Product Details

Primer Sequences
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Primer Chromosome Location
Chr.9: 35075911-35076052 on Build GRCh38
Format
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer™ Tool Quick Reference
Ampliseq ID's

Gene Details

Gene Symbol
FANCG
Entrez Gene ID
2189
Gene Name
Fanconi anemia complementation group G
Gene Aliases
FAG, XRCC9
UniGene
Hs.591084
Gene Chromosome Location
Chr.9: 35073838-35080016 on Build GRCh38
Transcripts
NM_004629.1

Cosmic Detail

Cosmic ID Mutation AA Transcript Location
269145 c.1095G>T p.E365D Chr.9: 35076010-35076010 on Build GRCh38
6227773 c.1087G>A p.A363T Chr.9: 35076018-35076018 on Build GRCh38
1206504 c.1078G>A p.A360T Chr.9: 35076027-35076027 on Build GRCh38
7299764 c.1134G>A p.S378S Chr.9: 35075971-35075971 on Build GRCh38
79834 c.1101C>T p.Y367Y Chr.9: 35076004-35076004 on Build GRCh38
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SNP Detail

SNP ID Chromosome Location
rs746613002 Chr.9: 35076005-35076005 on Build GRCh38
rs4986939 Chr.9: 35075972-35075972 on Build GRCh38
rs746071696 Chr.9: 35075929-35075929 on Build GRCh38
rs767735303 Chr.9: 35075944-35075944 on Build GRCh38
rs768324970 Chr.9: 35076018-35076018 on Build GRCh38
rs756519272 Chr.9: 35075955-35075955 on Build GRCh38
rs778328620 Chr.9: 35075957-35075957 on Build GRCh38
rs376623996 Chr.9: 35076019-35076019 on Build GRCh38
rs571020770 Chr.9: 35075932-35075932 on Build GRCh38
rs779584598 Chr.9: 35076001-35076001 on Build GRCh38
rs1007569856 Chr.9: 35075951-35075951 on Build GRCh38
rs530574134 Chr.9: 35075971-35075971 on Build GRCh38
rs889089609 Chr.9: 35075931-35075931 on Build GRCh38
rs567518139 Chr.9: 35076025-35076025 on Build GRCh38
rs753111489 Chr.9: 35075945-35075945 on Build GRCh38
rs769547477 Chr.9: 35076030-35076030 on Build GRCh38
rs759859786 Chr.9: 35075935-35075935 on Build GRCh38
rs901079231 Chr.9: 35076028-35076028 on Build GRCh38

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