Allele Frequency | HGVD

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Allele Frequency Allele Color Code:

:A

:G

:C

:T

:Others
Variation Color Code:

:nonsense, splice

:missense

:synonymous

:indel

:non-coding, intron, other

Variant position	rsID	Ref/Alt	Frequency of alternative allele	Genotype count			Number of Samples Covered	Average sample read depth	Alleles	Gene	mRNA Accession#	Function				Org	Platform
				Genotype count								Codon		AA
				Ref/Ref	Ref/Alt	Alt/Alt						Ref	Alt	Ref	Alt
chr2:218712875	unknown	G/A	0.0001	4342	1	0	4343	49.54±60.08	0.9999 0.0001	TNS1	NM_022648	CCA	TCA	Pro	Ser	All
chr2:218712875	unknown	G/.	0.0000	300	0	0	300	97.52±68.09	1.0000 0	TNS1	NM_022648	CCA	TCA	Pro	Ser	KU	HiSeq + SOLiD
chr2:218712875	unknown	G/.	0.0000	429	0	0	429	169.79±38.29	1.0000 0	TNS1	NM_022648	CCA	TCA	Pro	Ser	YCU	HiSeq
chr2:218712875	unknown	G/.	0.0000	70	0	0	70	142.04±51.74	1.0000 0	TNS1	NM_022648	CCA	TCA	Pro	Ser	NCCHD	HiSeq
chr2:218712875	unknown	G/.	0.0000	38	0	0	38	242.71±80.26	1.0000 0	TNS1	NM_022648	CCA	TCA	Pro	Ser	TU	HiSeq
chr2:218712875	unknown	G/.	0.0000	371	0	0	371	98.39±28.21	1.0000 0	TNS1	NM_022648	CCA	TCA	Pro	Ser	UT	HiSeq
chr2:218712875	unknown	G/A	0.0002	3134	1	0	3135	18.27±5.1	0.9998 0.0002	TNS1	NM_022648	CCA	TCA	Pro	Ser	KU+RIKEN	HiSeqX