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SNP ID: rs1047948
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.2:55290355 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: GCTCTCAAGTTAAAAAAATGCACAC[A/G]CATACATAACCCAATACCAAAGAAA
Phenotype: MIM: 609736
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CCDC88A PubMed Links

Gene Details

Gene: CCDC88A
Gene Name: coiled-coil domain containing 88A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135597.1	6925	UTR 3			NP_001129069.1
NM_001254943.1	6925	UTR 3			NP_001241872.1
NM_018084.4	6925	UTR 3			NP_060554.3
XM_005264418.4	6925	Intron			XP_005264475.1
XM_005264421.2	6925	UTR 3			XP_005264478.1
XM_005264426.2	6925	Intron			XP_005264483.1
XM_011532965.2	6925	UTR 3			XP_011531267.1
XM_011532966.2	6925	Intron			XP_011531268.1
XM_011532967.2	6925	Intron			XP_011531269.1
XM_011532968.2	6925	UTR 3			XP_011531270.1
XM_017004476.1	6925	Intron			XP_016859965.1
XM_017004477.1	6925	Intron			XP_016859966.1
XM_017004478.1	6925	Intron			XP_016859967.1
XM_017004479.1	6925	Intron			XP_016859968.1
XM_017004480.1	6925	Intron			XP_016859969.1
XM_017004481.1	6925	Intron			XP_016859970.1

Gene: PRORSD1P
Gene Name: prolyl-tRNA synthetase associated domain containing 1, pseudogene

There are no transcripts associated with this gene.

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