0003g0057 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.806-7812A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273613 | |||||||
chr4:74273938 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-7487C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273938 | |||||||
chr4:74274012 | A | AT | 86 | a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0003 others(83): Show |
86 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.806-7403dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74274012 | ||||||
chr4:74274290 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-7135G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274290 | |||||||
chr4:74274596 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-6829A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274596 | |||||||
chr4:74274602 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.806-6823C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274602 | |||||||
chr4:74274734 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-6691C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274734 | |||||||
chr4:74274814 | A | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0100 |
3 | NA18965.hp2 NA18968.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.806-6611A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274814 | |||||||
chr4:74275039 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.806-6386C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275039 | |||||||
chr4:74275406 | T | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(54): Show |
57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-6019T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275406 | |||||||
chr4:74275570 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-5855A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275570 | |||||||
chr4:74275640 | C | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.806-5785C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275640 | |||||||
chr4:74275934 | A | C | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-5491A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275934 | |||||||
chr4:74275969 | T | A | 115 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.806-5456T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275969 | |||||||
chr4:74276008 | G | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(42): Show |
45 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.806-5417G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276008 | |||||||
chr4:74276361 | A | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-5064A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276361 | |||||||
chr4:74276571 | C | A | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.806-4854C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276571 | |||||||
chr4:74276596 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-4829G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276596 | |||||||
chr4:74276631 | A | T | 10 | a0001c0001t0002g0019 a0001c0001t0002g0066 a0001c0001t0002g0142 others(7): Show |
10 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-4794A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276631 | |||||||
chr4:74276729 | C | T | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-4696C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276729 | |||||||
chr4:74276892 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.806-4533A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276892 | |||||||
chr4:74277135 | C | T | 13 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(10): Show |
13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.806-4290C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277135 | |||||||
chr4:74277154 | A | AT | 40 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0003 others(37): Show |
40 | HG00280.hp1 HG00621.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.806-4256dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | ||||||
chr4:74277154 | A | ATT | 23 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0034 others(20): Show |
23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.806-4257_806-4256d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | ||||||
chr4:74277154 | AT | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
54 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.806-4256delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | ||||||
chr4:74277305 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-4120A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277305 | |||||||
chr4:74277355 | C | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-4070C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277355 | |||||||
chr4:74277356 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(54): Show |
57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-4069G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277356 | |||||||
chr4:74277365 | G | A | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0176 |
3 | HG01109.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.806-4060G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277365 | |||||||
chr4:74277418 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806-4007G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277418 | |||||||
chr4:74277485 | A | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-3940A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277485 | |||||||
chr4:74277726 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.806-3699C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277726 | |||||||
chr4:74277805 | A | ATTTG | 30 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(27): Show |
30 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.806-3592_806-3589d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277805 | ||||||
chr4:74277805 | A | ATTTGTTT others(1): Show |
3 | a0001c0001t0002g0020 a0001c0001t0002g0105 a0001c0001t0007g0055 |
3 | HG01891.hp1 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.806-3596_806-3589d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277805 | ||||||
chr4:74278023 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-3402C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278023 | |||||||
chr4:74278026 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-3399G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278026 | |||||||
chr4:74278157 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.806-3268G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278157 | |||||||
chr4:74278171 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.806-3254A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278171 | |||||||
chr4:74278291 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-3134A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278291 | |||||||
chr4:74278377 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.806-3048T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278377 | |||||||
chr4:74278449 | A | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-2976A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278449 | |||||||
chr4:74278856 | T | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-2569T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278856 | |||||||
chr4:74278896 | A | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(54): Show |
57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-2529A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278896 | |||||||
chr4:74279005 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.806-2420C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279005 | |||||||
chr4:74279079 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.806-2346C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279079 | |||||||
chr4:74279199 | A | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0052 a0001c0001t0003g0167 |
3 | HG02145.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.806-2226A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279199 | |||||||
chr4:74279480 | T | G | 2 | a0001c0001t0003g0148 a0001c0001t0003g0153 |
2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.806-1945T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279480 | |||||||
chr4:74279697 | A | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(54): Show |
57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-1728A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279697 | |||||||
chr4:74279749 | A | G | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-1676A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279749 | |||||||
chr4:74279818 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-1607A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279818 | |||||||
