Product Details

SNP ID

rs12221499

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:22626811 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGGAAGAGAAACAAATTTAAAAG[A/G]GGGGAAGAGTCATTTTTCATTTATT

Phenotype

MIM: 613897 MIM: 602835

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FANCF PubMed Links

Gene Details

Gene

FANCF

Gene Name

Fanconi anemia complementation group F

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022725.3	699	Intron			NP_073562.1

Gene

GAS2

Gene Name

growth arrest specific 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143830.1	699	Intron			NP_001137302.1
NM_005256.3	699	Intron			NP_005247.1
NM_177553.2	699	Intron			NP_808221.1
XM_011519971.2	699	Intron			XP_011518273.1
XM_011519972.2	699	UTR 5			XP_011518274.1
XM_011519975.1	699	Intron			XP_011518277.1
XM_011519978.2	699	Intron			XP_011518280.1
XM_017017528.1	699	Intron			XP_016873017.1
XM_017017529.1	699	Intron			XP_016873018.1
XM_017017530.1	699	Intron			XP_016873019.1
XM_017017531.1	699	Intron			XP_016873020.1
XM_017017532.1	699	Intron			XP_016873021.1

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