Product Details
- SNP ID
-
rs34024439
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:47853267 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCACTGGCTGAAGTGGGGGCGCCA[C/G]CTTCAGGCGCTGCCTCAGAGATGGC
- Phenotype
-
MIM: 616423
MIM: 157132
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
DHX30
PubMed Links
Gene Details
- Gene
- DHX30
- Gene Name
- DEAH-box helicase 30
There are no transcripts associated with this gene.
- Gene
- MAP4
- Gene Name
- microtubule associated protein 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001134364.1 |
3917 |
Intron |
|
|
NP_001127836.1 |
NM_002375.4 |
3917 |
Missense Mutation |
GCT,GGT |
A1116G |
NP_002366.2 |
NM_030885.3 |
3917 |
Intron |
|
|
NP_112147.2 |
XM_005265133.4 |
3917 |
Missense Mutation |
GCT,GGT |
A2278G |
XP_005265190.1 |
XM_005265134.4 |
3917 |
Missense Mutation |
GCT,GGT |
A2278G |
XP_005265191.1 |
XM_005265155.4 |
3917 |
Missense Mutation |
GCT,GGT |
A1093G |
XP_005265212.1 |
XM_005265157.4 |
3917 |
Missense Mutation |
GCT,GGT |
A939G |
XP_005265214.1 |
XM_005265158.2 |
3917 |
Missense Mutation |
GCT,GGT |
A870G |
XP_005265215.1 |
XM_006713146.3 |
3917 |
Missense Mutation |
GCT,GGT |
A2290G |
XP_006713209.1 |
XM_006713147.3 |
3917 |
Missense Mutation |
GCT,GGT |
A2290G |
XP_006713210.1 |
XM_006713152.3 |
3917 |
Missense Mutation |
GCT,GGT |
A2273G |
XP_006713215.1 |
XM_011533703.2 |
3917 |
Missense Mutation |
GCT,GGT |
A2290G |
XP_011532005.1 |
XM_011533704.2 |
3917 |
Missense Mutation |
GCT,GGT |
A2275G |
XP_011532006.1 |
XM_011533705.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2273G |
XP_011532007.1 |
XM_011533708.2 |
3917 |
Missense Mutation |
GCT,GGT |
A2258G |
XP_011532010.1 |
XM_011533709.2 |
3917 |
Missense Mutation |
GCT,GGT |
A2252G |
XP_011532011.1 |
XM_011533710.2 |
3917 |
Missense Mutation |
GCT,GGT |
A2249G |
XP_011532012.1 |
XM_011533718.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2204G |
XP_011532020.1 |
XM_011533719.2 |
3917 |
Missense Mutation |
GCT,GGT |
A1145G |
XP_011532021.1 |
XM_017006391.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2275G |
XP_016861880.1 |
XM_017006392.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2252G |
XP_016861881.1 |
XM_017006393.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2273G |
XP_016861882.1 |
XM_017006394.1 |
3917 |
Missense Mutation |
GCT,GGT |
A2232G |
XP_016861883.1 |
XM_017006395.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1145G |
XP_016861884.1 |
XM_017006396.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1130G |
XP_016861885.1 |
XM_017006397.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1130G |
XP_016861886.1 |
XM_017006398.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1128G |
XP_016861887.1 |
XM_017006399.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1133G |
XP_016861888.1 |
XM_017006400.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1133G |
XP_016861889.1 |
XM_017006401.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1092G |
XP_016861890.1 |
XM_017006402.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1116G |
XP_016861891.1 |
XM_017006403.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1076G |
XP_016861892.1 |
XM_017006404.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1076G |
XP_016861893.1 |
XM_017006405.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1101G |
XP_016861894.1 |
XM_017006406.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1095G |
XP_016861895.1 |
XM_017006407.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1061G |
XP_016861896.1 |
XM_017006408.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1061G |
XP_016861897.1 |
XM_017006409.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1078G |
XP_016861898.1 |
XM_017006410.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1077G |
XP_016861899.1 |
XM_017006411.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1075G |
XP_016861900.1 |
XM_017006412.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1075G |
XP_016861901.1 |
XM_017006413.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1047G |
XP_016861902.1 |
XM_017006414.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1047G |
XP_016861903.1 |
XM_017006415.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1032G |
XP_016861904.1 |
XM_017006416.1 |
3917 |
Missense Mutation |
GCT,GGT |
A1006G |
XP_016861905.1 |
XM_017006417.1 |
3917 |
Missense Mutation |
GCT,GGT |
A939G |
XP_016861906.1 |
XM_017006418.1 |
3917 |
Missense Mutation |
GCT,GGT |
A924G |
XP_016861907.1 |
XM_017006419.1 |
3917 |
Missense Mutation |
GCT,GGT |
A901G |
XP_016861908.1 |
XM_017006420.1 |
3917 |
Missense Mutation |
GCT,GGT |
A901G |
XP_016861909.1 |
XM_017006421.1 |
3917 |
Missense Mutation |
GCT,GGT |
A870G |
XP_016861910.1 |
XM_017006422.1 |
3917 |
Missense Mutation |
GCT,GGT |
A855G |
XP_016861911.1 |
- Gene
- MIR1226
- Gene Name
- microRNA 1226
There are no transcripts associated with this gene.
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