Product Details

SNP ID

rs6624562

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:71600353 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAACTTCAGCTACCATTTACTAT[C/T]TTTGTAATTTTGTAAAGAACACCAA

Phenotype

MIM: 300369

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ACRC PubMed Links

Gene Details

Gene

ACRC

Gene Name

acidic repeat containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052957.4		Intron			NP_443189.1
XM_006724716.3		Intron			XP_006724779.1
XM_011531063.2		Intron			XP_011529365.1
XM_011531064.1		Intron			XP_011529366.1
XM_011531066.2		Intron			XP_011529368.1
XM_011531067.2		Intron			XP_011529369.1
XM_017029965.1		Intron			XP_016885454.1

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