chr4:74279864 | T | C | 115 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.806-1561T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279864 | |||||||
chr4:74279922 | A | G | 1 | a0001c0005t0001g0099 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.806-1503A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279922 | |||||||
chr4:74280047 | A | G | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.806-1378A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280047 | |||||||
chr4:74280078 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-1347G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280078 | |||||||
chr4:74280215 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-1210G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280215 | |||||||
chr4:74280426 | A | G | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-999A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280426 | |||||||
chr4:74280607 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.806-818A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280607 | |||||||
chr4:74280630 | GT | G | 101 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(98): Show |
101 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.806-783delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280630 | ||||||
chr4:74280630 | GTT | G | 8 | a0001c0001t0002g0050 a0001c0001t0002g0158 a0001c0001t0002g0177 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-784_806-783del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280630 | ||||||
chr4:74280642 | T | A | 39 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0108 others(36): Show |
39 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.806-783T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280642 | |||||||
chr4:74280642 | T | TA | 4 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0129 others(1): Show |
4 | HG01978.hp2 HG01981.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-777dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280642 | ||||||
chr4:74280642 | TA | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.806-777delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280642 | ||||||
chr4:74280643 | A | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-782A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280643 | |||||||
chr4:74280840 | TAAAA | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-583_806-580del others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280840 | ||||||
chr4:74281078 | A | T | 1 | a0001c0001t0002g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.806-347A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281078 | |||||||
chr4:74281108 | G | A | 43 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.806-317G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281108 | |||||||
chr4:74281196 | G | T | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-229G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281196 | |||||||
chr4:74281271 | C | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0002c0002t0001g0076 |
3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.806-154C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281271 | |||||||
chr4:74281324 | C | CGT | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG02083.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.806-76_806-75dupGT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0022 a0001c0001t0002g0019 a0001c0001t0002g0050 others(5): Show |
8 | HG02970.hp2 HG03195.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-84_806-75dupGT others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0002g0010 a0001c0001t0002g0142 a0001c0001t0002g0145 others(6): Show |
9 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-86_806-75dupGT others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(7): Show |
70 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0030 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.806-88_806-75dupGT others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(9): Show |
15 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0189 others(12): Show |
15 | HG00621.hp1 HG01109.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.806-90_806-75dupGT others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(11): Show |
12 | a0001c0001t0001g0032 a0001c0001t0002g0002 a0001c0001t0002g0003 others(9): Show |
12 | HG00408.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.806-92_806-75dupGT others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281324 | C | CGTGTGTG others(13): Show |
4 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-94_806-75dupGT others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | ||||||
chr4:74281341 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.806-84G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281341 | |||||||
chr4:74282108 | A | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+558A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282108 | |||||||
chr4:74282171 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.931+621C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282171 | |||||||
chr4:74282278 | C | G | 23 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0034 others(20): Show |
23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+728C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282278 | |||||||
chr4:74282286 | G | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+736G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282286 | |||||||
chr4:74282404 | G | GTTCTTCT others(12): Show |
12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+855_931+856ins others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74282404 | ||||||
chr4:74282408 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+858C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282408 | |||||||
chr4:74282653 | T | C | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1103T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282653 | |||||||
chr4:74282792 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(53): Show |
56 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.931+1242T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282792 | |||||||
chr4:74282933 | A | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.931+1383A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282933 | |||||||
chr4:74282960 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+1410T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282960 | |||||||
chr4:74283004 | G | GC | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1455dupC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74283004 | ||||||
chr4:74283205 | A | G | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1655A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283205 | |||||||
chr4:74283237 | T | A | 30 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(27): Show |
30 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.931+1687T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283237 | |||||||
chr4:74283374 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.931+1824C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283374 | |||||||
chr4:74283438 | C | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(2): Show |
5 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+1888C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283438 | |||||||
chr4:74283649 | G | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2099G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283649 | |||||||
chr4:74283719 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.931+2169G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283719 | |||||||
chr4:74284035 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.931+2485A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284035 | |||||||
chr4:74284094 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2544G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284094 | |||||||
chr4:74284363 | T | C | 21 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(18): Show |
21 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.931+2813T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284363 | |||||||
chr4:74284419 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.931+2869T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284419 | |||||||
chr4:74284443 | T | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+2893T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284443 | |||||||
chr4:74284493 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.931+2943C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284493 | |||||||
