Item | Value |
---|---|
geneid | 6622 |
ensemblid | ENSG00000145335.17 |
hgncid | 11138 |
symbol | SNCA |
name | synuclein alpha |
refseq_nuc | NM_000345.4 |
refseq_prot | NP_000336.1 |
ensembl_nuc | ENST00000394991.8 |
ensembl_prot | ENSP00000378442.4 |
mane_status | MANE Select |
chr | chr4 |
start | 89724099 |
end | 89837161 |
strand | - |
ver | v1.2 |
region | chr4:89724099-89837161 |
region5000 | chr4:89719099-89842161 |
regionname0 | SNCA_chr4_89724099_89837161 |
regionname5000 | SNCA_chr4_89719099_89842161 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 140 | 337 | 82 | 64 | 148 | 10 | 33 | 116 | SNCA_chr4_89719099_89842161 | SNCA | MDVFM others(135): Show |
chr4 | 89719099 | 89842161 |
a0002 | 0/0 | 140 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | MDVFM others(135): Show |
chr4 | 89719099 | 89842161 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 420 | 336 | 81 | 64 | 148 | 10 | 33 | SNCA_chr4_89719099_89842161 | SNCA | ATGGA others(415): Show |
chr4 | 89719099 | 89842161 | ||
a0001c0002 | 0/0 | 420 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | ATGGA others(415): Show |
chr4 | 89719099 | 89842161 | ||
a0002c0003 | 0/0 | 420 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | ATGGA others(415): Show |
chr4 | 89719099 | 89842161 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3180 | 115 | 21 | 27 | 49 | 5 | 13 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0002 | 0/0 | 3178 | 105 | 12 | 13 | 72 | 0 | 8 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0003 | 0/0 | 3179 | 24 | 2 | 0 | 18 | 0 | 4 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3174): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0004 | 0/0 | 3181 | 15 | 0 | 9 | 0 | 3 | 3 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0005 | 0/0 | 3179 | 12 | 1 | 7 | 4 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3174): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0006 | 0/0 | 3177 | 7 | 7 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3172): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0007 | 0/0 | 3180 | 6 | 3 | 3 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0008 | 0/0 | 3181 | 5 | 1 | 0 | 1 | 0 | 3 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0009 | 0/0 | 3178 | 4 | 4 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0010 | 0/0 | 3177 | 4 | 0 | 2 | 0 | 2 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3172): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0011 | 0/0 | 3180 | 4 | 4 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0012 | 0/0 | 3180 | 4 | 4 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0013 | 0/0 | 3181 | 3 | 3 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0014 | 0/0 | 3181 | 3 | 3 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0015 | 0/0 | 3179 | 3 | 2 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3174): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0016 | 0/0 | 3173 | 2 | 1 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3168): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0017 | 0/0 | 3181 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0018 | 0/0 | 3179 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3174): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0019 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0020 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0021 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3172): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0022 | 0/0 | 3178 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0023 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0024 | 0/0 | 3179 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3174): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0025 | 0/0 | 3182 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3177): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0026 | 0/0 | 3173 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3168): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0027 | 0/0 | 3173 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3168): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0028 | 0/0 | 3178 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0029 | 0/0 | 3178 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0030 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0031 | 0/0 | 3182 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3177): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0032 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3169): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0033 | 0/0 | 3178 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0034 | 0/0 | 3173 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3168): Show |
chr4 | 89719099 | 89842161 |
a0001c0001t0035 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3175): Show |
chr4 | 89719099 | 89842161 |
a0001c0002t0004 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3176): Show |
chr4 | 89719099 | 89842161 |
a0002c0003t0002 | 0/0 | 3178 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | GGCGA others(3173): Show |
chr4 | 89719099 | 89842161 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0007g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0010g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0010g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0010g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0010g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0011g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0013g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0014g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0014g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0014g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0016g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0017g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0018g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0019g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0021g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0022g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0023g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0024g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0025g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0026g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0027g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0028g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0029g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0030g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0032g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0033g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0034g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0001t0035g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0001c0002t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
a0002c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0004 | g0310 | EUR | GBR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0087 | EUR | FIN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01099 | hp1 | a0001 | c0001 | t0010 | g0298 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01109 | hp2 | a0001 | c0001 | t0018 | g0016 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0143 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0304 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01243 | hp1 | a0001 | c0001 | t0016 | g0277 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01243 | hp2 | a0001 | c0001 | t0034 | g0319 | AMR | PUR | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0309 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0245 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0312 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0311 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01361 | hp1 | a0001 | c0001 | t0010 | g0297 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0305 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0294 | EUR | IBS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0300 | EUR | IBS | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01891 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02055 | hp1 | a0001 | c0001 | t0031 | g0149 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02055 | hp2 | a0001 | c0001 | t0025 | g0296 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02083 | hp1 | a0001 | c0001 | t0022 | g0264 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CDX | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02155 | hp2 | a0001 | c0001 | t0035 | g0320 | EAS | CDX | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0131 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02258 | hp2 | a0001 | c0001 | t0017 | g0244 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02280 | hp2 | a0001 | c0001 | t0016 | g0278 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PEL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0281 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0130 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0140 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0159 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02717 | hp1 | a0001 | c0001 | t0013 | g0141 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02723 | hp2 | a0001 | c0001 | t0017 | g0253 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02818 | hp1 | a0001 | c0001 | t0032 | g0252 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02896 | hp2 | a0001 | c0001 | t0024 | g0315 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0039 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0256 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02970 | hp1 | a0001 | c0001 | t0014 | g0317 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03017 | hp1 | a0001 | c0001 | t0008 | g0128 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0295 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03139 | hp2 | a0001 | c0001 | t0030 | g0227 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0282 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0242 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0160 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03516 | hp1 | a0001 | c0001 | t0026 | g0289 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0137 | AFR | ESN | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0318 | AFR | GWD | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0118 | AFR | MSL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0306 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03688 | hp2 | a0001 | c0001 | t0028 | g0046 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03942 | hp1 | a0001 | c0001 | t0033 | g0049 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0301 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0274 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18747 | hp1 | a0001 | c0001 | t0029 | g0241 | EAS | CHB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0218 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18998 | hp1 | a0001 | c0001 | t0015 | g0184 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19030 | hp2 | a0001 | c0001 | t0027 | g0101 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0248 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20129 | hp1 | a0001 | c0001 | t0019 | g0153 | AFR | ASW | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ASW | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0088 | EUR | TSI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | GIH | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0316 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0212 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | USA | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | USA | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0307 | AFR | LWK | SNCA_chr4_89719099_89842161 | SNCA | chr4 | 89719099 | 89842161 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:89822265 | T | C | 1 | a0002 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.287A>G | p.Lys96Arg | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/6 | 512/3177 | 287/423 | 96/140 | chr4 | 89822265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:89726643 | G | A | 1 | a0001c0002 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.408C>T | p.Tyr136Tyr | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 633/3177 | 408/423 | 136/140 | chr4 | 89726643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:89724520 | T | A | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(20): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*2108A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 2108 | chr4 | 89724520 | ||||||
chr4:89724522 | C | T | 1 | a0001c0001t0029 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2106G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 2106 | chr4 | 89724522 | ||||||
chr4:89724523 | C | T | 22 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(19): Show |
154 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2105G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 2105 | chr4 | 89724523 | ||||||
chr4:89724732 | G | A | 1 | a0001c0001t0030 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1896C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1896 | chr4 | 89724732 | ||||||
chr4:89724951 | G | A | 3 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0027 |
6 | HG02896.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1677C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1677 | chr4 | 89724951 | ||||||
chr4:89724955 | A | G | 1 | a0001c0001t0028 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1673T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1673 | chr4 | 89724955 | ||||||
chr4:89725318 | T | TAAA | 2 | a0001c0001t0007 a0001c0001t0023 |
7 | HG01167.hp2 HG01168.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1307_*1309dupTTT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1309 | chr4 | 89725318 | ||||||
chr4:89725318 | T | TAAAA | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(2): Show |
48 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1306_*1309dupTTTT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1309 | chr4 | 89725318 | ||||||
chr4:89725318 | T | TAAAAA | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(7): Show |
230 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1305_*1309dupTTTT others(1): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1309 | chr4 | 89725318 | ||||||
chr4:89725318 | T | TAAAAAA | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(4): Show |
32 | HG01109.hp1 HG01255.hp2 HG01978.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1304_*1309dupTTTT others(2): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1309 | chr4 | 89725318 | ||||||
chr4:89725318 | T | TAAAAAAA | 7 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0018 others(4): Show |
11 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1309dupTTTT others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1309 | chr4 | 89725318 | ||||||
chr4:89725341 | C | T | 3 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0032 |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1287G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1287 | chr4 | 89725341 | ||||||
chr4:89725350 | AAG | A | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(9): Show |
163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1276_*1277delCT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1276 | chr4 | 89725350 | ||||||
chr4:89725350 | AAGAG | A | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(16): Show |
147 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1274_*1277delCTCT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1274 | chr4 | 89725350 | ||||||
chr4:89725382 | TA | T | 3 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0024 |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1245delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1245 | chr4 | 89725382 | ||||||
chr4:89725404 | C | T | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1224 | chr4 | 89725404 | ||||||
chr4:89725535 | C | CT | 2 | a0001c0001t0013 a0001c0001t0014 |
6 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1092dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1092 | chr4 | 89725535 | ||||||
chr4:89725535 | CT | C | 5 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0017 others(2): Show |
11 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1092delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1092 | chr4 | 89725535 | ||||||
chr4:89725626 | A | C | 1 | a0001c0001t0013 | 3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1002T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 1002 | chr4 | 89725626 | ||||||
chr4:89725735 | G | A | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(3): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 893 | chr4 | 89725735 | ||||||
chr4:89725776 | C | A | 1 | a0001c0001t0018 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 852 | chr4 | 89725776 | ||||||
chr4:89725870 | A | G | 1 | a0001c0001t0022 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 758 | chr4 | 89725870 | ||||||
chr4:89725943 | T | C | 1 | a0001c0001t0034 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 685 | chr4 | 89725943 | ||||||
chr4:89726035 | G | T | 1 | a0001c0001t0021 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 593 | chr4 | 89726035 | ||||||
chr4:89726127 | G | A | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0031 others(1): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*501C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 501 | chr4 | 89726127 | ||||||
chr4:89726205 | T | C | 1 | a0001c0001t0034 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 423 | chr4 | 89726205 | ||||||
chr4:89726338 | T | C | 1 | a0001c0001t0033 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 290 | chr4 | 89726338 | ||||||
chr4:89726425 | C | T | 1 | a0001c0001t0020 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 203 | chr4 | 89726425 | ||||||
chr4:89726455 | C | T | 1 | a0001c0001t0019 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 173 | chr4 | 89726455 | ||||||
chr4:89726456 | G | A | 1 | a0001c0001t0009 | 4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 172 | chr4 | 89726456 | ||||||
chr4:89726489 | A | C | 1 | a0001c0001t0016 | 2 | HG01243.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 6/6 | 139 | chr4 | 89726489 | ||||||
chr4:89837061 | G | T | 2 | a0001c0001t0009 a0001c0001t0018 |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-125C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/6 | 1394 | chr4 | 89837061 | ||||||
chr4:89837068 | GC | G | 2 | a0001c0001t0009 a0001c0001t0018 |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-133delG | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/6 | 1402 | chr4 | 89837068 | ||||||
chr4:89837070 | C | G | 2 | a0001c0001t0009 a0001c0001t0018 |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-134G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/6 | 1403 | chr4 | 89837070 | ||||||
chr4:89837071 | G | C | 1 | a0001c0001t0034 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/6 | 1404 | chr4 | 89837071 | ||||||
chr4:89837074 | G | C | 1 | a0001c0001t0035 | 1 | HG02155.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/6 | 1407 | chr4 | 89837074 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:89726714 | T | C | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-54A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89726714 | |||||||
chr4:89726862 | C | CAGT | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-205_391-203dup others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89726862 | |||||||
chr4:89726976 | C | T | 1 | a0001c0001t0008g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.391-316G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89726976 | |||||||
chr4:89726990 | G | A | 4 | a0001c0001t0007g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-330C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89726990 | |||||||
chr4:89727034 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.391-374G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727034 | |||||||
chr4:89727192 | C | G | 2 | a0001c0001t0006g0078 a0001c0001t0006g0079 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391-532G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727192 | |||||||
chr4:89727272 | A | G | 1 | a0001c0001t0005g0270 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.391-612T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727272 | |||||||
chr4:89727441 | C | T | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391-781G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727441 | |||||||
chr4:89727535 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.391-875T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727535 | |||||||
chr4:89727581 | A | G | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-921T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727581 | |||||||
chr4:89727662 | ATGCCTGG others(85): Show |
A | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-1094_391-1003d others(94): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727662 | |||||||
chr4:89727785 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.391-1125T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89727785 | |||||||
chr4:89728112 | T | A | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.390+1082A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728112 | |||||||
chr4:89728139 | C | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
315 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.390+1055G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728139 | |||||||
chr4:89728216 | C | G | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+978G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728216 | |||||||
chr4:89728223 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0115 |
3 | HG03130.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.390+971A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728223 | |||||||
chr4:89728232 | A | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0030 others(41): Show |
45 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.390+962T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728232 | |||||||
chr4:89728364 | C | A | 1 | a0001c0001t0006g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390+830G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728364 | |||||||
chr4:89728506 | G | GT | 24 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(21): Show |
24 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(21): Show |
intron_variant | MODIFIER | c.390+687dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728506 | |||||||
chr4:89728627 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.390+567A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728627 | |||||||
chr4:89728638 | A | G | 2 | a0001c0001t0013g0140 a0001c0001t0013g0212 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.390+556T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728638 | |||||||
chr4:89728649 | T | C | 5 | a0001c0001t0011g0010 a0001c0001t0011g0118 a0001c0001t0011g0282 others(2): Show |
6 | HG02896.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+545A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89728649 | |||||||
chr4:89729103 | A | C | 5 | a0001c0001t0002g0045 a0001c0001t0002g0056 a0001c0001t0002g0237 others(2): Show |
5 | HG02074.hp2 HG02155.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+91T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89729103 | |||||||
chr4:89729158 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.390+36T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 5/5 | chr4 | 89729158 | |||||||
chr4:89729321 | G | A | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.307-44C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729321 | |||||||
chr4:89729434 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.307-157G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729434 | |||||||
chr4:89729444 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.307-167G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729444 | |||||||
chr4:89729611 | G | C | 1 | a0001c0001t0002g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.307-334C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729611 | |||||||
chr4:89729703 | T | A | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-426A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729703 | |||||||
chr4:89729705 | A | T | 1 | a0001c0001t0002g0031 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.307-428T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729705 | |||||||
chr4:89729759 | C | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-482G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729759 | |||||||
chr4:89729892 | ATTC | A | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-618_307-616del others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729892 | |||||||
chr4:89729971 | C | G | 1 | a0001c0001t0002g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.307-694G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89729971 | |||||||
chr4:89730101 | G | A | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-824C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730101 | |||||||
chr4:89730411 | C | T | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1134G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730411 | |||||||
chr4:89730710 | G | T | 5 | a0001c0001t0011g0010 a0001c0001t0011g0118 a0001c0001t0011g0282 others(2): Show |
6 | HG02896.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1433C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730710 | |||||||
chr4:89730729 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.307-1452A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730729 | |||||||
chr4:89730862 | T | C | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.307-1585A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730862 | |||||||
chr4:89730981 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.307-1704T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89730981 | |||||||
chr4:89731256 | T | A | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1979A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731256 | |||||||
chr4:89731476 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0002g0246 a0001c0001t0005g0245 |
3 | HG01106.hp1 HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.307-2199C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731476 | |||||||
chr4:89731537 | T | G | 22 | a0001c0001t0001g0109 a0001c0001t0001g0202 a0001c0001t0003g0014 others(19): Show |
23 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.307-2260A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731537 | |||||||
chr4:89731586 | C | A | 1 | a0001c0001t0003g0014 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.307-2309G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731586 | |||||||
chr4:89731643 | T | C | 1 | a0001c0001t0011g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.307-2366A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731643 | |||||||
chr4:89731923 | G | A | 6 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-2646C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731923 | |||||||
chr4:89731983 | C | T | 5 | a0001c0001t0004g0301 a0001c0001t0004g0305 a0001c0001t0004g0308 others(2): Show |
5 | HG00733.hp2 HG01496.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-2706G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731983 | |||||||
chr4:89731988 | A | G | 4 | a0001c0001t0007g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-2711T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89731988 | |||||||
chr4:89732013 | G | A | 1 | a0001c0001t0004g0301 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.307-2736C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732013 | |||||||
chr4:89732197 | C | T | 132 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(129): Show |
142 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.307-2920G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732197 | |||||||
chr4:89732329 | C | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-3052G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732329 | |||||||
chr4:89732336 | T | C | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-3059A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732336 | |||||||
chr4:89732553 | T | G | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-3276A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732553 | |||||||
chr4:89732568 | A | G | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-3291T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732568 | |||||||
chr4:89732590 | G | T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-3313C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732590 | |||||||
chr4:89732696 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.307-3419A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89732696 | |||||||
chr4:89733003 | C | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(109): Show |
121 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.307-3726G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733003 | |||||||
chr4:89733147 | G | T | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-3870C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733147 | |||||||
chr4:89733172 | TCTAA | T | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-3899_307-3896d others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733172 | |||||||
chr4:89733195 | G | A | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-3918C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733195 | |||||||
