16356260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24783160-T-A

16356260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24783160-T-C

16356292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24783192-A-G

16356292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24783192-A-T

16356391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783285-T-G

http://identifiers.org/hco/16/GRCh38#16357008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783789-A-C

http://identifiers.org/hco/16/GRCh38#16357043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783831-A-C

16357082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-G-C

16357082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-G-T

16357245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784091-C-T

http://identifiers.org/hco/16/GRCh38#16357410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784256-C-A

16357410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784256-C-T

16357419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784265-T-G

16357506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784352-T-A

http://identifiers.org/hco/16/GRCh38#16357516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784362-A-C

16357516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784362-A-G

http://identifiers.org/hco/16/GRCh38#16357631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784477-C-A

16357631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784477-C-T

16357659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-G-A

16357659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-G-T

16357715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784561-G-A

16357715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24784561-G-T

http://identifiers.org/hco/16/GRCh38#16357842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784685-C-A

16357842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784685-C-G

16358144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-G-A

16358144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-G-C

16358144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-G-T

http://identifiers.org/hco/16/GRCh38#16358163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784996-A-C

16358163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784996-A-G

16358163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784996-A-T

16358172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785006-G-A

16358172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785006-G-T

16358184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785020-G-A

16358184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785020-G-T

16358289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785113-A-G

16358310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785135-G-T

16358593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24786146-G-A

16358610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24786160-A-T

16358760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-A

16358760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-C

16358760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-T

16358888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786485-G-T

16358934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786547-T-C

16358941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786554-G-A

16359153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786810-C-G

16359153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786810-C-T

16359385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787133-C-T

16359980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24787623-G-A

16360026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24787654-C-T

16360056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24787684-G-A

16360195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24787823-C-T

16360652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788296-G-A

16360805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24788447-C-G

16360805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24788447-C-T

16361214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-G-A

16361214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-G-C

16361642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789369-C-T

16362166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789903-G-C

http://identifiers.org/hco/16/GRCh38#16362331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790148-C-A

16362331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790148-C-G

16362331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790148-C-T

16362453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24790271-G-T

http://identifiers.org/hco/16/GRCh38#16362679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790527-C-A

16362679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24790527-C-G

16362679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24790527-C-T

16362844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790707-T-G

http://identifiers.org/hco/16/GRCh38#16362899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790763-A-C

16362899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790763-A-G

16362899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790763-A-T

16362941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790790-G-A

16362941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790790-G-T

16363040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-G-A

16363040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-G-T

16363053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790890-T-C

16363053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790890-T-G

16363059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790896-G-A

16363059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790896-G-T

16363060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790897-G-A

16363060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790897-G-T

http://identifiers.org/hco/16/GRCh38#16363070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790907-A-C

16363070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790907-A-G

16363070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790907-A-T

http://identifiers.org/hco/16/GRCh38#16363071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790908-C-A

16363071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790908-C-T

16363077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-A

16363077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-C

16363077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-T

http://identifiers.org/hco/16/GRCh38#16363084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790921-C-A

16363084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-C-G

16363084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-C-T

16363146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790940-G-A

http://identifiers.org/hco/16/GRCh38#16363210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24791004-C-A

16363210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24791004-C-G

16363210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24791004-C-T

http://identifiers.org/hco/16/GRCh38#16363243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24791037-C-A

16363243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24791037-C-T

16363295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791089-G-A

16363295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791089-G-C

16363295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791089-G-T

http://identifiers.org/hco/16/GRCh38#16363379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24791159-C-A

16363379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791159-C-G

16363379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791159-C-T

16363450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791222-G-C

16364012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24791852-A-G

16364012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24791852-A-T

16364349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24792189-G-A

http://identifiers.org/hco/16/GRCh38#16364507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24792347-C-A

16364507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24792347-C-T

http://identifiers.org/hco/16/GRCh38#16364545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24792385-C-A

16364884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24792724-C-T

http://identifiers.org/hco/16/GRCh38#16364968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24792808-C-A

16364968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24792808-C-T

http://identifiers.org/hco/16/GRCh38#16365160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793000-C-A

16365160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793000-C-T

http://identifiers.org/hco/16/GRCh38#16365170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793010-C-A

16365176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793016-G-A

16365176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793016-G-T

16365255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793094-A-G

16365370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793209-T-C

16365370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793209-T-G

16365371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793210-G-A

16365371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793210-G-T

16365422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793267-G-A

16365422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793267-G-T

http://identifiers.org/hco/16/GRCh38#16365457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793305-C-A

16365457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793305-C-T

http://identifiers.org/hco/16/GRCh38#16365479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793330-C-A

16365479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793330-C-T

16365513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793364-G-A

16365533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793384-C-T

http://identifiers.org/hco/16/GRCh38#16365566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793417-C-A