chr4:74284584 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.931+3034G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284584 | |||||||
chr4:74284783 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.931+3233G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284783 | |||||||
chr4:74284930 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+3380G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284930 | |||||||
chr4:74285024 | C | G | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+3474C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285024 | |||||||
chr4:74285106 | T | C | 46 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(43): Show |
46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.931+3556T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285106 | |||||||
chr4:74285465 | A | G | 44 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0026 others(41): Show |
44 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+3915A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285465 | |||||||
chr4:74285708 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.931+4158C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285708 | |||||||
chr4:74285829 | G | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0193 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.931+4279G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285829 | |||||||
chr4:74285867 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+4317C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285867 | |||||||
chr4:74285961 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.931+4411A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285961 | |||||||
chr4:74286103 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.931+4553A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286103 | |||||||
chr4:74286192 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.931+4642C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286192 | |||||||
chr4:74286262 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.931+4712T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286262 | |||||||
chr4:74286719 | G | A | 21 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0026 others(18): Show |
21 | HG00280.hp1 HG00621.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+5169G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286719 | |||||||
chr4:74286853 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+5303T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286853 | |||||||
chr4:74287013 | A | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+5463A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287013 | |||||||
chr4:74287020 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18945.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.931+5470T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287020 | |||||||
chr4:74287140 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.931+5590A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287140 | |||||||
chr4:74287194 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+5644G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287194 | |||||||
chr4:74287293 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.931+5743A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287293 | |||||||
chr4:74287616 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.931+6066G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287616 | |||||||
chr4:74287701 | C | T | 23 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0034 others(20): Show |
23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+6151C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287701 | |||||||
chr4:74287964 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0105 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.931+6414G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287964 | |||||||
chr4:74287993 | A | G | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(53): Show |
56 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.931+6443A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287993 | |||||||
chr4:74288049 | T | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+6499T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288049 | |||||||
chr4:74288181 | G | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0094 |
3 | HG00438.hp2 NA19081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.931+6631G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288181 | |||||||
chr4:74288206 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+6656G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288206 | |||||||
chr4:74288240 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.931+6690G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288240 | |||||||
chr4:74288304 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+6754A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288304 | |||||||
chr4:74288364 | G | T | 1 | a0001c0001t0002g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.931+6814G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288364 | |||||||
chr4:74288479 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.931+6929T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288479 | |||||||
chr4:74288721 | G | A | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+7171G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288721 | |||||||
chr4:74288802 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.931+7252C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288802 | |||||||
chr4:74289179 | C | A | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+7629C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289179 | |||||||
chr4:74289509 | C | G | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+7959C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289509 | |||||||
chr4:74289717 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0014 |
2 | HG01123.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.931+8167G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289717 | |||||||
chr4:74289946 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+8396T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289946 | |||||||
chr4:74290019 | C | A | 32 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(29): Show |
32 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.931+8469C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290019 | |||||||
chr4:74290303 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.931+8753G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290303 | |||||||
chr4:74290322 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0105 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.931+8772A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290322 | |||||||
chr4:74290640 | C | CTGTG | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.931+9108_931+9111d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74290640 | ||||||
chr4:74291003 | C | CTTT | 11 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0090 others(8): Show |
11 | HG00597.hp2 HG00621.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+9483_931+9485d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0114 others(4): Show |
7 | HG02004.hp1 HG02040.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9482_931+9485d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01981.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9478_931+9485d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(8): Show |
11 | HG02004.hp2 HG02015.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+9477_931+9485d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00408.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.931+9476_931+9485d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.931+9475_931+9485d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.931+9473_931+9485d others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0043 |
2 | HG02965.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.931+9472_931+9485d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.931+9471_931+9485d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0015 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.931+9470_931+9485d others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0180 |
3 | HG01123.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.931+9469_931+9485d others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0144 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9468_931+9485d others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.931+9467_931+9485d others(21): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0073 others(6): Show |
