21797713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626980-T-C

http://identifiers.org/hco/16/GRCh38#21797725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13626971-C-A

21797725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626971-C-T

21797759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626943-G-A

21797780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626922-G-A

21797808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626894-G-A

21797808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626894-G-C

21797808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626894-G-T

21797827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626875-C-G

21797840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626862-C-G

21797840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13626862-C-T

21797848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13626854-A-G

21797868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626834-A-T

21797873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626829-A-G

21797878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626824-A-G

21797910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626819-G-A

21797910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626819-G-T

21797911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626818-T-A

21797915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626814-A-G

21797919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626810-C-G

21797919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626810-C-T

http://identifiers.org/hco/16/GRCh38#21797930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13626799-C-A

21797930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626799-C-G

21797930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626799-C-T

21797931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13626798-A-G

21799633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624620-A-G

21799648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 13624607-A-G

21799653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624602-C-T

21799681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624574-G-C

21799688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624567-A-G

21799696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624559-G-T

http://identifiers.org/hco/16/GRCh38#21799710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13624545-C-A

21799710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624545-C-T

21799729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624526-T-C

21799731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624524-G-A

21799738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624517-G-A

21799738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624517-G-T

21799758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624497-C-T

http://identifiers.org/hco/16/GRCh38#21799766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13624489-C-A

21799766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624489-C-T

21799769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624486-G-A

21799778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624477-T-C

21799781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624474-T-C

21799791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624464-T-C

21799821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624434-A-G

21799824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13624431-G-A

http://identifiers.org/hco/16/GRCh38#21799868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13624390-C-A

21799868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624390-C-G

http://identifiers.org/hco/16/GRCh38#21799959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13624200-C-A

21799959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624200-C-G

21799959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624200-C-T

21799979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624158-G-A

21799979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624158-G-C

21800063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13624036-G-A

21800136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623936-G-A

21800137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623935-T-C

21800169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623871-G-A

21800169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623871-G-C

21800320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623673-T-C

21800322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623671-G-C

21800324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623669-T-C

21800557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623257-T-A

21800557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623257-T-C

21800576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623238-G-A

21800576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623238-G-T

21800589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623220-A-G

http://identifiers.org/hco/16/GRCh38#21800598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13623211-A-C

21800598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623211-A-T

21800599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623210-C-T

21800625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623182-G-T

21800667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623012-G-A

21800667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623012-G-T

21800670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13623009-T-C

21800680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622999-A-G

21800689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622959-G-A

21800689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622959-G-T

http://identifiers.org/hco/16/GRCh38#21800706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13622942-C-A

21800706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 13622942-C-T

21800714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622934-A-G

21800714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622934-A-T

21800723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622925-T-C

21800746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622902-A-G

21800764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622884-T-C

21800765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622883-G-A

21800765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622883-G-C

21800765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622883-G-T

21800778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622870-A-G

21800779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622869-G-A

21800779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622869-G-T

21800785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622863-C-T

21800789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622859-G-T

21800799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622849-G-A

21800799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622849-G-T

http://identifiers.org/hco/16/GRCh38#21800805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13622843-C-A

21800805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622843-C-T

21800814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622834-T-A

21800814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622834-T-C

21800827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622821-T-A

21800827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622821-T-C

21800830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622818-G-A

21800830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13622818-G-T

http://identifiers.org/hco/16/GRCh38#21800840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13622808-A-C

21800840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13622808-A-G

21800840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13622808-A-T

21800842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13622806-A-G

21800842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13622806-A-T

21800848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622800-A-G

21800849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622799-G-A

21800849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622799-G-C

21800849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622799-G-T

21800863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622785-G-A

21800863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622785-G-T

http://identifiers.org/hco/16/GRCh38#21800878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13622771-C-A

21800878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622771-C-G

21800894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622755-A-G

21800894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622755-A-T

21800895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13622754-T-C

21802476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13614500-G-A

21802490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13614455-T-C

21802513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13614432-C-G

21802513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13614432-C-T

21802645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13613930-C-T

21802662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13613913-C-T

http://identifiers.org/hco/16/GRCh38#21802674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13613901-A-C

http://identifiers.org/hco/16/GRCh38#21802734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13613841-A-C

21802734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13613841-A-G

21802773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13613811-T-C

21806088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13610949-A-G

21806113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13610926-A-G

21806181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13610858-A-G

21806181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13610858-A-T

21806183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13610856-G-A

21806183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13610856-G-T

21806265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610776-G-A

21806265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610776-G-T

http://identifiers.org/hco/16/GRCh38#21806281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13610766-C-A

21806281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610766-C-T

21806285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610765-T-C

21806325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610726-A-G

21806325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610726-A-T

21806337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13610714-A-G

21809565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609917-A-T

21809572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609910-A-G

21809598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609885-T-C

21809743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609760-T-C

21809826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609696-G-A

21809910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609648-C-T

http://identifiers.org/hco/16/GRCh38#21810090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13609408-C-A

21810111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609382-A-G

21810133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13609360-G-A

http://identifiers.org/hco/16/GRCh38#21810134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13609359-C-A

21810496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13609215-A-T

21810546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13609165-A-G

21810561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13609150-A-G

http://identifiers.org/hco/16/GRCh38#21810571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13609140-C-A

21810571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13609140-C-T

21810577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608783-T-C

21810598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608762-T-C

21810616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608749-G-A

21810616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608749-G-T

21810631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608737-A-T

http://identifiers.org/hco/16/GRCh38#21810665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13608713-A-C