chr4:89733197 | G | C | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-3920C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733197 | |||||||
chr4:89733244 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.307-3967T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733244 | |||||||
chr4:89733513 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-4236C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733513 | |||||||
chr4:89733535 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.307-4258G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733535 | |||||||
chr4:89733852 | T | C | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-4575A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89733852 | |||||||
chr4:89734064 | G | A | 1 | a0001c0001t0014g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307-4787C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734064 | |||||||
chr4:89734079 | C | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-4802G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734079 | |||||||
chr4:89734171 | G | A | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-4894C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734171 | |||||||
chr4:89734333 | C | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-5056G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734333 | |||||||
chr4:89734345 | A | G | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.307-5068T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734345 | |||||||
chr4:89734497 | G | A | 3 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0288 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.307-5220C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734497 | |||||||
chr4:89734575 | A | AT | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-5299dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734575 | |||||||
chr4:89734611 | A | C | 1 | a0001c0001t0019g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.307-5334T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734611 | |||||||
chr4:89734823 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.307-5546C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734823 | |||||||
chr4:89734998 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-5721G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89734998 | |||||||
chr4:89735383 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.307-6106C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735383 | |||||||
chr4:89735412 | C | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-6135G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735412 | |||||||
chr4:89735620 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA19003.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.307-6343C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735620 | |||||||
chr4:89735659 | A | G | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-6382T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735659 | |||||||
chr4:89735883 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG01071.hp1 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.307-6606T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735883 | |||||||
chr4:89735889 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.307-6612C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89735889 | |||||||
chr4:89736035 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
310 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.307-6758G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736035 | |||||||
chr4:89736198 | T | C | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.307-6921A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736198 | |||||||
chr4:89736210 | TAACGAAC others(2): Show |
T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-6942_307-6934d others(11): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736210 | |||||||
chr4:89736340 | C | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-7063G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736340 | |||||||
chr4:89736401 | T | A | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-7124A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736401 | |||||||
chr4:89736414 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.307-7137A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736414 | |||||||
chr4:89736460 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.307-7183G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736460 | |||||||
chr4:89736998 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.307-7721C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89736998 | |||||||
chr4:89737006 | A | G | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-7729T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737006 | |||||||
chr4:89737106 | C | T | 3 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 |
3 | HG02486.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.307-7829G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737106 | |||||||
chr4:89737509 | C | T | 2 | a0001c0001t0012g0242 a0001c0001t0012g0248 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.307-8232G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737509 | |||||||
chr4:89737520 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.307-8243T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737520 | |||||||
chr4:89737520 | AT | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(12): Show |
15 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-8244delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737520 | |||||||
chr4:89737601 | G | A | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-8324C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737601 | |||||||
chr4:89737732 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.307-8455G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89737732 | |||||||
chr4:89738041 | A | C | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.307-8764T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738041 | |||||||
chr4:89738127 | C | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-8850G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738127 | |||||||
chr4:89738184 | A | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-8907T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738184 | |||||||
chr4:89738341 | C | A | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-9064G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738341 | |||||||
chr4:89738459 | T | C | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.307-9182A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738459 | |||||||
chr4:89738460 | C | CT | 7 | a0001c0001t0004g0089 a0001c0001t0004g0301 a0001c0001t0004g0306 others(4): Show |
7 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-9184dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | C | CTTTTT | 9 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 others(6): Show |
9 | HG00408.hp2 HG00609.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-9188_307-9184d others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | C | CTTTTTT | 7 | a0001c0001t0003g0014 a0001c0001t0003g0100 a0001c0001t0003g0102 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-9189_307-9184d others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CT | C | 35 | a0001c0001t0001g0040 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
35 | HG00597.hp1 HG00621.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.307-9184delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CTT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
119 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.307-9185_307-9184d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CTTT | C | 100 | a0001c0001t0001g0177 a0001c0001t0001g0187 a0001c0001t0001g0188 others(97): Show |
107 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.307-9186_307-9184d others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CTTTT | C | 9 | a0001c0001t0001g0095 a0001c0001t0002g0261 a0001c0001t0002g0263 others(6): Show |
10 | HG02896.hp2 HG03139.hp1 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-9187_307-9184d others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-9193_307-9184d others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738460 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.307-9200_307-9184d others(19): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738460 | |||||||
chr4:89738496 | CAG | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-9221_307-9220d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738496 | |||||||
chr4:89738534 | C | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-9257G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738534 | |||||||
chr4:89738536 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-9259G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738536 | |||||||
chr4:89738709 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-9432G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738709 | |||||||
chr4:89738753 | C | T | 4 | a0001c0001t0007g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-9476G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738753 | |||||||
chr4:89738769 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.307-9492G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738769 | |||||||
chr4:89738778 | G | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-9501C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89738778 | |||||||
chr4:89739064 | C | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-9787G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739064 | |||||||
chr4:89739138 | A | AAGAT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-9865_307-9862d others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739138 | |||||||
chr4:89739143 | A | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-9866T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739143 | |||||||
chr4:89739271 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-9994C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739271 | |||||||
chr4:89739319 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-10042G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739319 | |||||||
chr4:89739475 | C | G | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-10198G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739475 | |||||||
chr4:89739589 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-10312C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739589 | |||||||
chr4:89739867 | G | A | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-10590C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89739867 | |||||||
chr4:89740183 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.307-10906T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740183 | |||||||
chr4:89740231 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.307-10954T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740231 | |||||||
chr4:89740449 | A | T | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.307-11172T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740449 | |||||||
chr4:89740461 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-11184C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740461 | |||||||
chr4:89740500 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.307-11223A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740500 | |||||||
chr4:89740925 | TTG | T | 134 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(131): Show |
144 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.307-11650_307-1164 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740925 | |||||||
chr4:89740945 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.307-11668T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89740945 | |||||||
chr4:89741059 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-11782G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741059 | |||||||
chr4:89741516 | C | T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-12239G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741516 | |||||||
chr4:89741702 | G | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-12425C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741702 | |||||||
chr4:89741706 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.307-12429G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741706 | |||||||
chr4:89741741 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.307-12464C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741741 | |||||||
chr4:89741789 | TA | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
310 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.307-12513delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741789 | |||||||
chr4:89741844 | T | C | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307-12567A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741844 | |||||||
chr4:89741943 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.307-12666C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741943 | |||||||
chr4:89741954 | G | A | 1 | a0001c0001t0003g0014 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.307-12677C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89741954 | |||||||
chr4:89742127 | T | C | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.307-12850A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742127 | |||||||
chr4:89742168 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307-12891T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742168 | |||||||
chr4:89742391 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-13114A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742391 | |||||||
chr4:89742423 | G | T | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.307-13146C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742423 | |||||||
chr4:89742519 | T | G | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-13242A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742519 | |||||||
chr4:89742521 | C | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-13244G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742521 | |||||||
chr4:89742991 | TA | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-13715delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89742991 | |||||||
chr4:89743201 | T | C | 5 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0062 others(2): Show |
5 | NA18747.hp2 NA18986.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-13924A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743201 | |||||||
chr4:89743308 | A | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-14031T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743308 | |||||||
chr4:89743327 | A | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-14050T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743327 | |||||||
chr4:89743331 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-14054A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743331 | |||||||
chr4:89743643 | C | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-14366G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743643 | |||||||
chr4:89743684 | A | G | 3 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 |
3 | HG02486.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.307-14407T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743684 | |||||||
chr4:89743922 | G | C | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-14645C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743922 | |||||||
chr4:89743941 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-14664A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89743941 | |||||||
chr4:89744105 | C | T | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(109): Show |
121 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.307-14828G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89744105 | |||||||
chr4:89744340 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.307-15063C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89744340 | |||||||
chr4:89744355 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.307-15078C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89744355 | |||||||
chr4:89744512 | C | T | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-15235G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89744512 | |||||||
chr4:89744890 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.307-15613G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89744890 | |||||||
chr4:89745101 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-15824G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89745101 | |||||||
chr4:89745140 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(284): Show |
304 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.307-15863C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89745140 | |||||||
chr4:89745554 | TACTC | T | 137 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(134): Show |
147 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.307-16281_307-1627 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89745554 | |||||||
chr4:89745606 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.307-16329G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89745606 | |||||||
chr4:89745705 | T | G | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-16428A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89745705 | |||||||
chr4:89746207 | T | C | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.307-16930A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746207 | |||||||
chr4:89746212 | A | G | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.307-16935T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746212 | |||||||
chr4:89746496 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.307-17219A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746496 | |||||||
chr4:89746861 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0220 |
2 | HG00673.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.307-17584T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746861 | |||||||
chr4:89746868 | A | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-17591T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746868 | |||||||
chr4:89746894 | C | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-17617G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89746894 | |||||||
chr4:89747023 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.307-17746T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747023 | |||||||
chr4:89747033 | T | A | 1 | a0001c0001t0002g0048 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.307-17756A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747033 | |||||||
chr4:89747114 | A | G | 6 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-17837T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747114 | |||||||
chr4:89747150 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0220 |
2 | HG00673.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.307-17873C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747150 | |||||||
chr4:89747225 | C | T | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-17948G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747225 | |||||||
chr4:89747236 | G | GCA | 44 | a0001c0001t0001g0085 a0001c0001t0001g0132 a0001c0001t0001g0136 others(41): Show |
46 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-17961_307-1796 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747236 | |||||||
chr4:89747236 | G | GCGCACAC others(1): Show |
6 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0206 others(3): Show |
6 | HG02809.hp2 HG02818.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-17960_307-1795 others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747236 | |||||||
chr4:89747236 | G | GCGCACAC others(3): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 |
3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.307-17960_307-1795 others(14): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747236 | |||||||
chr4:89747236 | G | GCGCACAC others(5): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0192 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.307-17960_307-1795 others(16): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747236 | |||||||
chr4:89747236 | G | GCGCACAC others(7): Show |
1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.307-17960_307-1795 others(18): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747236 | |||||||
chr4:89747238 | A | G | 1 | a0001c0001t0014g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307-17961T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747238 | |||||||
chr4:89747260 | ACACACAC others(1): Show |
A | 9 | a0001c0001t0005g0279 a0001c0001t0012g0242 a0001c0001t0012g0248 others(6): Show |
9 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-17991_307-1798 others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747260 | |||||||
chr4:89747264 | ACACC | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0028 a0001c0001t0002g0066 others(1): Show |
5 | HG02559.hp2 HG02895.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-17991_307-1798 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747264 | |||||||
chr4:89747266 | ACC | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0123 others(111): Show |
120 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.307-17991_307-1799 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747266 | |||||||
chr4:89747268 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.307-17991G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747268 | |||||||
chr4:89747325 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.307-18048C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747325 | |||||||
chr4:89747449 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-18172G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747449 | |||||||
chr4:89747463 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-18186A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747463 | |||||||
chr4:89747659 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-18382G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747659 | |||||||
chr4:89747703 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-18426C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747703 | |||||||
chr4:89747782 | T | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.307-18505A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747782 | |||||||
chr4:89747863 | G | A | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-18586C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747863 | |||||||
chr4:89747889 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.307-18612G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89747889 | |||||||
chr4:89748039 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.307-18762C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748039 | |||||||
chr4:89748194 | TA | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
10 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-18918delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748194 | |||||||
chr4:89748457 | T | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-19180A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748457 | |||||||
chr4:89748472 | C | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0223 others(6): Show |
13 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.307-19195G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748472 | |||||||
chr4:89748499 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-19222G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748499 | |||||||
chr4:89748604 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-19327G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748604 | |||||||
chr4:89748760 | G | A | 3 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0021g0039 |
3 | HG02965.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.307-19483C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748760 | |||||||
chr4:89748826 | A | ATTTCCAC others(10): Show |
2 | a0001c0001t0004g0303 a0001c0001t0007g0304 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.307-19566_307-1955 others(21): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748826 | |||||||
chr4:89748969 | G | A | 3 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 |
3 | HG02486.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.307-19692C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89748969 | |||||||
chr4:89749217 | G | C | 1 | a0001c0001t0017g0244 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.307-19940C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749217 | |||||||
chr4:89749765 | C | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-20488G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749765 | |||||||
chr4:89749899 | TATGTG | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-20627_307-2062 others(9): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749899 | |||||||
chr4:89749900 | A | ATG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
120 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.307-20625_307-2062 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749900 | |||||||
chr4:89749900 | ATG | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(51): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.307-20625_307-2062 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749900 | |||||||
chr4:89749914 | GTGTATAT others(29): Show |
G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0254 a0001c0001t0002g0260 |
3 | NA19081.hp2 NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.307-20673_307-2063 others(40): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749914 | |||||||
chr4:89749918 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0081 others(12): Show |
16 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.307-20641T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749918 | |||||||
chr4:89749939 | G | GAT | 45 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0040 others(42): Show |
46 | HG00639.hp1 HG00741.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-20664_307-2066 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | G | GATAT | 6 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0123 others(3): Show |
6 | HG00558.hp1 HG00733.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-20666_307-2066 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | G | GATATAT | 22 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0092 others(19): Show |
24 | HG00408.hp2 HG00609.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.307-20668_307-2066 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | G | GATATATA others(1): Show |
3 | a0001c0001t0001g0091 a0001c0001t0003g0107 a0001c0001t0034g0319 |
3 | HG01243.hp2 HG01928.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.307-20670_307-2066 others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | G | GATATATA others(5): Show |
1 | a0001c0001t0001g0008 | 2 | HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.307-20674_307-2066 others(16): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | GATATAT | G | 22 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(19): Show |
23 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-20668_307-2066 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749939 | GATATATA others(3): Show |
G | 111 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(108): Show |
120 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.307-20672_307-2066 others(14): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749939 | |||||||
chr4:89749947 | T | G | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-20670A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749947 | |||||||
chr4:89749949 | T | G | 22 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(19): Show |
23 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-20672A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749949 | |||||||
chr4:89749973 | G | GAT | 110 | a0001c0001t0001g0115 a0001c0001t0002g0002 a0001c0001t0002g0003 others(107): Show |
119 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.307-20698_307-2069 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89749973 | |||||||
chr4:89750136 | A | G | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-20859T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750136 | |||||||
chr4:89750185 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-20908C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750185 | |||||||
chr4:89750231 | C | A | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-20954G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750231 | |||||||
chr4:89750238 | CT | C | 159 | a0001c0001t0001g0109 a0001c0001t0002g0002 a0001c0001t0002g0003 others(156): Show |
170 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.307-20962delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750238 | |||||||
chr4:89750336 | G | A | 137 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(134): Show |
147 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.307-21059C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750336 | |||||||
chr4:89750371 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-21094G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750371 | |||||||
chr4:89750398 | A | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-21121T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750398 | |||||||
chr4:89750401 | C | T | 1 | a0001c0001t0028g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.307-21124G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750401 | |||||||
chr4:89750519 | A | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
315 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.307-21242T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750519 | |||||||
