Product Details

SNP ID

rs199609262

Assay Type

Functionally tested

NCBI dbSNP Submissions

9

Location

Chr.1:43995659 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCCTCTGAGGCAGCCCTGGAGC[C/G]CACCCTGGCAGGTGAGGACACGGAG

Phenotype

MIM: 604013 MIM: 601019

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

B4GALT2 PubMed Links

Gene Details

Gene

B4GALT2

Gene Name

beta-1,4-galactosyltransferase 2

There are no transcripts associated with this gene.

Gene

CCDC24

Gene Name

coiled-coil domain containing 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152499.2	645	Missense Mutation	CCC,CGC	P204R	NP_689712.1
XM_017000423.1	645	Missense Mutation	CCC,CGC	P285R	XP_016855912.1
XM_017000424.1	645	Missense Mutation	CCC,CGC	P285R	XP_016855913.1
XM_017000425.1	645	Missense Mutation	CCC,CGC	P285R	XP_016855914.1
XM_017000426.1	645	Missense Mutation	CCC,CGC	P254R	XP_016855915.1
XM_017000427.1	645	Missense Mutation	CCC,CGC	P253R	XP_016855916.1
XM_017000428.1	645	Missense Mutation	CCC,CGC	P252R	XP_016855917.1
XM_017000429.1	645	Missense Mutation	CCC,CGC	P249R	XP_016855918.1
XM_017000430.1	645	Missense Mutation	CCC,CGC	P252R	XP_016855919.1
XM_017000431.1	645	Missense Mutation	CCC,CGC	P216R	XP_016855920.1
XM_017000432.1	645	Missense Mutation	CCC,CGC	P205R	XP_016855921.1
XM_017000433.1	645	Missense Mutation	CCC,CGC	P204R	XP_016855922.1
XM_017000434.1	645	Missense Mutation	CCC,CGC	P203R	XP_016855923.1
XM_017000435.1	645	Missense Mutation	CCC,CGC	P200R	XP_016855924.1
XM_017000436.1	645	Missense Mutation	CCC,CGC	P200R	XP_016855925.1
XM_017000437.1	645	Missense Mutation	CCC,CGC	P186R	XP_016855926.1
XM_017000438.1	645	Missense Mutation	CCC,CGC	P181R	XP_016855927.1
XM_017000439.1	645	Missense Mutation	CCC,CGC	P173R	XP_016855928.1
XM_017000440.1	645	Missense Mutation	CCC,CGC	P168R	XP_016855929.1
XM_017000441.1	645	Missense Mutation	CCC,CGC	P168R	XP_016855930.1
XM_017000442.1	645	Missense Mutation	CCC,CGC	P128R	XP_016855931.1
XM_017000443.1	645	Intron			XP_016855932.1
XM_017000444.1	645	Intron			XP_016855933.1
XM_017000445.1	645	Missense Mutation	CCC,CGC	P71R	XP_016855934.1
XM_017000446.1	645	Missense Mutation	CCC,CGC	P70R	XP_016855935.1

Gene

SLC6A9

Gene Name

solute carrier family 6 member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024845.2	645	Intron			NP_001020016.1
NM_001261380.1	645	Intron			NP_001248309.1
NM_006934.3	645	Intron			NP_008865.2
NM_201649.3	645	Intron			NP_964012.2
XM_011542017.2	645	Intron			XP_011540319.1
XM_017002151.1	645	Intron			XP_016857640.1
XM_017002152.1	645	Intron			XP_016857641.1
XM_017002153.1	645	Intron			XP_016857642.1

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