21810668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608710-G-A

21810668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608710-G-C

21810668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608710-G-T

21810719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608665-A-G

21810746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608601-A-G

21810763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608558-A-G

21810764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608557-A-G

21810764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608557-A-T

21810771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608550-T-A

21810771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608550-T-C

21810772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608549-C-T

21810788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608533-T-C

21810811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608510-T-A

21810811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608510-T-C

21810814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608507-T-C

21810822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13608499-A-G

21810864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608458-G-A

21810864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608458-G-T

http://identifiers.org/hco/16/GRCh38#21810870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13608452-C-A

http://identifiers.org/hco/16/GRCh38#21810880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13608440-C-A

21810880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608440-C-G

21810880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608440-C-T

21810886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608434-G-A

21811028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608240-A-G

21811032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608182-C-G

21811046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608170-A-G

21811057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608159-G-A

21811135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608091-G-C

21811135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608091-G-T

21811267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608389-A-G

21811281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13608375-A-G

21811749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607479-G-T

21811769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607463-T-C

21812067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607198-C-T

http://identifiers.org/hco/16/GRCh38#21812093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13607171-C-A

21812093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607171-C-G

http://identifiers.org/hco/16/GRCh38#21812187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13607088-A-C

21812193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607082-C-G

21812232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607020-G-C

21812232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607020-G-T

21812243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607009-A-G

21812244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607008-A-G

21812251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13607001-A-G

21812273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606970-A-G

21812273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606970-A-T

http://identifiers.org/hco/16/GRCh38#21812292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13606945-C-A

21812293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606944-A-G

21812311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606926-G-A

21812311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606926-G-T

21812326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606911-G-A

21812405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606832-C-G

21812405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606832-C-T

http://identifiers.org/hco/16/GRCh38#21812446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13606791-A-C

21812470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606779-T-C

21812487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606762-T-G

21812491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606758-T-C

21812493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606756-C-T

21812494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606755-T-A

21812494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606755-T-C

21812494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606755-T-G

21812497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606752-A-G

http://identifiers.org/hco/16/GRCh38#21812508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13606741-A-C

21812508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606741-A-T

21812521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 13606730-C-G

http://identifiers.org/hco/16/GRCh38#21812524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13606727-A-C

21812524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13606727-A-G

21812533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606718-T-C

21812541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606710-T-C

21812562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606689-T-C

21812597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13606654-G-C

21812621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606628-A-G

21812621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13606628-A-T

21814754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604505-G-T

http://identifiers.org/hco/16/GRCh38#21814825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13604448-C-A

21814898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604389-A-G

21815004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604287-A-G

21815021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604268-G-T

21815049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604240-T-C

21815051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13604238-T-C

21817457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601996-A-G

21817478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13601975-A-G

21817478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13601975-A-T

21817530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601923-G-A

21817530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601923-G-T

21817549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601900-G-C

21817638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601814-T-A

21817682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601767-C-T

21817686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601763-T-A

21817773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601514-G-A

21817889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601431-T-C

21818150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601191-C-G

21818186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601159-T-C

21818245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601124-G-C

21818256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601113-G-T

21818283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601091-G-A

21818298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13601073-C-T

21818604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13600004-A-G

21818604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13600004-A-T

21818606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13600002-T-C

http://identifiers.org/hco/16/GRCh38#21818655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599961-C-A

21818655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 13599961-C-T

21818660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599956-T-C

21818660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599956-T-G

21818669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599947-A-G

21818717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599899-G-A

http://identifiers.org/hco/16/GRCh38#21818747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599869-C-A

21818747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599869-C-G

21818747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599869-C-T

21818814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599808-T-C

21818865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599759-G-C

21818865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599759-G-T

http://identifiers.org/hco/16/GRCh38#21818881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599743-C-A

21818881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599743-C-T

21818893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599728-T-C

http://identifiers.org/hco/16/GRCh38#21818894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599727-C-A

http://identifiers.org/hco/16/GRCh38#21819201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599444-C-A

21819201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599444-C-T

http://identifiers.org/hco/16/GRCh38#21819299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599423-C-A

21819299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599423-C-T

http://identifiers.org/hco/16/GRCh38#21819610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13599314-C-A

21819703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 13599220-C-G

21819703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 13599220-C-T

21819811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599134-A-G

21819868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599079-G-A

21819868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13599079-G-T

21819948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598976-G-T

21819988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598939-A-G

21820250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598746-G-A

21820250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598746-G-C

21820250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598746-G-T

http://identifiers.org/hco/16/GRCh38#21820280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#13598716-C-A

21820280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 13598716-C-T

21820282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598714-G-A

21820282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598714-G-C

21820282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598714-G-T

21820285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13598711-T-C

http://identifiers.org/hco/16/GRCh38#21820294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#13598702-C-A

21820294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 13598702-C-T

21820316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13598680-G-A

21820316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13598680-G-C

21820316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non coding transcript exon variant
orthologous variants: 13598680-G-T

21820337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598665-G-A

21820337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598665-G-C

http://identifiers.org/hco/16/GRCh38#21820351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#13598651-C-A

21820351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598651-C-G

21820351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598651-C-T

21820357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598645-A-G

21820362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598641-G-A

21820362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598641-G-C

21820362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598641-G-T

21820364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598639-G-A

21820364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598639-G-C

21820364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598639-G-T

http://identifiers.org/hco/16/GRCh38#21820370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#13598633-C-A

21820370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598633-C-G

21820370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598633-C-T

http://identifiers.org/hco/16/GRCh38#21820382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#13598621-C-A

21820382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30548
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 13598621-C-T