chr4:89750634 | C | T | 1 | a0001c0001t0009g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.307-21357G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750634 | |||||||
chr4:89750837 | C | A | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-21560G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750837 | |||||||
chr4:89750927 | A | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-21650T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89750927 | |||||||
chr4:89751002 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.307-21725T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751002 | |||||||
chr4:89751135 | C | T | 2 | a0001c0001t0008g0159 a0001c0001t0008g0160 |
2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.307-21858G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751135 | |||||||
chr4:89751139 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0066 a0001c0001t0002g0074 |
4 | HG02559.hp2 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-21862A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751139 | |||||||
chr4:89751173 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.307-21896G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751173 | |||||||
chr4:89751296 | GA | G | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-22020delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751296 | |||||||
chr4:89751297 | AT | A | 4 | a0001c0001t0001g0200 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG01099.hp2 HG01884.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-22021delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751297 | |||||||
chr4:89751305 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0002g0291 a0001c0001t0003g0107 |
3 | HG02602.hp2 NA19074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.307-22028A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751305 | |||||||
chr4:89751306 | A | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(15): Show |
18 | HG00597.hp1 HG02004.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.307-22029T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751306 | |||||||
chr4:89751321 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307-22044G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751321 | |||||||
chr4:89751324 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.307-22047T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751324 | |||||||
chr4:89751373 | C | CTCTT | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-22097_307-2209 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751373 | |||||||
chr4:89751403 | T | C | 6 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-22126A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751403 | |||||||
chr4:89751419 | T | C | 1 | a0001c0001t0003g0014 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.307-22142A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751419 | |||||||
chr4:89751504 | A | G | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-22227T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751504 | |||||||
chr4:89751783 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.307-22506A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751783 | |||||||
chr4:89751809 | T | C | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-22532A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751809 | |||||||
chr4:89751845 | G | GA | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-22569dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89751845 | |||||||
chr4:89752054 | A | C | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.307-22777T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752054 | |||||||
chr4:89752534 | T | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.307-23257A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752534 | |||||||
chr4:89752607 | G | GTTC | 99 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(96): Show |
107 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.307-23333_307-2333 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752607 | |||||||
chr4:89752607 | G | GTTCTTC | 15 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0041 others(12): Show |
15 | HG01928.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-23336_307-2333 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752607 | |||||||
chr4:89752610 | C | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.307-23333G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752610 | |||||||
chr4:89752616 | CTTA | C | 99 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(96): Show |
107 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.307-23342_307-2334 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752616 | |||||||
chr4:89752616 | CTTATTA | C | 15 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0041 others(12): Show |
15 | HG01928.hp1 HG02602.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-23345_307-2334 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752616 | |||||||
chr4:89752619 | A | C | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-23342T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752619 | |||||||
chr4:89752619 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
182 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.307-23342T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752619 | |||||||
chr4:89752622 | A | C | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-23345T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752622 | |||||||
chr4:89752634 | A | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-23357T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752634 | |||||||
chr4:89752690 | A | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-23413T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752690 | |||||||
chr4:89752867 | A | C | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-23590T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752867 | |||||||
chr4:89752904 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0167 a0001c0001t0001g0219 others(1): Show |
4 | HG00673.hp2 HG01928.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-23627G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89752904 | |||||||
chr4:89753079 | G | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-23802C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89753079 | |||||||
chr4:89753280 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-24003C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89753280 | |||||||
chr4:89753300 | T | C | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-24023A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89753300 | |||||||
chr4:89754025 | T | C | 1 | a0001c0001t0002g0012 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.307-24748A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754025 | |||||||
chr4:89754087 | A | G | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(142): Show |
155 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.307-24810T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754087 | |||||||
chr4:89754106 | T | G | 1 | a0001c0001t0019g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.307-24829A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754106 | |||||||
chr4:89754167 | A | G | 4 | a0001c0001t0007g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-24890T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754167 | |||||||
chr4:89754467 | T | C | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-25190A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754467 | |||||||
chr4:89754510 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-25233G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754510 | |||||||
chr4:89754742 | C | T | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-25465G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754742 | |||||||
chr4:89754858 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-25581T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89754858 | |||||||
chr4:89755254 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.307-25977T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755254 | |||||||
chr4:89755407 | A | AG | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-26131dupC | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755407 | |||||||
chr4:89755409 | G | C | 20 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.307-26132C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755409 | |||||||
chr4:89755693 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-26416A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755693 | |||||||
chr4:89755697 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.307-26420T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755697 | |||||||
chr4:89755778 | C | CT | 254 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
270 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.307-26502dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755778 | |||||||
chr4:89755778 | C | CTT | 10 | a0001c0001t0001g0180 a0001c0001t0001g0196 a0001c0001t0002g0062 others(7): Show |
10 | HG00140.hp2 HG01070.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-26503_307-2650 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755778 | |||||||
chr4:89755782 | T | C | 2 | a0001c0001t0004g0015 a0001c0001t0007g0312 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.307-26505A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755782 | |||||||
chr4:89755864 | C | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-26587G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755864 | |||||||
chr4:89755940 | G | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-26663C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755940 | |||||||
chr4:89755997 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
310 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.307-26720A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89755997 | |||||||
chr4:89756047 | G | A | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-26770C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756047 | |||||||
chr4:89756092 | G | A | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-26815C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756092 | |||||||
chr4:89756295 | G | A | 2 | a0001c0001t0004g0303 a0001c0001t0007g0304 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.307-27018C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756295 | |||||||
chr4:89756380 | T | C | 21 | a0001c0001t0001g0109 a0001c0001t0003g0014 a0001c0001t0003g0096 others(18): Show |
22 | HG00408.hp2 HG00609.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-27103A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756380 | |||||||
chr4:89756650 | T | C | 8 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-27373A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756650 | |||||||
chr4:89756769 | C | A | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-27492G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756769 | |||||||
chr4:89756799 | GACTATAA others(3): Show |
G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-27532_307-2752 others(14): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89756799 | |||||||
chr4:89757028 | C | G | 1 | a0001c0001t0002g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.307-27751G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757028 | |||||||
chr4:89757103 | A | ATTT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
7 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-27827_307-2782 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757103 | |||||||
chr4:89757104 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
7 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-27827C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757104 | |||||||
chr4:89757104 | G | GTTA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
106 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.307-27830_307-2782 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757104 | |||||||
chr4:89757162 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.307-27885A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757162 | |||||||
chr4:89757182 | T | C | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-27905A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757182 | |||||||
chr4:89757318 | C | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.307-28041G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757318 | |||||||
chr4:89757390 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
113 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.307-28113C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757390 | |||||||
chr4:89757647 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
310 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.307-28370C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757647 | |||||||
chr4:89757730 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.307-28453C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757730 | |||||||
chr4:89757933 | A | G | 1 | a0001c0001t0002g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.307-28656T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89757933 | |||||||
chr4:89758095 | T | C | 7 | a0001c0001t0012g0248 a0001c0001t0012g0256 a0001c0001t0012g0281 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-28818A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758095 | |||||||
chr4:89758104 | G | A | 8 | a0001c0001t0001g0109 a0001c0001t0012g0248 a0001c0001t0012g0256 others(5): Show |
8 | HG02055.hp1 HG02135.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.307-28827C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758104 | |||||||
chr4:89758160 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.307-28883A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758160 | |||||||
chr4:89758201 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.307-28924T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758201 | |||||||
chr4:89758324 | T | G | 22 | a0001c0001t0002g0006 a0001c0001t0002g0030 a0001c0001t0002g0047 others(19): Show |
23 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-29047A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758324 | |||||||
chr4:89758349 | C | T | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-29072G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758349 | |||||||
chr4:89758377 | G | A | 9 | a0001c0001t0001g0109 a0001c0001t0012g0242 a0001c0001t0012g0248 others(6): Show |
9 | HG02055.hp1 HG02135.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.307-29100C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758377 | |||||||
chr4:89758662 | T | C | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-29385A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758662 | |||||||
chr4:89758753 | G | A | 4 | a0001c0001t0007g0134 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-29476C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758753 | |||||||
chr4:89758869 | C | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-29592G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758869 | |||||||
chr4:89758913 | T | C | 2 | a0001c0001t0002g0005 a0001c0001t0002g0027 |
3 | HG02723.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.307-29636A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89758913 | |||||||
chr4:89759298 | C | CA | 22 | a0001c0001t0001g0185 a0001c0001t0002g0284 a0001c0001t0002g0285 others(19): Show |
22 | HG01099.hp2 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.307-30022dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759298 | |||||||
chr4:89759312 | A | AG | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-30036_307-3003 others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759312 | |||||||
chr4:89759478 | A | ATGCATAT others(1): Show |
136 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(133): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.307-30202_307-3020 others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759478 | |||||||
chr4:89759484 | C | T | 7 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(4): Show |
7 | HG01099.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-30207G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759484 | |||||||
chr4:89759822 | CT | C | 129 | a0001c0001t0001g0169 a0001c0001t0001g0199 a0001c0001t0001g0222 others(126): Show |
139 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.307-30546delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759822 | |||||||
chr4:89759830 | T | TG | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-30554_307-3055 others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759830 | |||||||
chr4:89759845 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.307-30568G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89759845 | |||||||
chr4:89760085 | A | C | 6 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-30808T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760085 | |||||||
chr4:89760242 | T | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-30965A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760242 | |||||||
chr4:89760262 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.307-30985T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760262 | |||||||
chr4:89760642 | GA | G | 11 | a0001c0001t0002g0226 a0001c0001t0002g0228 a0001c0001t0002g0229 others(8): Show |
11 | HG00408.hp1 HG00621.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-31366delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760642 | |||||||
chr4:89760878 | T | C | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-31601A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760878 | |||||||
chr4:89760967 | T | G | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-31690A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89760967 | |||||||
chr4:89761079 | G | A | 1 | a0001c0001t0002g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.307-31802C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761079 | |||||||
chr4:89761113 | C | A | 1 | a0001c0001t0019g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.307-31836G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761113 | |||||||
chr4:89761176 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(282): Show |
301 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.307-31899C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761176 | |||||||
chr4:89761323 | T | C | 139 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(136): Show |
148 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.307-32046A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761323 | |||||||
chr4:89761353 | C | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
46 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.307-32076G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761353 | |||||||
chr4:89761420 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(101): Show |
107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.307-32143T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761420 | |||||||
chr4:89761482 | T | C | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-32205A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761482 | |||||||
chr4:89761599 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
46 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.307-32322C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761599 | |||||||
chr4:89761614 | G | A | 1 | a0001c0001t0014g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307-32337C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761614 | |||||||
chr4:89761652 | A | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
46 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.307-32375T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761652 | |||||||
chr4:89761737 | G | T | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.307-32460C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761737 | |||||||
chr4:89761829 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.307-32552C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89761829 | |||||||
chr4:89762017 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(296): Show |
315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.307-32740A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762017 | |||||||
chr4:89762097 | G | A | 1 | a0001c0001t0004g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.307-32820C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762097 | |||||||
chr4:89762124 | T | C | 1 | a0001c0001t0019g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.307-32847A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762124 | |||||||
chr4:89762158 | G | C | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-32881C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762158 | |||||||
chr4:89762518 | G | T | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-33241C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762518 | |||||||
chr4:89762554 | C | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-33277G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762554 | |||||||
chr4:89762555 | G | A | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-33278C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762555 | |||||||
chr4:89762643 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.307-33366G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762643 | |||||||
chr4:89762680 | G | A | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-33403C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762680 | |||||||
chr4:89762839 | T | C | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-33562A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762839 | |||||||
chr4:89762903 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.307-33626G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762903 | |||||||
chr4:89762971 | A | G | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-33694T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762971 | |||||||
chr4:89762972 | A | G | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-33695T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89762972 | |||||||
chr4:89763127 | A | G | 115 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(112): Show |
124 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.307-33850T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763127 | |||||||
chr4:89763212 | A | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-33935T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763212 | |||||||
chr4:89763542 | G | A | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.307-34265C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763542 | |||||||
chr4:89763615 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.307-34338T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763615 | |||||||
chr4:89763892 | A | G | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307-34615T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763892 | |||||||
chr4:89763948 | G | A | 2 | a0001c0001t0014g0318 a0001c0001t0024g0315 |
2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.307-34671C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89763948 | |||||||
chr4:89764184 | G | C | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.307-34907C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764184 | |||||||
chr4:89764431 | AT | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(265): Show |
284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.307-35155delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764431 | |||||||
chr4:89764431 | ATT | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0156 a0001c0001t0001g0161 others(18): Show |
21 | HG01167.hp2 HG01243.hp1 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.307-35156_307-3515 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764431 | |||||||
chr4:89764433 | T | C | 7 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-35156A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764433 | |||||||
chr4:89764463 | G | C | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-35186C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764463 | |||||||
chr4:89764481 | G | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
43 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.307-35204C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764481 | |||||||
chr4:89764485 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.307-35208C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764485 | |||||||
chr4:89764647 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-35370T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764647 | |||||||
chr4:89764652 | C | T | 1 | a0001c0001t0009g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.307-35375G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764652 | |||||||
chr4:89764655 | TCTC | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-35381_307-3537 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764655 | |||||||
chr4:89764667 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-35390T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764667 | |||||||
chr4:89764677 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0192 |
2 | HG02717.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.307-35400G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764677 | |||||||
chr4:89764721 | A | G | 2 | a0001c0001t0014g0316 a0001c0001t0014g0317 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.307-35444T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764721 | |||||||
chr4:89764828 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0097 |
4 | HG00558.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-35551G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764828 | |||||||
chr4:89764982 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 |
3 | HG00741.hp2 HG01258.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.307-35705A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764982 | |||||||
chr4:89764996 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0033g0049 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.307-35719A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89764996 | |||||||
chr4:89765081 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0003g0178 |
2 | HG01517.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.307-35804T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765081 | |||||||
chr4:89765324 | A | G | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-36047T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765324 | |||||||
chr4:89765548 | T | C | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.307-36271A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765548 | |||||||
chr4:89765591 | A | G | 138 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(135): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-36314T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765591 | |||||||
chr4:89765696 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.307-36419A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765696 | |||||||
chr4:89765759 | G | A | 1 | a0001c0001t0006g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307-36482C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765759 | |||||||
chr4:89765774 | T | C | 43 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0030 others(40): Show |
44 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.307-36497A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765774 | |||||||
chr4:89765907 | C | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-36630G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765907 | |||||||
chr4:89765949 | T | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-36672A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765949 | |||||||
chr4:89765968 | G | A | 111 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(108): Show |
119 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.307-36691C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765968 | |||||||
chr4:89765983 | C | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-36706G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89765983 | |||||||
chr4:89766071 | A | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.307-36794T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766071 | |||||||
chr4:89766356 | C | T | 111 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(108): Show |
119 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.307-37079G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766356 | |||||||
chr4:89766408 | G | T | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.307-37131C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766408 | |||||||
chr4:89766711 | G | A | 132 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(129): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-37434C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766711 | |||||||
chr4:89766776 | G | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-37499C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766776 | |||||||
chr4:89766969 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
64 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.307-37692C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89766969 | |||||||
chr4:89767045 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.307-37768T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767045 | |||||||
chr4:89767194 | G | C | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.307-37917C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767194 | |||||||
chr4:89767289 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.307-38012A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767289 | |||||||
