Full data view for gene AIFM1

Information The variants shown are described using the NM_004208.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.1097A>G r.(?) p.(Asn366Ser) Unknown - likely benign g.129270685T>C g.130136710T>C AIFM1(NM_004208.3):c.1097A>G (p.N366S) - AIFM1_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/+? 11 c.1097A>G r.(?) p.(Asn366Ser) Parent #1 - likely pathogenic g.129270685T>C g.130136710T>C - - AIFM1_000040 - MORL Deafness Variation Database - - SUMMARY record - - - 0 - DNA ? - - deafness - - - - - - - - 0 - - 1 Global Variome, with Curator vacancy
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