Product Details

SNP ID
rs6419802
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:75911147 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAATTTGCAACCAAATAGGACAAAT[A/G]TGTTGAACTGTACTTTTCTTGAAGA
Phenotype
MIM: 602431
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ROBO2 PubMed Links

Gene Details

Gene
ROBO2
Gene Name
roundabout guidance receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128929.3 Intron NP_001122401.1
NM_001290039.1 Intron NP_001276968.1
NM_001290040.1 Intron NP_001276969.1
NM_001290065.1 Intron NP_001276994.1
NM_002942.4 Intron NP_002933.1
XM_011533981.2 Intron XP_011532283.1
XM_011533982.1 Intron XP_011532284.1
XM_011533983.1 Intron XP_011532285.1
XM_011533984.1 Intron XP_011532286.1
XM_011533985.1 Intron XP_011532287.1
XM_017006986.1 Intron XP_016862475.1
XM_017006987.1 Intron XP_016862476.1
XM_017006988.1 Intron XP_016862477.1
XM_017006989.1 Intron XP_016862478.1
XM_017006990.1 Intron XP_016862479.1
XM_017006991.1 Intron XP_016862480.1
XM_017006992.1 Intron XP_016862481.1
XM_017006993.1 Intron XP_016862482.1
XM_017006994.1 Intron XP_016862483.1
XM_017006995.1 Intron XP_016862484.1
XM_017006996.1 Intron XP_016862485.1
XM_017006997.1 Intron XP_016862486.1
XM_017006998.1 Intron XP_016862487.1
XM_017006999.1 Intron XP_016862488.1
XM_017007000.1 Intron XP_016862489.1
XM_017007001.1 Intron XP_016862490.1
XM_017007002.1 Intron XP_016862491.1
XM_017007003.1 Intron XP_016862492.1
XM_017007004.1 Intron XP_016862493.1
XM_017007005.1 Intron XP_016862494.1
XM_017007006.1 Intron XP_016862495.1

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