Product Details

SNP ID

rs148391785

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:43432492 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACTTCTCCCAGGGCCCATGGCCC[A/G]CCTATGCTTGCTCATCCTGCAGCTG

Phenotype

MIM: 612509

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ABCC10 PubMed Links

Gene Details

Gene

ABCC10

Gene Name

ATP binding cassette subfamily C member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198934.1	727	Missense Mutation	CAC,CGC	H171R	NP_001185863.1
NM_033450.2	727	Missense Mutation	CAC,CGC	H128R	NP_258261.2
XM_011514974.2	727	Missense Mutation	CAC,CGC	H222R	XP_011513276.2
XM_011514983.2	727	Intron			XP_011513285.1
XM_011514985.2	727	Intron			XP_011513287.1
XM_011514986.2	727	Intron			XP_011513288.1
XM_017011445.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866934.1
XM_017011446.1	727	Missense Mutation	CAC,CGC	H171R	XP_016866935.1
XM_017011447.1	727	Missense Mutation	CAC,CGC	H171R	XP_016866936.1
XM_017011448.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866937.1
XM_017011449.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866938.1
XM_017011450.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866939.1
XM_017011451.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866940.1
XM_017011452.1	727	Missense Mutation	CAC,CGC	H3R	XP_016866941.1
XM_017011453.1	727	Missense Mutation	CAC,CGC	H222R	XP_016866942.1
XM_017011454.1	727	Intron			XP_016866943.1
XM_017011455.1	727	Intron			XP_016866944.1
XM_017011456.1	727	Intron			XP_016866945.1

Gene

MIR6780B

Gene Name

microRNA 6780b

There are no transcripts associated with this gene.

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