chr4:89767406 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.307-38129C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767406 | |||||||
chr4:89767425 | CCT | C | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-38150_307-3814 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767425 | |||||||
chr4:89767534 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.307-38257G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767534 | |||||||
chr4:89767765 | C | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-38488G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767765 | |||||||
chr4:89767979 | A | G | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.307-38702T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89767979 | |||||||
chr4:89768300 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.307-39023T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89768300 | |||||||
chr4:89768920 | C | A | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
139 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.307-39643G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89768920 | |||||||
chr4:89768985 | C | T | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-39708G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89768985 | |||||||
chr4:89769178 | C | T | 137 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(134): Show |
145 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.307-39901G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769178 | |||||||
chr4:89769201 | G | A | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.307-39924C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769201 | |||||||
chr4:89769209 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.307-39932A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769209 | |||||||
chr4:89769210 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.307-39933C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769210 | |||||||
chr4:89769212 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.307-39935A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769212 | |||||||
chr4:89769553 | T | C | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
139 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.307-40276A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769553 | |||||||
chr4:89769569 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.307-40292G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769569 | |||||||
chr4:89769597 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(68): Show |
74 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.307-40320G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769597 | |||||||
chr4:89769681 | A | G | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
139 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.307-40404T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769681 | |||||||
chr4:89769748 | T | C | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-40471A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769748 | |||||||
chr4:89769780 | A | G | 132 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(129): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-40503T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769780 | |||||||
chr4:89769787 | C | T | 16 | a0001c0001t0002g0012 a0001c0001t0002g0226 a0001c0001t0002g0228 others(13): Show |
17 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.307-40510G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769787 | |||||||
chr4:89769788 | G | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-40511C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769788 | |||||||
chr4:89769788 | G | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-40511C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769788 | |||||||
chr4:89769901 | T | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0271 a0001c0001t0002g0272 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-40624A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769901 | |||||||
chr4:89769914 | G | A | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-40637C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769914 | |||||||
chr4:89769981 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-40704A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89769981 | |||||||
chr4:89770311 | A | C | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-41034T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89770311 | |||||||
chr4:89770386 | T | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
61 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.307-41109A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89770386 | |||||||
chr4:89770710 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.307-41433T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89770710 | |||||||
chr4:89770747 | C | T | 2 | a0001c0001t0012g0242 a0001c0001t0012g0248 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.307-41470G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89770747 | |||||||
chr4:89771016 | T | A | 1 | a0001c0001t0007g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.307-41739A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771016 | |||||||
chr4:89771185 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.307-41908G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771185 | |||||||
chr4:89771317 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-42040A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771317 | |||||||
chr4:89771534 | CT | C | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-42258delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771534 | |||||||
chr4:89771707 | T | C | 1 | a0001c0001t0008g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.307-42430A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771707 | |||||||
chr4:89771752 | C | A | 1 | a0001c0001t0029g0241 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.307-42475G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771752 | |||||||
chr4:89771758 | C | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-42481G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771758 | |||||||
chr4:89771923 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.307-42646T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771923 | |||||||
chr4:89771935 | C | T | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-42658G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89771935 | |||||||
chr4:89772040 | T | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-42763A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772040 | |||||||
chr4:89772325 | C | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0077 others(20): Show |
25 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.307-43048G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772325 | |||||||
chr4:89772348 | A | C | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-43071T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772348 | |||||||
chr4:89772413 | T | G | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-43136A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772413 | |||||||
chr4:89772506 | CT | C | 133 | a0001c0001t0001g0085 a0001c0001t0001g0199 a0001c0001t0001g0251 others(130): Show |
141 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.307-43230delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772506 | |||||||
chr4:89772596 | G | A | 2 | a0001c0001t0004g0303 a0001c0001t0007g0304 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.307-43319C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772596 | |||||||
chr4:89772664 | GGCTATT | G | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-43393_307-4338 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772664 | |||||||
chr4:89772668 | A | AT | 17 | a0001c0001t0002g0012 a0001c0001t0002g0226 a0001c0001t0002g0228 others(14): Show |
18 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-43392dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772668 | |||||||
chr4:89772668 | AT | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(169): Show |
179 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.307-43392delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772668 | |||||||
chr4:89772672 | T | A | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-43395A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89772672 | |||||||
chr4:89773140 | T | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-43863A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773140 | |||||||
chr4:89773152 | TATA | T | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-43878_307-4387 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773152 | |||||||
chr4:89773177 | C | T | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-43900G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773177 | |||||||
chr4:89773226 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0097 |
4 | HG00558.hp1 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-43949C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773226 | |||||||
chr4:89773346 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA19003.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.307-44069T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773346 | |||||||
chr4:89773387 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.307-44110A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773387 | |||||||
chr4:89773424 | T | A | 1 | a0001c0001t0002g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.307-44147A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773424 | |||||||
chr4:89773436 | T | G | 131 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(128): Show |
139 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.307-44159A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773436 | |||||||
chr4:89773460 | C | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-44183G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773460 | |||||||
chr4:89773540 | G | T | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-44263C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773540 | |||||||
chr4:89773561 | A | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0112 |
2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.307-44284T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773561 | |||||||
chr4:89773908 | G | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-44631C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89773908 | |||||||
chr4:89774119 | A | G | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-44842T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774119 | |||||||
chr4:89774357 | G | A | 126 | a0001c0001t0001g0251 a0001c0001t0002g0002 a0001c0001t0002g0003 others(123): Show |
134 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.307-45080C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774357 | |||||||
chr4:89774371 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.307-45094G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774371 | |||||||
chr4:89774638 | T | C | 1 | a0001c0001t0012g0248 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.307-45361A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774638 | |||||||
chr4:89774655 | G | A | 1 | a0001c0001t0004g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.307-45378C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774655 | |||||||
chr4:89774709 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.307-45432A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774709 | |||||||
chr4:89774885 | T | C | 132 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(129): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.307-45608A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774885 | |||||||
chr4:89774925 | A | T | 2 | a0001c0001t0014g0316 a0001c0001t0014g0317 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.307-45648T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774925 | |||||||
chr4:89774926 | T | C | 1 | a0001c0001t0003g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.307-45649A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89774926 | |||||||
chr4:89775030 | C | A | 2 | a0001c0001t0001g0280 a0001c0001t0005g0270 |
2 | HG02132.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.307-45753G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775030 | |||||||
chr4:89775042 | T | C | 1 | a0001c0001t0004g0301 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.307-45765A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775042 | |||||||
chr4:89775184 | A | G | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-45907T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775184 | |||||||
chr4:89775408 | C | A | 1 | a0001c0001t0002g0275 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.307-46131G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775408 | |||||||
chr4:89775574 | T | C | 1 | a0001c0001t0015g0184 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.307-46297A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775574 | |||||||
chr4:89775601 | C | A | 7 | a0001c0001t0007g0142 a0001c0001t0012g0242 a0001c0001t0012g0248 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-46324G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775601 | |||||||
chr4:89775676 | A | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.307-46399T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775676 | |||||||
chr4:89775692 | C | T | 1 | a0001c0001t0008g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.307-46415G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775692 | |||||||
chr4:89775978 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+46268A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89775978 | |||||||
chr4:89776006 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
63 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.306+46240A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776006 | |||||||
chr4:89776275 | C | T | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.306+45971G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776275 | |||||||
chr4:89776315 | T | C | 134 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(131): Show |
143 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.306+45931A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776315 | |||||||
chr4:89776402 | T | C | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+45844A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776402 | |||||||
chr4:89776444 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0027 |
4 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+45802C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776444 | |||||||
chr4:89776460 | A | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0219 a0001c0001t0003g0151 |
3 | HG00673.hp2 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.306+45786T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776460 | |||||||
chr4:89776510 | C | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.306+45736G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776510 | |||||||
chr4:89776575 | G | C | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+45671C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776575 | |||||||
chr4:89776788 | T | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+45458A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776788 | |||||||
chr4:89776828 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
63 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.306+45418A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776828 | |||||||
chr4:89776860 | A | G | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+45386T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89776860 | |||||||
chr4:89777335 | C | T | 6 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 others(3): Show |
6 | HG01099.hp2 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+44911G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777335 | |||||||
chr4:89777519 | C | T | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+44727G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777519 | |||||||
chr4:89777644 | G | A | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.306+44602C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777644 | |||||||
chr4:89777692 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.306+44554G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777692 | |||||||
chr4:89777693 | G | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+44553C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777693 | |||||||
chr4:89777810 | C | T | 6 | a0001c0001t0003g0105 a0001c0001t0009g0017 a0001c0001t0009g0018 others(3): Show |
6 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+44436G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777810 | |||||||
chr4:89777813 | G | T | 112 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(109): Show |
120 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.306+44433C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777813 | |||||||
chr4:89777844 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.306+44402C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777844 | |||||||
chr4:89777886 | C | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+44360G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89777886 | |||||||
chr4:89778146 | G | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+44100C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778146 | |||||||
chr4:89778166 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.306+44080G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778166 | |||||||
chr4:89778465 | C | A | 1 | a0001c0001t0001g0008 | 2 | HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.306+43781G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778465 | |||||||
chr4:89778628 | T | C | 112 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(109): Show |
120 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.306+43618A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778628 | |||||||
chr4:89778844 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.306+43402G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778844 | |||||||
chr4:89778945 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.306+43301C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89778945 | |||||||
chr4:89779010 | C | G | 141 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(138): Show |
150 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.306+43236G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779010 | |||||||
chr4:89779085 | T | C | 1 | a0001c0001t0002g0291 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.306+43161A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779085 | |||||||
chr4:89779178 | T | C | 5 | a0001c0001t0004g0015 a0001c0001t0004g0309 a0001c0001t0004g0310 others(2): Show |
6 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+43068A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779178 | |||||||
chr4:89779200 | C | CA | 6 | a0001c0001t0006g0033 a0001c0001t0012g0242 a0001c0001t0012g0248 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+43045dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779200 | |||||||
chr4:89779476 | C | A | 1 | a0001c0001t0002g0292 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.306+42770G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779476 | |||||||
chr4:89779658 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.306+42588G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779658 | |||||||
chr4:89779800 | A | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+42446T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89779800 | |||||||
chr4:89780008 | C | A | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+42238G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780008 | |||||||
chr4:89780061 | C | T | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+42185G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780061 | |||||||
chr4:89780199 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+42047T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780199 | |||||||
chr4:89780291 | A | G | 141 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(138): Show |
150 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.306+41955T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780291 | |||||||
chr4:89780293 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0012g0281 a0001c0001t0034g0319 |
4 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+41953G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780293 | |||||||
chr4:89780392 | A | G | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.306+41854T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780392 | |||||||
chr4:89780397 | T | A | 1 | a0001c0001t0006g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+41849A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780397 | |||||||
chr4:89780423 | G | A | 6 | a0001c0001t0012g0242 a0001c0001t0012g0248 a0001c0001t0012g0256 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+41823C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780423 | |||||||
chr4:89780439 | G | A | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+41807C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780439 | |||||||
chr4:89780518 | T | C | 3 | a0001c0001t0015g0129 a0001c0001t0015g0130 a0001c0001t0020g0131 |
3 | HG01891.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+41728A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780518 | |||||||
chr4:89780954 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.306+41292G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780954 | |||||||
chr4:89780995 | G | A | 141 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(138): Show |
150 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.306+41251C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89780995 | |||||||
chr4:89781385 | C | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+40861G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781385 | |||||||
chr4:89781432 | G | C | 2 | a0001c0001t0011g0282 a0001c0001t0030g0227 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.306+40814C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781432 | |||||||
chr4:89781481 | T | G | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+40765A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781481 | |||||||
chr4:89781630 | A | G | 142 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(139): Show |
151 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.306+40616T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781630 | |||||||
chr4:89781679 | ACT | A | 3 | a0001c0001t0002g0013 a0001c0001t0012g0281 a0001c0001t0034g0319 |
4 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+40565_306+4056 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781679 | |||||||
chr4:89781854 | C | T | 3 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.306+40392G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781854 | |||||||
chr4:89781878 | A | G | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+40368T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89781878 | |||||||
chr4:89782014 | T | A | 3 | a0001c0001t0002g0013 a0001c0001t0012g0281 a0001c0001t0034g0319 |
4 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+40232A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782014 | |||||||
chr4:89782082 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
309 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.306+40164T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782082 | |||||||
chr4:89782151 | T | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+40095A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782151 | |||||||
chr4:89782395 | T | C | 1 | a0001c0001t0005g0232 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.306+39851A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782395 | |||||||
chr4:89782425 | ATTG | A | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+39818_306+3982 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782425 | |||||||
chr4:89782455 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.306+39791A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782455 | |||||||
chr4:89782468 | T | G | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+39778A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782468 | |||||||
chr4:89782524 | A | G | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+39722T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782524 | |||||||
chr4:89782602 | T | C | 85 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(82): Show |
89 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.306+39644A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782602 | |||||||
chr4:89782674 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.306+39572A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782674 | |||||||
chr4:89782842 | C | A | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+39404G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782842 | |||||||
chr4:89782860 | G | A | 142 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(139): Show |
151 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.306+39386C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782860 | |||||||
chr4:89782993 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0008g0218 |
2 | NA18949.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.306+39253G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89782993 | |||||||
chr4:89783197 | C | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG00597.hp1 HG02004.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+39049G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783197 | |||||||
chr4:89783250 | T | C | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+38996A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783250 | |||||||
chr4:89783282 | A | G | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+38964T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783282 | |||||||
chr4:89783330 | G | A | 1 | a0001c0001t0020g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306+38916C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783330 | |||||||
chr4:89783404 | G | A | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+38842C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783404 | |||||||
chr4:89783443 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+38803T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783443 | |||||||
chr4:89783466 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+38780C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783466 | |||||||
chr4:89783491 | T | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+38755A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783491 | |||||||
chr4:89783666 | G | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+38580C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783666 | |||||||
chr4:89783725 | C | T | 142 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(139): Show |
151 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.306+38521G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783725 | |||||||
chr4:89783752 | A | G | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+38494T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783752 | |||||||
chr4:89783776 | A | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0165 others(1): Show |
5 | NA18947.hp1 NA18951.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+38470T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783776 | |||||||
chr4:89783995 | T | G | 2 | a0001c0001t0003g0119 a0001c0001t0003g0120 |
2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.306+38251A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89783995 | |||||||
chr4:89784053 | C | T | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+38193G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784053 | |||||||
chr4:89784213 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(262): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.306+38033T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784213 | |||||||
chr4:89784277 | G | T | 1 | a0001c0001t0002g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.306+37969C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784277 | |||||||
chr4:89784360 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0027 |
4 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+37886A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784360 | |||||||
chr4:89784429 | A | G | 2 | a0001c0001t0014g0316 a0001c0001t0014g0317 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.306+37817T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784429 | |||||||
chr4:89784455 | T | C | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.306+37791A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784455 | |||||||
chr4:89784610 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0165 others(1): Show |
5 | NA18947.hp1 NA18951.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+37636G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784610 | |||||||
chr4:89784792 | G | A | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+37454C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784792 | |||||||
chr4:89784842 | GTGGGAAG others(32): Show |
G | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37365_306+3740 others(43): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784842 | |||||||
chr4:89784882 | T | G | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37364A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784882 | |||||||
chr4:89784884 | G | T | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37362C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784884 | |||||||
