Product Details

SNP ID: rs202071453
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:99560686 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCAGGACACCGACATGGAACAGGGA[C/G]TCACTGGGGGTAAGGCAGAGAAAGC
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: FAM200A PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009958.1	364	Missense Mutation	CTC,GTC	L43V	NP_001009958.1
NM_001009960.1	364	Missense Mutation	CTC,GTC	L43V	NP_001009960.1
NM_001083956.1	364	Missense Mutation	CTC,GTC	L43V	NP_001077425.1
NM_001085366.1	364	Missense Mutation	CTC,GTC	L43V	NP_001078835.1
NM_001085367.1	364	Missense Mutation	CTC,GTC	L43V	NP_001078836.1
NM_001085368.1	364	Missense Mutation	CTC,GTC	L43V	NP_001078837.1
NM_024061.3	364	Missense Mutation	CTC,GTC	L43V	NP_076966.1
NM_138494.2	364	Missense Mutation	CTC,GTC	L43V	NP_612503.1
XM_017012598.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868087.1
XM_017012599.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868088.1
XM_017012600.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868089.1
XM_017012601.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868090.1
XM_017012602.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868091.1
XM_017012603.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868092.1
XM_017012604.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868093.1
XM_017012605.1	364	UTR 5			XP_016868094.1
XM_017012606.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868095.1
XM_017012607.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868096.1
XM_017012608.1	364	UTR 5			XP_016868097.1
XM_017012609.1	364	UTR 5			XP_016868098.1
XM_017012610.1	364	UTR 5			XP_016868099.1
XM_017012611.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868100.1
XM_017012612.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868101.1
XM_017012613.1	364	Missense Mutation	CTC,GTC	L43V	XP_016868102.1