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SNP ID

rs150961638

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:13042939 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATACCTGCAATATCTTCTAGCTCCT[C/T]GGTATCAACCCTGTAACAAAAAGTT

Phenotype

MIM: 300479

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM9C PubMed Links

Gene Details

Gene

FAM9C

Gene Name

family with sequence similarity 9 member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174901.5	520	Missense Mutation	AAG,GAG	K65E	NP_777561.1
XM_005274460.2	520	Intron			XP_005274517.1
XM_017029321.1	520	Intron			XP_016884810.1

Gene

LOC105373133

Gene Name

uncharacterized LOC105373133

There are no transcripts associated with this gene.

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