Unique variants in gene A2M

Information The variants shown are described using the NM_000014.4 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. 1 - c.-28T>G benign r.(=) p.(=) g.9268473A>C - A2M:c.-28T>G - A2M_000005 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
-/. 1 - c.1104+11T>C benign r.(=) p.(=) g.9258821A>G - A2M:c.1104+11T>C - A2M_000004 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
-/. 1 - c.1915A>G benign r.(?) p.(Asn639Asp) g.9248233T>C - A2M:c.1915A>G (N639D) - A2M_000003 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
?/. 1 - c.2359C>T VUS r.(?) p.(Arg787*) g.9243907G>A - A2M:NM_000014.4:c.2359C>T - A2M_000002 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-/. 1 - c.2998A>G benign r.(?) p.(Ile1000Val) g.9232268T>C - A2M:c.2998A>G (I1000V) - A2M_000001 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
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