chr4:89784887 | C | A | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37359G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784887 | |||||||
chr4:89784889 | C | A | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37357G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784889 | |||||||
chr4:89784890 | A | T | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37356T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784890 | |||||||
chr4:89784891 | C | T | 1 | a0001c0001t0011g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+37355G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89784891 | |||||||
chr4:89785235 | A | G | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+37011T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89785235 | |||||||
chr4:89785345 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.306+36901G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89785345 | |||||||
chr4:89785439 | A | T | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+36807T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89785439 | |||||||
chr4:89785615 | G | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+36631C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89785615 | |||||||
chr4:89785845 | G | A | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+36401C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89785845 | |||||||
chr4:89786252 | A | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+35994T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786252 | |||||||
chr4:89786313 | C | A | 11 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+35933G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786313 | |||||||
chr4:89786459 | A | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+35787T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786459 | |||||||
chr4:89786480 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18945.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.306+35766A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786480 | |||||||
chr4:89786559 | G | GCTTAATA others(6): Show |
1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+35674_306+3568 others(17): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786559 | |||||||
chr4:89786560 | C | A | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+35686G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786560 | |||||||
chr4:89786620 | C | CA | 14 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 others(11): Show |
14 | HG00741.hp2 HG01258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+35625dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786620 | |||||||
chr4:89786620 | C | CAA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(156): Show |
165 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.306+35624_306+3562 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786620 | |||||||
chr4:89786620 | C | CAAA | 37 | a0001c0001t0001g0299 a0001c0001t0002g0013 a0001c0001t0002g0235 others(34): Show |
40 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+35623_306+3562 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786620 | |||||||
chr4:89786620 | C | CAAAA | 53 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(50): Show |
58 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.306+35622_306+3562 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786620 | |||||||
chr4:89786620 | CA | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
8 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+35625delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786620 | |||||||
chr4:89786752 | C | T | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+35494G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786752 | |||||||
chr4:89786796 | T | C | 34 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(31): Show |
36 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.306+35450A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786796 | |||||||
chr4:89786959 | A | G | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+35287T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89786959 | |||||||
chr4:89787030 | T | C | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0007g0304 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.306+35216A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787030 | |||||||
chr4:89787032 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.306+35214C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787032 | |||||||
chr4:89787067 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.306+35179A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787067 | |||||||
chr4:89787348 | T | C | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+34898A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787348 | |||||||
chr4:89787356 | C | T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0027 others(7): Show |
12 | HG01109.hp1 HG01978.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.306+34890G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787356 | |||||||
chr4:89787715 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+34531C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787715 | |||||||
chr4:89787776 | C | CA | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+34469dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787776 | |||||||
chr4:89787809 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+34437C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787809 | |||||||
chr4:89787937 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.306+34309A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89787937 | |||||||
chr4:89788018 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(294): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.306+34228C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788018 | |||||||
chr4:89788019 | T | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+34227A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788019 | |||||||
chr4:89788071 | C | CGT | 83 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(80): Show |
87 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.306+34173_306+3417 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788071 | |||||||
chr4:89788079 | TGA | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(109): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.306+34165_306+3416 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788079 | |||||||
chr4:89788081 | A | T | 142 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(139): Show |
151 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.306+34165T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788081 | |||||||
chr4:89788081 | AGAGT | A | 5 | a0001c0001t0001g0189 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+34161_306+3416 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788081 | |||||||
chr4:89788083 | A | AGT | 53 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0077 others(50): Show |
56 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.306+34161_306+3416 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788083 | |||||||
chr4:89788083 | A | T | 61 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0243 others(58): Show |
66 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.306+34163T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788083 | |||||||
chr4:89788085 | T | A | 59 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(56): Show |
64 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.306+34161A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788085 | |||||||
chr4:89788134 | A | G | 2 | a0001c0001t0002g0236 a0001c0001t0002g0262 |
2 | HG00408.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.306+34112T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788134 | |||||||
chr4:89788339 | T | C | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+33907A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788339 | |||||||
chr4:89788590 | G | A | 142 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(139): Show |
151 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.306+33656C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788590 | |||||||
chr4:89788851 | C | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+33395G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788851 | |||||||
chr4:89788887 | G | A | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+33359C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788887 | |||||||
chr4:89788948 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+33298G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89788948 | |||||||
chr4:89789098 | CAGAAGA | C | 3 | a0001c0001t0002g0013 a0001c0001t0012g0281 a0001c0001t0034g0319 |
4 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+33142_306+3314 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789098 | |||||||
chr4:89789437 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+32809C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789437 | |||||||
chr4:89789526 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+32720A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789526 | |||||||
chr4:89789578 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.306+32668A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789578 | |||||||
chr4:89789697 | A | C | 1 | a0001c0001t0020g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306+32549T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789697 | |||||||
chr4:89789922 | G | A | 2 | a0001c0001t0002g0258 a0001c0001t0002g0283 |
2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.306+32324C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89789922 | |||||||
chr4:89790085 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.306+32161C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790085 | |||||||
chr4:89790148 | C | T | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+32098G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790148 | |||||||
chr4:89790279 | T | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA18943.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.306+31967A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790279 | |||||||
chr4:89790310 | C | T | 1 | a0001c0001t0004g0311 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.306+31936G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790310 | |||||||
chr4:89790311 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.306+31935C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790311 | |||||||
chr4:89790619 | T | C | 169 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(166): Show |
180 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.306+31627A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89790619 | |||||||
chr4:89791005 | C | CT | 86 | a0001c0001t0001g0040 a0001c0001t0001g0081 a0001c0001t0001g0082 others(83): Show |
90 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.306+31240dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791005 | |||||||
chr4:89791005 | C | CTT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(150): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.306+31239_306+3124 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791005 | |||||||
chr4:89791005 | C | CTTT | 16 | a0001c0001t0001g0139 a0001c0001t0001g0172 a0001c0001t0001g0203 others(13): Show |
18 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.306+31238_306+3124 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791005 | |||||||
chr4:89791029 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+31217T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791029 | |||||||
chr4:89791054 | C | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(262): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.306+31192G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791054 | |||||||
chr4:89791208 | A | G | 11 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+31038T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791208 | |||||||
chr4:89791314 | C | T | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+30932G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791314 | |||||||
chr4:89791360 | G | A | 82 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(79): Show |
85 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.306+30886C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791360 | |||||||
chr4:89791364 | C | CT | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(253): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.306+30881dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791364 | |||||||
chr4:89791390 | T | C | 1 | a0001c0001t0020g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306+30856A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791390 | |||||||
chr4:89791405 | C | CT | 79 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0001g0299 others(76): Show |
86 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.306+30840dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791405 | |||||||
chr4:89791452 | G | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02809.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+30794C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791452 | |||||||
chr4:89791478 | T | C | 82 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(79): Show |
85 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.306+30768A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791478 | |||||||
chr4:89791533 | G | GA | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+30712dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791533 | |||||||
chr4:89791913 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.306+30333C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89791913 | |||||||
chr4:89792073 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.306+30173A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792073 | |||||||
chr4:89792108 | G | A | 62 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.306+30138C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792108 | |||||||
chr4:89792109 | C | A | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+30137G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792109 | |||||||
chr4:89792179 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+30067G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792179 | |||||||
chr4:89792279 | G | T | 1 | a0001c0001t0002g0271 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.306+29967C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792279 | |||||||
chr4:89792290 | T | A | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.306+29956A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792290 | |||||||
chr4:89792291 | TTTG | T | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0082 others(57): Show |
64 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.306+29952_306+2995 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTG | T | 43 | a0001c0001t0001g0040 a0001c0001t0001g0090 a0001c0001t0001g0109 others(40): Show |
44 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.306+29949_306+2995 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTGT others(2): Show |
T | 16 | a0001c0001t0001g0081 a0001c0001t0001g0126 a0001c0001t0001g0139 others(13): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.306+29946_306+2995 others(13): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTGT others(5): Show |
T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(110): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.306+29943_306+2995 others(16): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTGT others(8): Show |
T | 1 | a0001c0001t0018g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.306+29940_306+2995 others(19): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTGT others(14): Show |
T | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+29934_306+2995 others(25): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792291 | TTTGTTGT others(17): Show |
T | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+29931_306+2995 others(28): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792291 | |||||||
chr4:89792417 | T | C | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+29829A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792417 | |||||||
chr4:89792470 | G | A | 1 | a0001c0001t0015g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.306+29776C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792470 | |||||||
chr4:89792471 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.306+29775G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792471 | |||||||
chr4:89792523 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+29723T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792523 | |||||||
chr4:89792555 | T | A | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+29691A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792555 | |||||||
chr4:89792573 | A | T | 1 | a0001c0001t0035g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.306+29673T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792573 | |||||||
chr4:89792596 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+29650A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792596 | |||||||
chr4:89792614 | C | T | 8 | a0001c0001t0006g0032 a0001c0001t0006g0033 a0001c0001t0006g0034 others(5): Show |
8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+29632G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792614 | |||||||
chr4:89792944 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+29302C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89792944 | |||||||
chr4:89793080 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+29166G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793080 | |||||||
chr4:89793484 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+28762T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793484 | |||||||
chr4:89793742 | A | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+28504T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793742 | |||||||
chr4:89793867 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.306+28379G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793867 | |||||||
chr4:89793881 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.306+28365T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793881 | |||||||
chr4:89793936 | C | A | 1 | a0001c0001t0002g0045 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.306+28310G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793936 | |||||||
chr4:89793966 | C | G | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+28280G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793966 | |||||||
chr4:89793972 | TACTC | T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+28270_306+2827 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89793972 | |||||||
chr4:89794077 | A | G | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+28169T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794077 | |||||||
chr4:89794080 | C | T | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+28166G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794080 | |||||||
chr4:89794150 | T | C | 4 | a0001c0001t0006g0034 a0001c0001t0006g0037 a0001c0001t0006g0038 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+28096A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794150 | |||||||
chr4:89794221 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.306+28025T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794221 | |||||||
chr4:89794291 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.306+27955A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794291 | |||||||
chr4:89794340 | C | T | 2 | a0001c0001t0004g0308 a0001c0002t0004g0307 |
2 | HG00733.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.306+27906G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794340 | |||||||
chr4:89794523 | T | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+27723A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794523 | |||||||
chr4:89794654 | T | C | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+27592A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794654 | |||||||
chr4:89794709 | T | TA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+27536dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794709 | |||||||
chr4:89794775 | T | C | 1 | a0001c0001t0007g0143 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.306+27471A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794775 | |||||||
chr4:89794857 | A | G | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+27389T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794857 | |||||||
chr4:89794955 | T | C | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.306+27291A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794955 | |||||||
chr4:89794988 | C | G | 63 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(60): Show |
66 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.306+27258G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89794988 | |||||||
chr4:89795026 | C | G | 14 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(11): Show |
14 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+27220G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795026 | |||||||
chr4:89795239 | A | G | 10 | a0001c0001t0001g0243 a0001c0001t0002g0002 a0001c0001t0002g0003 others(7): Show |
14 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.306+27007T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795239 | |||||||
chr4:89795291 | G | C | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+26955C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795291 | |||||||
chr4:89795347 | A | AT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0176 a0001c0001t0001g0243 others(6): Show |
9 | HG03017.hp2 HG03195.hp2 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+26898dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795347 | |||||||
chr4:89795347 | A | ATTTT | 54 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0026 others(51): Show |
57 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.306+26895_306+2689 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795347 | |||||||
chr4:89795347 | A | ATTTTT | 7 | a0001c0001t0001g0040 a0001c0001t0002g0030 a0001c0001t0002g0047 others(4): Show |
7 | HG02027.hp1 HG02559.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+26894_306+2689 others(9): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795347 | |||||||
chr4:89795347 | AT | A | 17 | a0001c0001t0001g0171 a0001c0001t0001g0192 a0001c0001t0001g0193 others(14): Show |
18 | HG01109.hp2 HG01169.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.306+26898delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795347 | |||||||
chr4:89795701 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+26545A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795701 | |||||||
chr4:89795794 | C | A | 2 | a0001c0001t0002g0238 a0001c0001t0002g0240 |
2 | NA18984.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.306+26452G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795794 | |||||||
chr4:89795796 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.306+26450T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795796 | |||||||
chr4:89795801 | C | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+26445G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795801 | |||||||
chr4:89795865 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+26381T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89795865 | |||||||
chr4:89796027 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.306+26219G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796027 | |||||||
chr4:89796094 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+26152C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796094 | |||||||
chr4:89796096 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.306+26150C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796096 | |||||||
chr4:89796274 | CA | C | 74 | a0001c0001t0001g0091 a0001c0001t0001g0243 a0001c0001t0001g0251 others(71): Show |
79 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.306+25971delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796274 | |||||||
chr4:89796274 | CAA | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(110): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.306+25970_306+2597 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796274 | |||||||
chr4:89796282 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.306+25964T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796282 | |||||||
chr4:89796284 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+25962T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796284 | |||||||
chr4:89796284 | AAT | A | 17 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(14): Show |
17 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.306+25960_306+2596 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796284 | |||||||
chr4:89796285 | AT | A | 56 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(53): Show |
59 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.306+25960delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796285 | |||||||
chr4:89796286 | T | A | 9 | a0001c0001t0001g0115 a0001c0001t0002g0036 a0001c0001t0003g0096 others(6): Show |
10 | HG00609.hp2 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+25960A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796286 | |||||||
chr4:89796288 | T | A | 5 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0011g0282 others(2): Show |
5 | HG03139.hp2 HG03195.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+25958A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796288 | |||||||
chr4:89796336 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+25910A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796336 | |||||||
chr4:89796584 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.306+25662G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796584 | |||||||
chr4:89796904 | T | A | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+25342A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796904 | |||||||
chr4:89796939 | A | G | 3 | a0001c0001t0015g0129 a0001c0001t0015g0130 a0001c0001t0020g0131 |
3 | HG01891.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+25307T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796939 | |||||||
chr4:89796982 | C | T | 2 | a0001c0001t0002g0271 a0001c0001t0017g0244 |
2 | HG02004.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.306+25264G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89796982 | |||||||
chr4:89797239 | G | C | 2 | a0001c0001t0004g0293 a0001c0001t0004g0306 |
2 | HG01261.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.306+25007C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797239 | |||||||
chr4:89797387 | C | T | 1 | a0001c0001t0014g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.306+24859G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797387 | |||||||
chr4:89797568 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+24678G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797568 | |||||||
chr4:89797670 | T | C | 3 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.306+24576A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797670 | |||||||
chr4:89797783 | C | A | 1 | a0001c0001t0002g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.306+24463G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797783 | |||||||
chr4:89797844 | C | T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG00639.hp1 HG01071.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+24402G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797844 | |||||||
chr4:89797869 | G | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+24377C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89797869 | |||||||
chr4:89798041 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+24205T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798041 | |||||||
chr4:89798045 | A | T | 76 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(73): Show |
81 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.306+24201T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798045 | |||||||
chr4:89798114 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.306+24132C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798114 | |||||||
chr4:89798173 | C | CA | 7 | a0001c0001t0002g0030 a0001c0001t0002g0042 a0001c0001t0002g0061 others(4): Show |
7 | HG00597.hp2 HG02027.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+24072dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798173 | |||||||
chr4:89798180 | A | AG | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+24065_306+2406 others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798180 | |||||||
chr4:89798309 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+23937A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798309 | |||||||
chr4:89798348 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.306+23898C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798348 | |||||||
chr4:89798359 | C | G | 1 | a0001c0001t0002g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306+23887G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798359 | |||||||
chr4:89798737 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0074 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.306+23509A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798737 | |||||||
chr4:89798781 | G | A | 1 | a0001c0001t0012g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.306+23465C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798781 | |||||||
chr4:89798788 | G | A | 3 | a0001c0001t0002g0036 a0001c0001t0016g0277 a0001c0001t0016g0278 |
3 | HG01243.hp1 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.306+23458C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798788 | |||||||