16365566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793417-C-G

16365566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793417-C-T

16365689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793540-C-T

16365771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793622-A-G

16365866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793717-C-T

16365877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793728-G-A

16365877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793728-G-C

16365959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793810-G-A

16365959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793810-G-C

http://identifiers.org/hco/16/GRCh38#16366036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793884-C-A

16366036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793884-C-G

16366036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793884-C-T

16366049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24793897-G-T

16366172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794020-T-G

http://identifiers.org/hco/16/GRCh38#16366325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24794173-C-A

16366325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794173-C-T

16366356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794204-C-T

http://identifiers.org/hco/16/GRCh38#16366606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24794455-C-A

16366606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794455-C-T

16366609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794458-G-A

16366609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794458-G-C

16366609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794458-G-T

http://identifiers.org/hco/16/GRCh38#16366718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24794567-C-A

16366718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794567-C-T

16366719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794568-G-A

16366719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794568-G-T

http://identifiers.org/hco/16/GRCh38#16366990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24794839-C-A

16366990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794839-C-G

16366990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794839-C-T

16367092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794941-G-A

16367092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24794941-G-T

http://identifiers.org/hco/16/GRCh38#16367376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24795237-C-A

16367376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24795237-C-T

http://identifiers.org/hco/16/GRCh38#16367410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24795267-C-A

16367410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795267-C-G

16367410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795267-C-T

16368020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795954-G-A

16368020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795954-G-T

16368154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796091-G-A

16368182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796126-C-G

http://identifiers.org/hco/16/GRCh38#16368314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796217-A-C

16368337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796240-G-A

16368426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796310-C-T

16368456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796336-C-T

http://identifiers.org/hco/16/GRCh38#16368800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796621-C-A

16368800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24796621-C-T

16368919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796691-C-T

16368999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24796780-A-G

http://identifiers.org/hco/16/GRCh38#16369123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796904-C-A

16369123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24796904-C-T

http://identifiers.org/hco/16/GRCh38#16369358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797112-C-A

16369358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797112-C-G

16369358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797112-C-T

16369422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797176-C-G

16369422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797176-C-T

16369519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-A

16369519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-T

16369565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797321-C-G

16369565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797321-C-T

http://identifiers.org/hco/16/GRCh38#16369582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797338-C-A

16369582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-C-G

16369582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-C-T

16369592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24797349-G-A

16369592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24797349-G-C

16369592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24797349-G-T

16369662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797419-G-A

16369662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797419-G-C

http://identifiers.org/hco/16/GRCh38#16369915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797633-A-C

16370182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797818-C-G

16370182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24797818-C-T

16370374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797999-G-A

http://identifiers.org/hco/16/GRCh38#16370956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798859-C-A

16370956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798859-C-T

http://identifiers.org/hco/16/GRCh38#16370987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798888-C-A

16370987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798888-C-T

16371051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798942-C-G

16371051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798942-C-T

16371087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798978-A-G

16371099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798990-C-G

16371099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798990-C-T

16371105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798996-A-G

16371105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24798996-A-T

http://identifiers.org/hco/16/GRCh38#16371157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24799048-C-A

16371157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-C-G

16371157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-C-T

16371547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799438-G-A

16371547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799438-G-C

16371547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799438-G-T

16371574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799465-G-A

16371574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799465-G-C

16371574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24799465-G-T

16371792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799683-G-A

16371792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799683-G-C

16371792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799683-G-T

16371854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799768-G-A

16371854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799768-G-C

16371890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799788-G-T

http://identifiers.org/hco/16/GRCh38#16372163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24800070-C-A

16372163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-C-T

16372275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-T-G

http://identifiers.org/hco/16/GRCh38#16372470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24800348-C-A

16372470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24800348-C-T

16372491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24800369-C-T

16372618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800487-A-G

16372655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800528-T-A

16372655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800528-T-C

16372869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-G-A

16373312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801158-C-T

http://identifiers.org/hco/16/GRCh38#16373540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24801356-C-A

16373639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801444-C-T

http://identifiers.org/hco/16/GRCh38#16373709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24801505-C-A

16373709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801505-C-G

16373709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801505-C-T

16373776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801622-G-A

16374352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24804652-T-C

http://identifiers.org/hco/16/GRCh38#16374355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24804655-C-A

http://identifiers.org/hco/16/GRCh38#16374457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24804757-C-A

16374457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24804757-C-T

16374472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-G-A

16374472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-G-T

16374528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24804828-G-A

http://identifiers.org/hco/16/GRCh38#16374532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24804843-A-C

16374532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804843-A-G

16374633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24804922-G-A

http://identifiers.org/hco/16/GRCh38#16374754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805043-A-C

16374754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805043-A-G

16374760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805049-T-A

16374806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805091-C-T

16374811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805096-T-C

16374855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24805147-C-G

16375153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24805442-G-A

16375153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non coding transcript exon variant
orthologous variants: 24805442-G-T

16376942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30066
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24806155-G-T