Product Details

SNP ID

rs12971466

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38395589 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCGGCTACGAGGATTACCGGCGCT[C/T]CGGGCCACCCGCGCCCCTCGCCCTG

Phenotype

MIM: 609966 MIM: 609293

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM98C PubMed Links

Gene Details

Gene

FAM98C

Gene Name

family with sequence similarity 98 member C

There are no transcripts associated with this gene.

Gene

GGN

Gene Name

gametogenetin

There are no transcripts associated with this gene.

Gene

SPRED3

Gene Name

sprouty related EVH1 domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042522.2	780	Missense Mutation	TCC,TTC	S226F	NP_001035987.1
XM_006723219.3	780	Missense Mutation	TCC,TTC	S226F	XP_006723282.1
XM_011526978.2	780	Missense Mutation	TCC,TTC	S195F	XP_011525280.1

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