chr4:89798887 | T | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 |
3 | HG00741.hp2 HG01258.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.306+23359A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798887 | |||||||
chr4:89798984 | T | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0008g0218 |
3 | NA18949.hp1 NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.306+23262A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89798984 | |||||||
chr4:89799083 | G | A | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+23163C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799083 | |||||||
chr4:89799214 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+23032A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799214 | |||||||
chr4:89799564 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.306+22682A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799564 | |||||||
chr4:89799588 | C | T | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+22658G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799588 | |||||||
chr4:89799693 | T | C | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.306+22553A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799693 | |||||||
chr4:89799806 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+22440T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89799806 | |||||||
chr4:89800020 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.306+22226C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800020 | |||||||
chr4:89800341 | G | A | 11 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+21905C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800341 | |||||||
chr4:89800409 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+21837T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800409 | |||||||
chr4:89800486 | C | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+21760G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800486 | |||||||
chr4:89800499 | C | T | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+21747G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800499 | |||||||
chr4:89800729 | T | C | 77 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(74): Show |
82 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.306+21517A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800729 | |||||||
chr4:89800735 | G | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+21511C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800735 | |||||||
chr4:89800744 | A | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+21502T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800744 | |||||||
chr4:89800808 | A | C | 1 | a0001c0001t0006g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+21438T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800808 | |||||||
chr4:89800846 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+21400C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800846 | |||||||
chr4:89800994 | A | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+21252T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89800994 | |||||||
chr4:89801168 | T | C | 4 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+21078A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801168 | |||||||
chr4:89801249 | C | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+20997G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801249 | |||||||
chr4:89801282 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+20964C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801282 | |||||||
chr4:89801494 | C | T | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+20752G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801494 | |||||||
chr4:89801532 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+20714A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801532 | |||||||
chr4:89801681 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+20565T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801681 | |||||||
chr4:89801720 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+20526G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801720 | |||||||
chr4:89801866 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.306+20380G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89801866 | |||||||
chr4:89802187 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.306+20059T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802187 | |||||||
chr4:89802424 | CT | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(214): Show |
229 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.306+19821delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802424 | |||||||
chr4:89802424 | CTT | C | 6 | a0001c0001t0001g0158 a0001c0001t0001g0199 a0001c0001t0002g0031 others(3): Show |
6 | HG03209.hp1 HG03654.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+19820_306+1982 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802424 | |||||||
chr4:89802425 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.306+19821A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802425 | |||||||
chr4:89802548 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.306+19698G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802548 | |||||||
chr4:89802581 | ATCTG | A | 20 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(17): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.306+19661_306+1966 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802581 | |||||||
chr4:89802585 | G | T | 2 | a0001c0001t0004g0308 a0001c0002t0004g0307 |
2 | HG00733.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.306+19661C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802585 | |||||||
chr4:89802592 | T | TTTTCTTT others(13): Show |
4 | a0001c0001t0002g0035 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG03486.hp1 NA18949.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+19634_306+1965 others(24): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(17): Show |
3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0033g0049 |
3 | HG03490.hp1 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.306+19630_306+1965 others(28): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(21): Show |
8 | a0001c0001t0002g0031 a0001c0001t0002g0041 a0001c0001t0002g0050 others(5): Show |
8 | HG02602.hp1 HG03654.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+19653_306+1965 others(32): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(25): Show |
19 | a0001c0001t0002g0006 a0001c0001t0002g0026 a0001c0001t0002g0030 others(16): Show |
21 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.306+19653_306+1965 others(36): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(29): Show |
15 | a0001c0001t0002g0005 a0001c0001t0002g0027 a0001c0001t0002g0036 others(12): Show |
16 | HG01109.hp1 HG01167.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.306+19653_306+1965 others(40): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(33): Show |
10 | a0001c0001t0002g0044 a0001c0001t0002g0067 a0001c0001t0002g0073 others(7): Show |
10 | HG00673.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+19653_306+1965 others(44): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | T | TTTTCTTT others(37): Show |
6 | a0001c0001t0001g0040 a0001c0001t0002g0028 a0001c0001t0002g0045 others(3): Show |
6 | HG02615.hp1 HG04228.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+19653_306+1965 others(48): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | TTTTC | T | 6 | a0001c0001t0001g0172 a0001c0001t0009g0017 a0001c0001t0009g0018 others(3): Show |
6 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+19650_306+1965 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802592 | TTTTCTTT others(5): Show |
T | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+19642_306+1965 others(16): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802592 | |||||||
chr4:89802614 | TTCTTTTT others(1): Show |
T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.306+19624_306+1963 others(12): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802614 | |||||||
chr4:89802616 | C | CTTTCTTT others(26): Show |
1 | a0001c0001t0006g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.306+19629_306+1963 others(37): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802616 | |||||||
chr4:89802618 | T | TTCTTTCT others(31): Show |
1 | a0001c0001t0002g0072 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.306+19627_306+1962 others(42): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802618 | |||||||
chr4:89802619 | T | TCTTTCTT others(30): Show |
1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.306+19626_306+1962 others(41): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802619 | |||||||
chr4:89802636 | C | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.306+19610G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802636 | |||||||
chr4:89802705 | T | C | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+19541A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802705 | |||||||
chr4:89802715 | CTTTT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(189): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.306+19527_306+1953 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802715 | |||||||
chr4:89802717 | T | A | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+19529A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802717 | |||||||
chr4:89802719 | T | C | 1 | a0001c0001t0002g0257 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.306+19527A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802719 | |||||||
chr4:89802729 | GTTCTTTC others(6): Show |
G | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.306+19504_306+1951 others(17): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802729 | |||||||
chr4:89802741 | TTTTCTTT others(5): Show |
T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0026 others(58): Show |
64 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.306+19493_306+1950 others(16): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802741 | |||||||
chr4:89802810 | G | A | 2 | a0001c0001t0004g0015 a0001c0001t0007g0312 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.306+19436C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802810 | |||||||
chr4:89802890 | T | A | 3 | a0001c0001t0016g0277 a0001c0001t0016g0278 a0001c0001t0026g0289 |
3 | HG01243.hp1 HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.306+19356A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802890 | |||||||
chr4:89802961 | C | A | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.306+19285G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89802961 | |||||||
chr4:89803006 | T | A | 1 | a0001c0001t0002g0257 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.306+19240A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803006 | |||||||
chr4:89803079 | T | C | 1 | a0001c0001t0024g0315 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.306+19167A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803079 | |||||||
chr4:89803127 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.306+19119C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803127 | |||||||
chr4:89803222 | T | A | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+19024A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803222 | |||||||
chr4:89803273 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.306+18973A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803273 | |||||||
chr4:89803300 | T | C | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.306+18946A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803300 | |||||||
chr4:89803372 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.306+18874G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803372 | |||||||
chr4:89803404 | T | C | 5 | a0001c0001t0005g0004 a0001c0001t0005g0022 a0001c0001t0005g0023 others(2): Show |
6 | HG01109.hp1 HG01978.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+18842A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803404 | |||||||
chr4:89803521 | T | C | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+18725A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803521 | |||||||
chr4:89803598 | G | T | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.306+18648C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803598 | |||||||
chr4:89803640 | T | A | 1 | a0001c0001t0024g0315 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.306+18606A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803640 | |||||||
chr4:89803642 | C | T | 1 | a0001c0001t0028g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.306+18604G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803642 | |||||||
chr4:89803650 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.306+18596A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803650 | |||||||
chr4:89803718 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+18528C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803718 | |||||||
chr4:89803733 | C | T | 1 | a0001c0001t0012g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.306+18513G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803733 | |||||||
chr4:89803835 | T | C | 3 | a0001c0001t0015g0129 a0001c0001t0015g0130 a0001c0001t0020g0131 |
3 | HG01891.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+18411A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803835 | |||||||
chr4:89803904 | T | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+18342A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89803904 | |||||||
chr4:89804218 | G | A | 10 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 others(7): Show |
10 | HG00609.hp2 NA18941.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+18028C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804218 | |||||||
chr4:89804383 | G | A | 1 | a0001c0001t0014g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.306+17863C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804383 | |||||||
chr4:89804385 | T | C | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+17861A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804385 | |||||||
chr4:89804387 | T | G | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+17859A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804387 | |||||||
chr4:89804446 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.306+17800A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804446 | |||||||
chr4:89804463 | T | C | 2 | a0001c0001t0011g0010 a0001c0001t0027g0101 |
3 | HG03139.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.306+17783A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804463 | |||||||
chr4:89804471 | A | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0042 a0001c0001t0002g0043 others(3): Show |
6 | NA18967.hp2 NA18990.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+17775T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804471 | |||||||
chr4:89804598 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+17648T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804598 | |||||||
chr4:89804812 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.306+17434T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804812 | |||||||
chr4:89804871 | T | G | 77 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(74): Show |
82 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.306+17375A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804871 | |||||||
chr4:89804938 | C | A | 77 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(74): Show |
82 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.306+17308G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804938 | |||||||
chr4:89804949 | T | C | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+17297A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89804949 | |||||||
chr4:89805101 | T | C | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+17145A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805101 | |||||||
chr4:89805215 | C | CTTTGCAT others(35): Show |
1 | a0001c0001t0002g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.306+16989_306+1703 others(46): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805215 | |||||||
chr4:89805353 | C | CA | 68 | a0001c0001t0001g0085 a0001c0001t0001g0194 a0001c0001t0001g0222 others(65): Show |
73 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.306+16892dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805353 | |||||||
chr4:89805353 | C | CAAA | 21 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(18): Show |
23 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.306+16890_306+1689 others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805353 | |||||||
chr4:89805363 | A | AC | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+16882_306+1688 others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805363 | |||||||
chr4:89805381 | C | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.306+16865G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805381 | |||||||
chr4:89805385 | C | T | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+16861G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805385 | |||||||
chr4:89805471 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.306+16775C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805471 | |||||||
chr4:89805476 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+16770T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805476 | |||||||
chr4:89805605 | A | T | 2 | a0001c0001t0007g0142 a0001c0001t0007g0143 |
2 | HG01167.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.306+16641T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805605 | |||||||
chr4:89805706 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.306+16540T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805706 | |||||||
chr4:89805748 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+16498T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805748 | |||||||
chr4:89805810 | AT | A | 14 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(11): Show |
14 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+16435delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805810 | |||||||
chr4:89805813 | T | A | 14 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(11): Show |
14 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+16433A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805813 | |||||||
chr4:89805937 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+16309G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89805937 | |||||||
chr4:89806036 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.306+16210C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806036 | |||||||
chr4:89806063 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.306+16183G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806063 | |||||||
chr4:89806064 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+16182C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806064 | |||||||
chr4:89806067 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+16179T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806067 | |||||||
chr4:89806164 | T | C | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+16082A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806164 | |||||||
chr4:89806337 | T | C | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+15909A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806337 | |||||||
chr4:89806433 | T | A | 1 | a0001c0001t0002g0068 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.306+15813A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806433 | |||||||
chr4:89806541 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0115 |
3 | HG03130.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.306+15705C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806541 | |||||||
chr4:89806772 | G | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+15474C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806772 | |||||||
chr4:89806948 | T | G | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+15298A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89806948 | |||||||
chr4:89807030 | A | C | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+15216T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807030 | |||||||
chr4:89807172 | T | TG | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+15073dupC | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807172 | |||||||
chr4:89807272 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+14974C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807272 | |||||||
chr4:89807528 | TAAAG | T | 7 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+14714_306+1471 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807528 | |||||||
chr4:89807583 | C | A | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.306+14663G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807583 | |||||||
chr4:89807671 | C | T | 1 | a0001c0001t0006g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+14575G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807671 | |||||||
chr4:89807693 | T | C | 1 | a0001c0001t0035g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.306+14553A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807693 | |||||||
chr4:89807697 | C | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.306+14549G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89807697 | |||||||
chr4:89808184 | T | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.306+14062A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808184 | |||||||
chr4:89808211 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.306+14035C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808211 | |||||||
chr4:89808451 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+13795T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808451 | |||||||
chr4:89808515 | G | T | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.306+13731C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808515 | |||||||
chr4:89808596 | T | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+13650A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808596 | |||||||
chr4:89808997 | C | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+13249G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89808997 | |||||||
chr4:89809435 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.306+12811C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809435 | |||||||
chr4:89809495 | T | TAC | 67 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0083 others(64): Show |
69 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.306+12749_306+1275 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | T | TACAC | 59 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0147 others(56): Show |
64 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.306+12747_306+1275 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | T | TACACAC | 10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
10 | HG02074.hp2 HG02155.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+12745_306+1275 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | TAC | T | 79 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(76): Show |
83 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.306+12749_306+1275 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | TACAC | T | 19 | a0001c0001t0001g0099 a0001c0001t0002g0013 a0001c0001t0002g0080 others(16): Show |
20 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.306+12747_306+1275 others(8): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | TACACAC | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0022 a0001c0001t0005g0023 others(7): Show |
11 | HG01109.hp1 HG01167.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+12745_306+1275 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809495 | TACACACA others(9): Show |
T | 3 | a0001c0001t0015g0129 a0001c0001t0015g0130 a0001c0001t0020g0131 |
3 | HG01891.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+12735_306+1275 others(20): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809495 | |||||||
chr4:89809530 | A | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+12716T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809530 | |||||||
chr4:89809536 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(89): Show |
95 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.306+12710G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89809536 | |||||||
chr4:89810255 | A | G | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+11991T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810255 | |||||||
chr4:89810307 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.306+11939C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810307 | |||||||
chr4:89810338 | G | A | 1 | a0001c0001t0009g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.306+11908C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810338 | |||||||
chr4:89810534 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+11712C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810534 | |||||||
chr4:89810558 | A | G | 14 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(11): Show |
14 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+11688T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810558 | |||||||
chr4:89810585 | C | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+11661G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810585 | |||||||
chr4:89810845 | A | G | 11 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.306+11401T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810845 | |||||||
chr4:89810991 | A | C | 1 | a0001c0001t0002g0238 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.306+11255T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89810991 | |||||||
chr4:89811222 | ATATCAC | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(91): Show |
98 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.306+11018_306+1102 others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811222 | |||||||
chr4:89811355 | C | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+10891G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811355 | |||||||
chr4:89811407 | C | T | 1 | a0001c0001t0006g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+10839G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811407 | |||||||
chr4:89811464 | C | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+10782G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811464 | |||||||
chr4:89811652 | A | T | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+10594T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811652 | |||||||
chr4:89811712 | C | A | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+10534G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811712 | |||||||
chr4:89811968 | TGA | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+10276_306+1027 others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89811968 | |||||||
chr4:89812078 | G | A | 1 | a0001c0001t0003g0116 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.306+10168C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812078 | |||||||
chr4:89812228 | G | T | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+10018C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812228 | |||||||
chr4:89812518 | A | G | 2 | a0001c0001t0004g0015 a0001c0001t0007g0312 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.306+9728T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812518 | |||||||
chr4:89812522 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.306+9724G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812522 | |||||||
chr4:89812685 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+9561A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812685 | |||||||
chr4:89812807 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.306+9439C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812807 | |||||||
chr4:89812906 | G | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+9340C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812906 | |||||||
chr4:89812954 | C | G | 67 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(64): Show |
70 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.306+9292G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812954 | |||||||
chr4:89812960 | G | T | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+9286C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89812960 | |||||||
chr4:89813178 | A | G | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+9068T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813178 | |||||||
chr4:89813182 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+9064A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813182 | |||||||
chr4:89813265 | C | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+8981G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813265 | |||||||
chr4:89813275 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+8971A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813275 | |||||||
chr4:89813384 | T | G | 77 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(74): Show |
82 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.306+8862A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813384 | |||||||
chr4:89813482 | C | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+8764G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813482 | |||||||
chr4:89813503 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.306+8743G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813503 | |||||||
chr4:89813577 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+8669T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813577 | |||||||
chr4:89813725 | G | C | 1 | a0001c0001t0002g0260 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.306+8521C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813725 | |||||||