9 | HG01123.hp2 HG01981.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.931+9466_931+9485d others(22): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0063 a0001c0001t0001g0080 a0001c0001t0001g0094 others(6): Show |
9 | HG01106.hp1 HG01978.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.931+9465_931+9485d others(23): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0091 others(2): Show |
5 | HG00408.hp2 HG01261.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9464_931+9485d others(24): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.931+9463_931+9485d others(25): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.931+9462_931+9485d others(26): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.931+9461_931+9485d others(27): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.931+9459_931+9485d others(29): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.931+9458_931+9485d others(30): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.931+9453C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291003 | |||||||
chr4:74291003 | CTTT | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0178 a0001c0001t0003g0036 others(5): Show |
8 | HG00597.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.931+9483_931+9485d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTT | C | 37 | a0001c0001t0001g0071 a0001c0001t0001g0149 a0001c0001t0002g0005 others(34): Show |
37 | HG00280.hp2 HG00621.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.931+9482_931+9485d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTTT | C | 14 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(11): Show |
14 | HG00280.hp1 HG01243.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+9481_931+9485d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTTTTT others(2): Show |
C | 29 | a0001c0001t0001g0067 a0001c0001t0002g0008 a0001c0001t0002g0009 others(26): Show |
29 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.931+9477_931+9485d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0160 |
2 | NA18954.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.931+9476_931+9485d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.931+9472_931+9485d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291003 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.931+9471_931+9485d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | ||||||
chr4:74291034 | TTGAGATG others(64): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.931+9485_931+9555d others(73): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291034 | |||||||
chr4:74291163 | G | A | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0176 |
3 | HG01109.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.931+9613G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291163 | |||||||
chr4:74291315 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+9765C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291315 | |||||||
chr4:74291372 | T | G | 89 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(86): Show |
89 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.931+9822T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291372 | |||||||
chr4:74291587 | T | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+10037T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291587 | |||||||
chr4:74291785 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0002g0018 |
2 | HG02622.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.932-9912A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291785 | |||||||
chr4:74292281 | T | C | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.932-9416T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292281 | |||||||
chr4:74292304 | A | T | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0004g0016 others(2): Show |
5 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-9393A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292304 | |||||||
chr4:74292313 | AT | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0002c0002t0001g0076 |
3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.932-9382delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74292313 | ||||||
chr4:74292515 | A | G | 88 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(85): Show |
88 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.932-9182A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292515 | |||||||
chr4:74292623 | A | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.932-9074A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292623 | |||||||
chr4:74292803 | G | A | 118 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(115): Show |
118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-8894G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292803 | |||||||
chr4:74293137 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.932-8560C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293137 | |||||||
chr4:74293188 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-8509C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293188 | |||||||
chr4:74293336 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.932-8361T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293336 | |||||||
chr4:74293348 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.932-8349A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293348 | |||||||
chr4:74293425 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.932-8272G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293425 | |||||||
chr4:74293502 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-8195T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293502 | |||||||
chr4:74293591 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.932-8106G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293591 | |||||||
chr4:74293755 | A | G | 1 | a0001c0001t0003g0036 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.932-7942A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293755 | |||||||
chr4:74294078 | C | G | 2 | a0001c0001t0003g0148 a0001c0001t0003g0153 |
2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.932-7619C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294078 | |||||||
chr4:74294338 | A | AT | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-7357dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74294338 | ||||||
chr4:74294486 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7211G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294486 | |||||||
chr4:74294494 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7203A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294494 | |||||||
chr4:74294500 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-7197A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294500 | |||||||
chr4:74294506 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.932-7191A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294506 | |||||||
chr4:74294859 | A | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-6838A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294859 | |||||||
chr4:74294936 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.932-6761G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294936 | |||||||
chr4:74295107 | C | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(43): Show |
46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-6590C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295107 | |||||||
chr4:74295177 | A | G | 46 | a0001c0001t0003g0011 a0001c0001t0003g0025 a0001c0001t0003g0026 others(43): Show |
46 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.932-6520A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295177 | |||||||
chr4:74295599 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.932-6098A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295599 | |||||||
chr4:74295670 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-6027T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295670 | |||||||
chr4:74295712 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.932-5985T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295712 | |||||||
chr4:74295935 | C | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(41): Show |
44 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.932-5762C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295935 | |||||||
chr4:74296083 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-5614C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296083 | |||||||
chr4:74296189 | C | T | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.932-5508C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296189 | |||||||
chr4:74296207 | T | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-5490T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296207 | |||||||
chr4:74296241 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-5456A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296241 | |||||||
