Product Details
- SNP ID
-
rs61758784
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:58695161 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AATGAAAACAACAGAAATTTGTGGT[A/G]CACCAGGTGTTGGAAAAACACAATT
- Phenotype
-
MIM: 602774
MIM: 605792
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RAD51C
PubMed Links
Gene Details
- Gene
- RAD51C
- Gene Name
- RAD51 paralog C
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_002876.3 |
418 |
Missense Mutation |
ACA,GCA |
T126A |
NP_002867.1 |
NM_058216.2 |
418 |
Missense Mutation |
ACA,GCA |
T126A |
NP_478123.1 |
XM_006722001.3 |
418 |
Missense Mutation |
ACA,GCA |
T126A |
XP_006722064.1 |
XM_006722002.3 |
418 |
Missense Mutation |
ACA,GCA |
T126A |
XP_006722065.1 |
XM_006722004.3 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_006722067.1 |
XM_006722005.3 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_006722068.1 |
XM_011525092.2 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_011523394.1 |
XM_011525093.2 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_011523395.1 |
XM_011525094.2 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_011523396.1 |
XM_017024914.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880403.1 |
XM_017024915.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880404.1 |
XM_017024916.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880405.1 |
XM_017024917.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880406.1 |
XM_017024918.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880407.1 |
XM_017024919.1 |
418 |
Missense Mutation |
ACA,GCA |
T9A |
XP_016880408.1 |
- Gene
- TEX14
- Gene Name
- testis expressed 14, intercellular bridge forming factor
There are no transcripts associated with this gene.
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