chr4:89813763 | C | A | 57 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.306+8483G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813763 | |||||||
chr4:89813810 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+8436C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89813810 | |||||||
chr4:89814051 | C | T | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+8195G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814051 | |||||||
chr4:89814855 | A | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+7391T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814855 | |||||||
chr4:89814856 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | NA18943.hp1 NA18978.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.306+7390C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814856 | |||||||
chr4:89814873 | A | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+7373T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814873 | |||||||
chr4:89814922 | A | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18945.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.306+7324T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814922 | |||||||
chr4:89814962 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+7284A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814962 | |||||||
chr4:89814971 | C | A | 63 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(60): Show |
68 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.306+7275G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814971 | |||||||
chr4:89814980 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+7266G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814980 | |||||||
chr4:89814985 | A | G | 1 | a0002c0003t0002g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.306+7261T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89814985 | |||||||
chr4:89815119 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.306+7127C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815119 | |||||||
chr4:89815268 | A | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0013g0212 |
3 | HG02559.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.306+6978T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815268 | |||||||
chr4:89815366 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(89): Show |
95 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.306+6880A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815366 | |||||||
chr4:89815434 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+6812G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815434 | |||||||
chr4:89815527 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+6719T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815527 | |||||||
chr4:89815547 | G | A | 16 | a0001c0001t0002g0012 a0001c0001t0002g0226 a0001c0001t0002g0228 others(13): Show |
17 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.306+6699C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815547 | |||||||
chr4:89815576 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+6670T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815576 | |||||||
chr4:89815635 | A | C | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+6611T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815635 | |||||||
chr4:89815767 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.306+6479A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815767 | |||||||
chr4:89815772 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+6474C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815772 | |||||||
chr4:89815951 | C | A | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+6295G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89815951 | |||||||
chr4:89816070 | T | C | 1 | a0001c0001t0005g0270 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.306+6176A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816070 | |||||||
chr4:89816176 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(168): Show |
180 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.306+6070C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816176 | |||||||
chr4:89816329 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0012g0281 |
3 | HG02451.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.306+5917G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816329 | |||||||
chr4:89816333 | A | G | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+5913T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816333 | |||||||
chr4:89816337 | TGATGG | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.306+5904_306+5908d others(7): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816337 | |||||||
chr4:89816393 | T | TTA | 4 | a0001c0001t0002g0002 a0001c0001t0002g0271 a0001c0001t0002g0272 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+5851_306+5852d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816393 | |||||||
chr4:89816420 | T | C | 1 | a0002c0003t0002g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.306+5826A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816420 | |||||||
chr4:89816482 | A | G | 1 | a0001c0001t0005g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.306+5764T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816482 | |||||||
chr4:89816728 | G | C | 76 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(73): Show |
81 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.306+5518C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816728 | |||||||
chr4:89816919 | T | C | 1 | a0001c0001t0004g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.306+5327A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816919 | |||||||
chr4:89816997 | T | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+5249A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89816997 | |||||||
chr4:89817007 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.306+5239C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817007 | |||||||
chr4:89817041 | CT | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+5204delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817041 | |||||||
chr4:89817411 | T | A | 1 | a0001c0001t0006g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.306+4835A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817411 | |||||||
chr4:89817521 | C | T | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+4725G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817521 | |||||||
chr4:89817643 | G | A | 3 | a0001c0001t0015g0129 a0001c0001t0015g0130 a0001c0001t0020g0131 |
3 | HG01891.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.306+4603C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817643 | |||||||
chr4:89817688 | T | G | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+4558A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817688 | |||||||
chr4:89817933 | A | C | 5 | a0001c0001t0007g0134 a0001c0001t0007g0142 a0001c0001t0007g0143 others(2): Show |
5 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+4313T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89817933 | |||||||
chr4:89818097 | T | C | 62 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.306+4149A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818097 | |||||||
chr4:89818104 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+4142T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818104 | |||||||
chr4:89818132 | CT | C | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+4113delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818132 | |||||||
chr4:89818223 | T | C | 3 | a0001c0001t0011g0010 a0001c0001t0011g0118 a0001c0001t0027g0101 |
4 | HG03139.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+4023A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818223 | |||||||
chr4:89818337 | C | T | 6 | a0001c0001t0003g0103 a0001c0001t0003g0104 a0001c0001t0003g0105 others(3): Show |
6 | NA18955.hp2 NA18978.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+3909G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818337 | |||||||
chr4:89818354 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+3892A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818354 | |||||||
chr4:89818388 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(168): Show |
180 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.306+3858G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818388 | |||||||
chr4:89818511 | A | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+3735T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818511 | |||||||
chr4:89818710 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.306+3536A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818710 | |||||||
chr4:89818841 | T | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+3405A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818841 | |||||||
chr4:89818952 | G | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+3294C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89818952 | |||||||
chr4:89819653 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.306+2593T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89819653 | |||||||
chr4:89819726 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.306+2520G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89819726 | |||||||
chr4:89819727 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(190): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.306+2519C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89819727 | |||||||
chr4:89819731 | G | C | 1 | a0001c0001t0004g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.306+2515C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89819731 | |||||||
chr4:89820356 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.306+1890C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89820356 | |||||||
chr4:89820368 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+1878C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89820368 | |||||||
chr4:89820622 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.306+1624T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89820622 | |||||||
chr4:89820652 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(65): Show |
71 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.306+1594T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89820652 | |||||||
chr4:89820680 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.306+1566A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89820680 | |||||||
chr4:89821033 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.306+1213A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821033 | |||||||
chr4:89821050 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.306+1196G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821050 | |||||||
chr4:89821145 | G | A | 1 | a0001c0001t0008g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.306+1101C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821145 | |||||||
chr4:89821258 | G | C | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.306+988C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821258 | |||||||
chr4:89821260 | AAGGGAGG others(17): Show |
A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.306+962_306+985del others(24): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821260 | |||||||
chr4:89821272 | A | G | 1 | a0001c0001t0013g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.306+974T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821272 | |||||||
chr4:89821279 | G | A | 1 | a0001c0001t0013g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.306+967C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821279 | |||||||
chr4:89821280 | G | GAGGGAGG others(66): Show |
1 | a0001c0001t0013g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.306+965_306+966ins others(73): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821280 | |||||||
chr4:89821284 | G | A | 1 | a0001c0001t0013g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.306+962C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821284 | |||||||
chr4:89821288 | G | GAGGAAGG others(13): Show |
1 | a0001c0001t0003g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.306+938_306+957dup others(20): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821288 | |||||||
chr4:89821291 | G | A | 2 | a0001c0001t0013g0140 a0001c0001t0034g0319 |
2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.306+955C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821291 | |||||||
chr4:89821291 | G | GAAGGAAG others(70): Show |
27 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(24): Show |
29 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.306+954_306+955ins others(77): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821291 | |||||||
chr4:89821300 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+946T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821300 | |||||||
chr4:89821301 | AG | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+944delC | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821301 | |||||||
chr4:89821303 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+943C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821303 | |||||||
chr4:89821304 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+942C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821304 | |||||||
chr4:89821306 | G | A | 29 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(26): Show |
31 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.306+940C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821306 | |||||||
chr4:89821307 | A | G | 29 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(26): Show |
31 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.306+939T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821307 | |||||||
chr4:89821311 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+935C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821311 | |||||||
chr4:89821318 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+928C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821318 | |||||||
chr4:89821321 | AG | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+924delC | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821321 | |||||||
chr4:89821323 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+923C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821323 | |||||||
chr4:89821325 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(151): Show |
160 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.306+921T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821325 | |||||||
chr4:89821333 | G | C | 1 | a0001c0001t0002g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.306+913C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821333 | |||||||
chr4:89821338 | G | GAAAGAAA others(15): Show |
100 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0001g0299 others(97): Show |
108 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.306+907_306+908ins others(22): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821338 | |||||||
chr4:89821338 | G | GAAAGAAA others(15): Show |
6 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0014g0316 others(3): Show |
6 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+907_306+908ins others(22): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821338 | |||||||
chr4:89821458 | C | A | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+788G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821458 | |||||||
chr4:89821488 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(152): Show |
161 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.306+758C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821488 | |||||||
chr4:89821521 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.306+725C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821521 | |||||||
chr4:89821541 | A | G | 71 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(68): Show |
76 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.306+705T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821541 | |||||||
chr4:89821561 | TGTA | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.306+682_306+684del others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821561 | |||||||
chr4:89821593 | G | A | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.306+653C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821593 | |||||||
chr4:89821664 | G | A | 78 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(75): Show |
84 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.306+582C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821664 | |||||||
chr4:89821706 | A | T | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.306+540T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821706 | |||||||
chr4:89821710 | T | G | 78 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(75): Show |
84 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.306+536A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821710 | |||||||
chr4:89821897 | G | C | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306+349C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89821897 | |||||||
chr4:89822013 | A | C | 1 | a0001c0001t0016g0277 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.306+233T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89822013 | |||||||
chr4:89822166 | T | TC | 86 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.306+79dupG | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89822166 | |||||||
chr4:89822180 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(235): Show |
250 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.306+66G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 4/5 | chr4 | 89822180 | |||||||
chr4:89822496 | A | T | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-108T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89822496 | |||||||
chr4:89822540 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.164-152C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89822540 | |||||||
chr4:89822704 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.164-316G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89822704 | |||||||
chr4:89822716 | G | T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-328C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89822716 | |||||||
chr4:89822949 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-561G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89822949 | |||||||
chr4:89823000 | AATT | A | 78 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(75): Show |
84 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.164-615_164-613del others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823000 | |||||||
chr4:89823019 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-631T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823019 | |||||||
chr4:89823065 | G | A | 84 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(81): Show |
90 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-677C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823065 | |||||||
chr4:89823070 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-682G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823070 | |||||||
chr4:89823097 | C | T | 23 | a0001c0001t0001g0162 a0001c0001t0001g0299 a0001c0001t0003g0014 others(20): Show |
25 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.164-709G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823097 | |||||||
chr4:89823119 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-731T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823119 | |||||||
chr4:89823177 | G | A | 62 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.164-789C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823177 | |||||||
chr4:89823197 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.164-809G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823197 | |||||||
chr4:89823204 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.164-816G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823204 | |||||||
chr4:89823435 | A | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.164-1047T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823435 | |||||||
chr4:89823454 | G | A | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.164-1066C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823454 | |||||||
chr4:89823541 | A | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-1153T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823541 | |||||||
chr4:89823564 | G | GAA | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1178_164-1177d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823564 | |||||||
chr4:89823570 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(257): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.164-1182C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823570 | |||||||
chr4:89823654 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0008g0159 a0001c0001t0008g0160 |
3 | HG02698.hp1 HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.164-1266T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823654 | |||||||
chr4:89823752 | G | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1364C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823752 | |||||||
chr4:89823786 | C | CTTATTTA others(1): Show |
14 | a0001c0001t0003g0014 a0001c0001t0004g0015 a0001c0001t0004g0293 others(11): Show |
16 | HG00140.hp1 HG00733.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-1406_164-1399d others(10): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823786 | |||||||
chr4:89823786 | C | CTTATTTA others(5): Show |
8 | a0001c0001t0001g0299 a0001c0001t0004g0302 a0001c0001t0004g0303 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-1410_164-1399d others(14): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823786 | |||||||
chr4:89823786 | C | T | 2 | a0001c0001t0024g0315 a0001c0001t0034g0319 |
2 | HG01243.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.164-1398G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823786 | |||||||
chr4:89823842 | C | CTGGA | 21 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(18): Show |
23 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-1458_164-1455d others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823842 | |||||||
chr4:89823842 | C | T | 152 | a0001c0001t0001g0040 a0001c0001t0001g0243 a0001c0001t0001g0251 others(149): Show |
161 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.164-1454G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823842 | |||||||
chr4:89823878 | C | T | 1 | a0001c0001t0003g0102 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.164-1490G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823878 | |||||||
chr4:89823940 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1552A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823940 | |||||||
chr4:89823945 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(235): Show |
250 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.164-1557C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823945 | |||||||
chr4:89823952 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.164-1564G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823952 | |||||||
chr4:89823953 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1565T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823953 | |||||||
chr4:89823962 | A | C | 71 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(68): Show |
76 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.164-1574T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89823962 | |||||||
chr4:89824087 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1699G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824087 | |||||||
chr4:89824091 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1703A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824091 | |||||||
chr4:89824132 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1744A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824132 | |||||||
chr4:89824194 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.164-1806T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824194 | |||||||
chr4:89824227 | C | G | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-1839G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824227 | |||||||
chr4:89824244 | C | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(257): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.164-1856G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824244 | |||||||
chr4:89824305 | A | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1917T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824305 | |||||||
chr4:89824352 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1964G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824352 | |||||||
chr4:89824416 | T | G | 2 | a0001c0001t0004g0015 a0001c0001t0007g0312 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.164-2028A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824416 | |||||||
chr4:89824556 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-2168C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824556 | |||||||
chr4:89824619 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.164-2231C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824619 | |||||||
chr4:89824662 | A | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164-2274T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824662 | |||||||
chr4:89824779 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(235): Show |
250 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.164-2391G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824779 | |||||||
chr4:89824784 | T | C | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-2396A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824784 | |||||||
chr4:89824845 | T | C | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-2457A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824845 | |||||||
chr4:89824982 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-2594A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89824982 | |||||||
chr4:89825068 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(262): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.164-2680A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825068 | |||||||
chr4:89825170 | C | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-2782G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825170 | |||||||
chr4:89825178 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.164-2790A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825178 | |||||||
chr4:89825185 | G | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.164-2797C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825185 | |||||||
chr4:89825270 | A | G | 1 | a0001c0001t0002g0237 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.163+2873T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825270 | |||||||
chr4:89825315 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(261): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.163+2828C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825315 | |||||||
chr4:89825342 | CATA | C | 78 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(75): Show |
84 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.163+2798_163+2800d others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825342 | |||||||
chr4:89825358 | T | C | 1 | a0001c0001t0008g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.163+2785A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825358 | |||||||
chr4:89825459 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2684C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825459 | |||||||
chr4:89825475 | A | AG | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2667dupC | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825475 | |||||||
chr4:89825495 | G | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.163+2648C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825495 | |||||||
chr4:89825558 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.163+2585G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825558 | |||||||
chr4:89825685 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2458T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825685 | |||||||
chr4:89825727 | G | GA | 234 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(231): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.163+2415dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825727 | |||||||
chr4:89825727 | GA | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2415delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825727 | |||||||
chr4:89825853 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2290T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825853 | |||||||
chr4:89825904 | A | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.163+2239T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89825904 | |||||||
chr4:89826032 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2111C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826032 | |||||||
chr4:89826042 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163+2101T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826042 | |||||||
chr4:89826056 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+2087G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826056 | |||||||
chr4:89826147 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.163+1996G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826147 | |||||||
chr4:89826251 | T | C | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1892A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826251 | |||||||
chr4:89826260 | T | C | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163+1883A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826260 | |||||||
