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SNP ID: rs147704347
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:2590477 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGCACTTGGGGGCATCCTGGTCAC[C/T]GCTGGCCCTAGCATTGGACCCTAGG
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: FAM213B PubMed Links

Gene Details

Gene: FAM213B
Gene Name: family with sequence similarity 213 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195736.1	1751	UTR 3			NP_001182665.1
NM_001195737.1	1751	UTR 3			NP_001182666.1
NM_001195738.1	1751	UTR 3			NP_001182667.1
NM_001195740.1	1751	UTR 3			NP_001182669.1
NM_001195741.1	1751	UTR 3			NP_001182670.1
NM_152371.3	1751	UTR 3			NP_689584.2
XM_006710354.3	1751	UTR 3			XP_006710417.1
XM_011540664.1	1751	UTR 3			XP_011538966.1
XM_011540665.1	1751	UTR 3			XP_011538967.1
XM_011540666.1	1751	UTR 3			XP_011538968.1

Gene: LOC100996583
Gene Name: uncharacterized LOC100996583

There are no transcripts associated with this gene.

Gene: MMEL1
Gene Name: membrane metallo-endopeptidase-like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033467.3	1751	Intron			NP_258428.2
XM_011542122.2	1751	Intron			XP_011540424.1
XM_017002310.1	1751	Intron			XP_016857799.1
XM_017002311.1	1751	Intron			XP_016857800.1
XM_017002312.1	1751	Intron			XP_016857801.1
XM_017002313.1	1751	Intron			XP_016857802.1
XM_017002314.1	1751	Intron			XP_016857803.1
XM_017002315.1	1751	Intron			XP_016857804.1

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