Variant #0000807747 (NC_000016.9:g.89986614C>T, NM_002386.3:c.948C>T (MC1R))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89986614C>T
DNA change (hg38) -
Published as MC1R(NM_002386.3):c.948C>T (p.S316=), MC1R(NM_002386.4):c.948C>T (p.S316=)
ISCN -
DB-ID MC1R_000034 See all 2 reported entries
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) 0.00171 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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     
MC1R NM_002386.3 -?/. - c.948C>T r.(?) p.(Ser316=)
TUBB3 NM_006086.3 -?/. - c.-3196C>T r.(?) p.(=)


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