Product Details

SNP ID

rs75282408

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:129842205 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCATTCAAATGTTTTGTTGTGTA[A/C]CTAAAAAAAGAAAAGAAAAAAGATC

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FAM49B PubMed Links

Gene Details

Gene

FAM49B

Gene Name

family with sequence similarity 49 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256763.1	1212	Silent Mutation			NP_001243692.1
NM_016623.4	1212	Silent Mutation			NP_057707.3
XM_005250966.3	1212	Missense Mutation			XP_005251023.1
XM_011517108.2	1212	Missense Mutation			XP_011515410.1
XM_011517109.2	1212	Missense Mutation			XP_011515411.1
XM_011517110.2	1212	Missense Mutation			XP_011515412.1
XM_011517111.2	1212	Missense Mutation			XP_011515413.1
XM_011517112.2	1212	Missense Mutation			XP_011515414.1
XM_011517113.2	1212	Missense Mutation			XP_011515415.1
XM_011517114.2	1212	Missense Mutation			XP_011515416.1
XM_011517115.2	1212	Missense Mutation			XP_011515417.1
XM_011517116.2	1212	Missense Mutation			XP_011515418.1
XM_011517117.2	1212	Missense Mutation			XP_011515419.1
XM_011517118.2	1212	Missense Mutation			XP_011515420.1
XM_011517120.2	1212	Missense Mutation			XP_011515422.1
XM_011517121.2	1212	Missense Mutation			XP_011515423.1
XM_011517122.2	1212	Missense Mutation			XP_011515424.1
XM_011517123.2	1212	Missense Mutation			XP_011515425.1
XM_011517124.2	1212	Missense Mutation			XP_011515426.1
XM_011517125.2	1212	Missense Mutation			XP_011515427.1
XM_017013539.1	1212	Missense Mutation			XP_016869028.1
XM_017013540.1	1212	Missense Mutation			XP_016869029.1
XM_017013541.1	1212	Missense Mutation			XP_016869030.1
XM_017013542.1	1212	Missense Mutation			XP_016869031.1
XM_017013543.1	1212	Missense Mutation			XP_016869032.1
XM_017013544.1	1212	Missense Mutation			XP_016869033.1
XM_017013545.1	1212	Missense Mutation			XP_016869034.1
XM_017013546.1	1212	Missense Mutation			XP_016869035.1
XM_017013547.1	1212	Missense Mutation			XP_016869036.1
XM_017013548.1	1212	Missense Mutation			XP_016869037.1
XM_017013549.1	1212	Missense Mutation			XP_016869038.1
XM_017013550.1	1212	Missense Mutation			XP_016869039.1
XM_017013551.1	1212	Missense Mutation			XP_016869040.1
XM_017013552.1	1212	Missense Mutation			XP_016869041.1
XM_017013553.1	1212	Missense Mutation			XP_016869042.1
XM_017013554.1	1212	Missense Mutation			XP_016869043.1
XM_017013555.1	1212	Missense Mutation			XP_016869044.1
XM_017013556.1	1212	Missense Mutation			XP_016869045.1
XM_017013557.1	1212	Missense Mutation			XP_016869046.1
XM_017013558.1	1212	Missense Mutation			XP_016869047.1
XM_017013559.1	1212	Missense Mutation			XP_016869048.1
XM_017013560.1	1212	Silent Mutation			XP_016869049.1
XM_017013561.1	1212	Missense Mutation			XP_016869050.1
XM_017013562.1	1212	Missense Mutation			XP_016869051.1

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