chr4:89826260 | T | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(257): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.163+1883A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826260 | |||||||
chr4:89826348 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1795G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826348 | |||||||
chr4:89826349 | G | A | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163+1794C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826349 | |||||||
chr4:89826354 | A | G | 1 | a0001c0001t0027g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163+1789T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826354 | |||||||
chr4:89826419 | A | G | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.163+1724T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826419 | |||||||
chr4:89826468 | G | GTC | 23 | a0001c0001t0001g0148 a0001c0001t0001g0299 a0001c0001t0003g0014 others(20): Show |
25 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+1673_163+1674d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826468 | |||||||
chr4:89826483 | T | A | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.163+1660A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826483 | |||||||
chr4:89826485 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1658T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826485 | |||||||
chr4:89826487 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1656T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826487 | |||||||
chr4:89826489 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1654T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826489 | |||||||
chr4:89826491 | A | T | 21 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(18): Show |
23 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.163+1652T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826491 | |||||||
chr4:89826493 | G | A | 23 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(20): Show |
25 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+1650C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826493 | |||||||
chr4:89826493 | G | GCA | 9 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(6): Show |
9 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+1648_163+1649d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826493 | |||||||
chr4:89826493 | GCA | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
15 | HG01109.hp2 HG01167.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+1648_163+1649d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826493 | |||||||
chr4:89826520 | C | G | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.163+1623G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826520 | |||||||
chr4:89826522 | C | CACAG | 5 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0006g0037 others(2): Show |
5 | HG02965.hp1 HG03486.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+1620_163+1621i others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826522 | |||||||
chr4:89826522 | C | CAG | 72 | a0001c0001t0001g0136 a0001c0001t0001g0209 a0001c0001t0001g0210 others(69): Show |
77 | HG00438.hp1 HG00621.hp1 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.163+1619_163+1620d others(4): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826522 | |||||||
chr4:89826522 | C | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(158): Show |
168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.163+1621G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826522 | |||||||
chr4:89826553 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1590T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826553 | |||||||
chr4:89826558 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1585G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826558 | |||||||
chr4:89826600 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.163+1543G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826600 | |||||||
chr4:89826698 | C | CT | 3 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0001t0004g0089 |
3 | HG00280.hp1 HG03834.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.163+1444dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826698 | |||||||
chr4:89826732 | G | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(257): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.163+1411C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826732 | |||||||
chr4:89826824 | G | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1319C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826824 | |||||||
chr4:89826902 | C | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163+1241G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89826902 | |||||||
chr4:89827044 | T | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(235): Show |
250 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.163+1099A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827044 | |||||||
chr4:89827133 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+1010G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827133 | |||||||
chr4:89827146 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+997A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827146 | |||||||
chr4:89827223 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.163+920T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827223 | |||||||
chr4:89827259 | G | T | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.163+884C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827259 | |||||||
chr4:89827270 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163+873G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827270 | |||||||
chr4:89827332 | C | G | 1 | a0001c0001t0019g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.163+811G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827332 | |||||||
chr4:89827337 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(262): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.163+806A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827337 | |||||||
chr4:89827495 | C | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+648G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827495 | |||||||
chr4:89827530 | C | A | 6 | a0001c0001t0013g0140 a0001c0001t0013g0141 a0001c0001t0014g0316 others(3): Show |
6 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+613G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827530 | |||||||
chr4:89827559 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.163+584C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827559 | |||||||
chr4:89827587 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+556G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827587 | |||||||
chr4:89827695 | T | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.163+448A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827695 | |||||||
chr4:89827710 | A | G | 2 | a0001c0001t0013g0140 a0001c0001t0013g0141 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.163+433T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827710 | |||||||
chr4:89827807 | A | ACT | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+334_163+335dup others(2): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827807 | |||||||
chr4:89827815 | T | A | 58 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0002g0002 others(55): Show |
63 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.163+328A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827815 | |||||||
chr4:89827937 | T | C | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+206A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827937 | |||||||
chr4:89827981 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+162T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 3/5 | chr4 | 89827981 | |||||||
chr4:89828217 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | NA18975.hp1 NA18980.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.122-33C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828217 | |||||||
chr4:89828284 | T | G | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-100A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828284 | |||||||
chr4:89828312 | G | GAAAAA | 21 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(18): Show |
23 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.122-133_122-129dup others(5): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828312 | |||||||
chr4:89828320 | T | A | 2 | a0001c0001t0001g0086 a0001c0001t0034g0319 |
2 | HG00741.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.122-136A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828320 | |||||||
chr4:89828356 | CAG | C | 79 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0001g0251 others(76): Show |
85 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.122-174_122-173del others(2): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828356 | |||||||
chr4:89828486 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.122-302T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828486 | |||||||
chr4:89828535 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-351T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828535 | |||||||
chr4:89828644 | TA | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(237): Show |
252 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.122-461delT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828644 | |||||||
chr4:89828651 | AAC | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-469_122-468del others(2): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828651 | |||||||
chr4:89828708 | G | A | 51 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(48): Show |
54 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.122-524C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828708 | |||||||
chr4:89828801 | C | A | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-617G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828801 | |||||||
chr4:89828815 | C | T | 62 | a0001c0001t0001g0040 a0001c0001t0002g0005 a0001c0001t0002g0006 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.122-631G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828815 | |||||||
chr4:89828850 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-666C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828850 | |||||||
chr4:89828871 | A | T | 1 | a0001c0001t0002g0233 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.122-687T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828871 | |||||||
chr4:89828874 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(237): Show |
252 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.122-690G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828874 | |||||||
chr4:89828892 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-708T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828892 | |||||||
chr4:89828991 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.122-807T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89828991 | |||||||
chr4:89829018 | G | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-834C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829018 | |||||||
chr4:89829022 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-838A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829022 | |||||||
chr4:89829074 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-890G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829074 | |||||||
chr4:89829175 | A | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(260): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.122-991T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829175 | |||||||
chr4:89829437 | A | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(260): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.122-1253T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829437 | |||||||
chr4:89829439 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-1255T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829439 | |||||||
chr4:89829571 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-1387T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829571 | |||||||
chr4:89829693 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(259): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.122-1509G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829693 | |||||||
chr4:89829723 | A | G | 1 | a0001c0001t0003g0151 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.122-1539T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829723 | |||||||
chr4:89829807 | T | C | 2 | a0001c0001t0003g0119 a0001c0001t0003g0120 |
2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.122-1623A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829807 | |||||||
chr4:89829823 | G | A | 1 | a0001c0001t0015g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-1639C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829823 | |||||||
chr4:89829836 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.122-1652A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829836 | |||||||
chr4:89829958 | T | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-1774A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89829958 | |||||||
chr4:89830019 | G | C | 1 | a0001c0001t0002g0003 | 3 | NA18940.hp2 NA18941.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.122-1835C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830019 | |||||||
chr4:89830085 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.122-1901G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830085 | |||||||
chr4:89830264 | C | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-2080G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830264 | |||||||
chr4:89830504 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-2320A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830504 | |||||||
chr4:89830550 | C | A | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.122-2366G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830550 | |||||||
chr4:89830657 | A | G | 1 | a0001c0001t0031g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-2473T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830657 | |||||||
chr4:89830802 | A | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.122-2618T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830802 | |||||||
chr4:89830900 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG01071.hp1 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.122-2716G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830900 | |||||||
chr4:89830988 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.122-2804T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89830988 | |||||||
chr4:89831054 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(293): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.122-2870A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831054 | |||||||
chr4:89831100 | G | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0008g0218 |
3 | NA18949.hp1 NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.122-2916C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831100 | |||||||
chr4:89831212 | T | A | 1 | a0001c0001t0026g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.122-3028A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831212 | |||||||
chr4:89831431 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-3247T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831431 | |||||||
chr4:89831495 | C | A | 62 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0002g0005 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.122-3311G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831495 | |||||||
chr4:89831519 | A | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-3335T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831519 | |||||||
chr4:89831822 | G | GA | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-3639_122-3638i others(3): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831822 | |||||||
chr4:89831917 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+3630T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831917 | |||||||
chr4:89831975 | G | A | 5 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+3572C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89831975 | |||||||
chr4:89832029 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.121+3518T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832029 | |||||||
chr4:89832072 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.121+3475C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832072 | |||||||
chr4:89832093 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+3454A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832093 | |||||||
chr4:89832188 | A | T | 5 | a0001c0001t0001g0299 a0001c0001t0010g0294 a0001c0001t0010g0297 others(2): Show |
5 | HG01099.hp1 HG01361.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+3359T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832188 | |||||||
chr4:89832239 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.121+3308G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832239 | |||||||
chr4:89832326 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+3221C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832326 | |||||||
chr4:89832340 | T | C | 1 | a0001c0001t0009g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.121+3207A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832340 | |||||||
chr4:89832489 | A | G | 4 | a0001c0001t0007g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(1): Show |
4 | HG01167.hp2 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+3058T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832489 | |||||||
chr4:89832809 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2738G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832809 | |||||||
chr4:89832814 | A | T | 1 | a0001c0001t0004g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.121+2733T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832814 | |||||||
chr4:89832871 | C | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2676G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832871 | |||||||
chr4:89832952 | A | T | 1 | a0001c0001t0034g0319 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.121+2595T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832952 | |||||||
chr4:89832960 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2587T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832960 | |||||||
chr4:89832993 | C | T | 2 | a0001c0001t0013g0140 a0001c0001t0013g0141 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.121+2554G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89832993 | |||||||
chr4:89833002 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2545A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833002 | |||||||
chr4:89833141 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(236): Show |
251 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.121+2406A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833141 | |||||||
chr4:89833162 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(259): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.121+2385G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833162 | |||||||
chr4:89833184 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121+2363C>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833184 | |||||||
chr4:89833185 | C | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2362G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833185 | |||||||
chr4:89833290 | A | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp2 HG00741.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+2257T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833290 | |||||||
chr4:89833406 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2141C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833406 | |||||||
chr4:89833471 | A | AT | 6 | a0001c0001t0001g0138 a0001c0001t0002g0028 a0001c0001t0005g0029 others(3): Show |
6 | HG03098.hp2 HG03516.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+2075dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833471 | |||||||
chr4:89833471 | A | ATTTT | 20 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(17): Show |
22 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+2072_121+2075d others(6): Show |
SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833471 | |||||||
chr4:89833481 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(256): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.121+2066G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833481 | |||||||
chr4:89833540 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2007T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833540 | |||||||
chr4:89833620 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.121+1927T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833620 | |||||||
chr4:89833677 | A | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+1870T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833677 | |||||||
chr4:89833723 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.121+1824T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833723 | |||||||
chr4:89833804 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01978.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+1743G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833804 | |||||||
chr4:89833887 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.121+1660T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833887 | |||||||
chr4:89833939 | A | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+1608T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89833939 | |||||||
chr4:89834026 | A | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+1521T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834026 | |||||||
chr4:89834040 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121+1507T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834040 | |||||||
chr4:89834049 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.121+1498T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834049 | |||||||
chr4:89834064 | C | T | 1 | a0001c0001t0025g0296 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121+1483G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834064 | |||||||
chr4:89834074 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+1473A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834074 | |||||||
chr4:89834088 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+1459C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834088 | |||||||
chr4:89834236 | T | C | 2 | a0001c0001t0006g0078 a0001c0001t0006g0079 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.121+1311A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834236 | |||||||
chr4:89834252 | T | C | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01099.hp2 HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.121+1295A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834252 | |||||||
chr4:89834275 | A | G | 1 | a0001c0001t0008g0295 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.121+1272T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834275 | |||||||
chr4:89834454 | G | GA | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+1092dupT | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834454 | |||||||
chr4:89834458 | A | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA18943.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.121+1089T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834458 | |||||||
chr4:89834579 | G | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+968C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834579 | |||||||
chr4:89834607 | A | T | 1 | a0001c0001t0005g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+940T>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834607 | |||||||
chr4:89834721 | C | T | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | NA18971.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.121+826G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834721 | |||||||
chr4:89834754 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.121+793C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834754 | |||||||
chr4:89834758 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(236): Show |
251 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.121+789C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834758 | |||||||
chr4:89834788 | A | G | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+759T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834788 | |||||||
chr4:89834926 | T | G | 62 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0002g0005 others(59): Show |
65 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.121+621A>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89834926 | |||||||
chr4:89835040 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+507G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89835040 | |||||||
chr4:89835270 | G | C | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+277C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89835270 | |||||||
chr4:89835382 | C | T | 2 | a0001c0001t0016g0277 a0001c0001t0016g0278 |
2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.121+165G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89835382 | |||||||
chr4:89835399 | C | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(236): Show |
251 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.121+148G>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89835399 | |||||||
chr4:89835475 | C | T | 1 | a0001c0001t0007g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.121+72G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 2/5 | chr4 | 89835475 | |||||||
chr4:89836001 | G | A | 1 | a0001c0001t0020g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-25-309C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836001 | |||||||
chr4:89836121 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(236): Show |
251 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-25-429C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836121 | |||||||
chr4:89836143 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-25-451T>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836143 | |||||||
chr4:89836158 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(258): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-25-466T>C | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836158 | |||||||
chr4:89836161 | C | T | 57 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0001g0251 others(54): Show |
62 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-25-469G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836161 | |||||||
chr4:89836243 | G | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(236): Show |
251 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-25-551C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836243 | |||||||
chr4:89836281 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-25-589C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836281 | |||||||
chr4:89836354 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(260): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-26+608A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836354 | |||||||
chr4:89836433 | T | A | 1 | a0001c0001t0035g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-26+529A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836433 | |||||||
chr4:89836464 | C | T | 1 | a0001c0001t0030g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-26+498G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836464 | |||||||
chr4:89836584 | C | A | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-26+378G>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836584 | |||||||
chr4:89836663 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-26+299G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836663 | |||||||
chr4:89836689 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(264): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.-26+273A>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836689 | |||||||
chr4:89836692 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-26+270C>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836692 | |||||||
chr4:89836694 | C | T | 22 | a0001c0001t0001g0299 a0001c0001t0003g0014 a0001c0001t0004g0015 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-26+268G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836694 | |||||||
chr4:89836790 | C | CT | 61 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0002g0005 others(58): Show |
64 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-26+171dupA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836790 | |||||||
chr4:89836790 | CT | C | 5 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0003g0224 others(2): Show |
5 | HG01261.hp1 HG01516.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+171delA | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836790 | |||||||
chr4:89836796 | T | A | 22 | a0001c0001t0001g0299 a0001c0001t0002g0313 a0001c0001t0002g0314 others(19): Show |
24 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-26+166A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836796 | |||||||
chr4:89836797 | T | A | 100 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0001g0251 others(97): Show |
108 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-26+165A>T | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836797 | |||||||
chr4:89836899 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-26+63G>A | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836899 | |||||||
chr4:89836921 | G | C | 4 | a0001c0001t0014g0316 a0001c0001t0014g0317 a0001c0001t0014g0318 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+41C>G | SNCA | ENSG00000145335.17 | transcript | ENST00000394991.8 | protein_coding | 1/5 | chr4 | 89836921 |