Variant #0000657164 (NC_000012.11:g.57939824G>A, NM_004984.2:c.-4231G>A (KIF5A))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57939824G>A
DNA change (hg38) g.57546041G>A
Published as DCTN2(NM_001348065.2):c.221C>T (p.A74V)
ISCN -
DB-ID DCTN2_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00023 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF5A NM_004984.2 ?/. - c.-4231G>A r.(?) p.(=)
DCTN2 NM_006400.4 ?/. - c.92C>T r.(?) p.(Ala31Val)
MBD6 NM_052897.3 ?/. - c.*16807G>A r.(=) p.(=)


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