Product Details

SNP ID
rs141209316
Assay Type
Functionally Tested
NCBI dbSNP Submissions
4
Location
Chr.1:24651492 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGCGCAGTCATTCTCGATCTCCCC[A/G]TCACAGAACCAAGAGCCGGAGTCCT
Phenotype
MIM: 605975
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SRRM1 PubMed Links

Gene Details

Gene
SRRM1
Gene Name
serine and arginine repetitive matrix 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303448.1 2700 Missense Mutation CAT,CGT H202R NP_001290377.1
NM_001303449.1 2700 Intron NP_001290378.1
NM_005839.3 2700 Missense Mutation CAT,CGT H202R NP_005830.2
XM_005245717.2 2700 Intron XP_005245774.1
XM_005245718.2 2700 Intron XP_005245775.1
XM_005245720.2 2700 Intron XP_005245777.1
XM_005245721.2 2700 Intron XP_005245778.1
XM_005245722.2 2700 Intron XP_005245779.1
XM_011540478.2 2700 Intron XP_011538780.1
XM_011540479.1 2700 Missense Mutation CAT,CGT H119R XP_011538781.1
XM_011540480.1 2700 Missense Mutation CAT,CGT H119R XP_011538782.1
XM_011540481.1 2700 Missense Mutation CAT,CGT H119R XP_011538783.1
XM_011540482.1 2700 Missense Mutation CAT,CGT H119R XP_011538784.1
XM_011540483.1 2700 Intron XP_011538785.1
XM_017000011.1 2700 Intron XP_016855500.1
XM_017000012.1 2700 Intron XP_016855501.1
XM_017000013.1 2700 Intron XP_016855502.1
XM_017000014.1 2700 Intron XP_016855503.1
XM_017000015.1 2700 Intron XP_016855504.1
XM_017000016.1 2700 Intron XP_016855505.1
XM_017000017.1 2700 Intron XP_016855506.1
XM_017000018.1 2700 Intron XP_016855507.1
XM_017000019.1 2700 Intron XP_016855508.1
XM_017000020.1 2700 Intron XP_016855509.1
XM_017000021.1 2700 Intron XP_016855510.1
XM_017000022.1 2700 Intron XP_016855511.1
XM_017000023.1 2700 Missense Mutation CAT,CGT H119R XP_016855512.1
XM_017000024.1 2700 Missense Mutation CAT,CGT H119R XP_016855513.1
XM_017000025.1 2700 Intron XP_016855514.1
XM_017000026.1 2700 Intron XP_016855515.1
XM_017000027.1 2700 Missense Mutation CAT,CGT H119R XP_016855516.1
XM_017000028.1 2700 Missense Mutation CAT,CGT H119R XP_016855517.1
XM_017000029.1 2700 Missense Mutation CAT,CGT H119R XP_016855518.1
XM_017000030.1 2700 Intron XP_016855519.1
XM_017000031.1 2700 Intron XP_016855520.1
XM_017000032.1 2700 Intron XP_016855521.1
XM_017000033.1 2700 Intron XP_016855522.1
XM_017000034.1 2700 Intron XP_016855523.1

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