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SNP ID

rs104893636

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:176151875 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCCTGCGCGGGGTCACGGACAAG[A/T]GCCAGGCGGCCCCGGCGGTCACTAC

Phenotype

MIM: 142980 MIM: 142981 MIM: 611576

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

HOXD3 PubMed Links

Gene Details

Gene

HOXD3

Gene Name

homeobox D3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006898.4	1482	Intron			NP_008829.3
XM_005246509.3	1482	Intron			XP_005246566.1
XM_005246510.4	1482	Intron			XP_005246567.1
XM_005246511.3	1482	Intron			XP_005246568.1
XM_005246513.4	1482	Intron			XP_005246570.1
XM_006712477.2	1482	Intron			XP_006712540.1
XM_011511065.2	1482	Intron			XP_011509367.1
XM_011511066.2	1482	Intron			XP_011509368.1

Gene

HOXD4

Gene Name

homeobox D4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014621.2	1482	Missense Mutation	GAG,GTG	E81V	NP_055436.2
XM_005246514.4	1482	Missense Mutation	GAG,GTG	E81V	XP_005246571.1

Gene

MIR10B

Gene Name

microRNA 10b

There are no transcripts associated with this gene.

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