chr4:74296480 | C | T | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-5217C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296480 | |||||||
chr4:74296481 | T | C | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-5216T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296481 | |||||||
chr4:74296581 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.932-5116C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296581 | |||||||
chr4:74296591 | A | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.932-5106A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296591 | |||||||
chr4:74296605 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.932-5092C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296605 | |||||||
chr4:74296753 | C | G | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-4944C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296753 | |||||||
chr4:74296754 | A | C | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-4943A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296754 | |||||||
chr4:74296961 | G | A | 118 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(115): Show |
118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-4736G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296961 | |||||||
chr4:74297030 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.932-4667T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297030 | |||||||
chr4:74297398 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-4299G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297398 | |||||||
chr4:74297425 | A | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(43): Show |
46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-4272A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297425 | |||||||
chr4:74297642 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-4055G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297642 | |||||||
chr4:74297703 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.932-3994C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297703 | |||||||
chr4:74297771 | CTT | C | 2 | a0001c0001t0003g0148 a0001c0001t0003g0153 |
2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.932-3924_932-3923d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74297771 | ||||||
chr4:74297780 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0017 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.932-3917A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297780 | |||||||
chr4:74297787 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.932-3910A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297787 | |||||||
chr4:74298312 | G | A | 14 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(11): Show |
14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.932-3385G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298312 | |||||||
chr4:74298450 | T | G | 1 | a0001c0001t0005g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.932-3247T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298450 | |||||||
chr4:74298487 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.932-3210C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298487 | |||||||
chr4:74298559 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.932-3138A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298559 | |||||||
chr4:74298566 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0091 |
2 | HG02109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.932-3131G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298566 | |||||||
chr4:74298851 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.932-2846T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298851 | |||||||
chr4:74298862 | T | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-2835T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298862 | |||||||
chr4:74299026 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.932-2671A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299026 | |||||||
chr4:74299088 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.932-2609A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299088 | |||||||
chr4:74299401 | CAGCAGT | C | 4 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0003g0026 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-2267_932-2262d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74299401 | ||||||
chr4:74299404 | CAGT | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-2290_932-2288d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74299404 | ||||||
chr4:74299413 | T | C | 31 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-2284T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299413 | |||||||
chr4:74299706 | C | G | 13 | a0001c0001t0002g0045 a0001c0001t0002g0115 a0001c0001t0002g0131 others(10): Show |
13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.932-1991C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299706 | |||||||
chr4:74299755 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.932-1942A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299755 | |||||||
chr4:74299780 | C | A | 2 | a0001c0001t0005g0141 a0001c0001t0005g0166 |
2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.932-1917C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299780 | |||||||
chr4:74299817 | C | T | 3 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0003t0004g0047 |
3 | HG02615.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-1880C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299817 | |||||||
chr4:74300033 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.932-1664G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300033 | |||||||
chr4:74300211 | T | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0009 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-1486T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300211 | |||||||
chr4:74300363 | A | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0056 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-1334A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300363 | |||||||
chr4:74300463 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.932-1234T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300463 | |||||||
chr4:74300853 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.932-844A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300853 | |||||||
chr4:74300870 | A | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-827A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300870 | |||||||
chr4:74301182 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0105 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.932-515G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301182 | |||||||
chr4:74301262 | A | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.932-435A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301262 | |||||||
chr4:74301354 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-343C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301354 | |||||||
chr4:74301355 | A | C | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.932-342A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301355 | |||||||
chr4:74301447 | G | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.932-250G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301447 | |||||||
chr4:74301464 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.932-233G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301464 | |||||||
chr4:74301530 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.932-167A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301530 | |||||||
chr4:74301532 | C | CGT | 23 | a0001c0001t0002g0010 a0001c0001t0002g0056 a0001c0001t0003g0027 others(20): Show |
23 | HG01099.hp2 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.932-140_932-139dup others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | ||||||
chr4:74301532 | CGT | C | 25 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(22): Show |
25 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.932-140_932-139del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | ||||||
chr4:74301532 | CGTGT | C | 9 | a0001c0001t0002g0019 a0001c0001t0002g0066 a0001c0001t0002g0142 others(6): Show |
9 | HG01243.hp2 HG02976.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.932-142_932-139del others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | ||||||
chr4:74301549 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.932-148G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301549 | |||||||
chr4:74301563 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.932-134T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301563 |