21013537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141592978-T-A

21013542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141592983-G-A

21013542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141592983-G-T

http://identifiers.org/hco/12/GRCh38#21013582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141593024-C-A

21013595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593037-C-T

21013646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593105-G-C

21013662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593115-C-T

21013668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593121-C-G

21013668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593121-C-T

21013810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593278-G-T

http://identifiers.org/hco/12/GRCh38#21013983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141593900-C-A

21013983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593900-C-G

21013984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141593901-C-G

http://identifiers.org/hco/12/GRCh38#21015558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141594129-C-A

21015656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141594232-G-A

21015656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141594232-G-T

21015798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594372-A-G

21015798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594372-A-T

21015862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594418-G-A

21015862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594418-G-C

21015862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594418-G-T

http://identifiers.org/hco/12/GRCh38#21015867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141594423-A-C

21015971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594504-G-C

21016048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594552-G-A

21016119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594620-C-G

21016119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594620-C-T

21016164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594657-C-T

21016433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141594925-C-T

21018651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596591-C-T

21018688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596623-T-A

21018726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596661-C-G

21018782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596720-T-G

21018785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596723-T-A

21018785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596723-T-C

21018816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596762-G-A

21018851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141596799-C-T

21019085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598034-T-C

21019103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598052-G-A

21019103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598052-G-C

21019103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598052-G-T

http://identifiers.org/hco/12/GRCh38#21019114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141598064-C-A

21019114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598064-C-T

21019124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598074-T-A

21019124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598074-T-G

21019145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598083-G-T

http://identifiers.org/hco/12/GRCh38#21019147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141598085-A-C

21019147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141598085-A-G

21019317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141598238-T-C

21019357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141598278-T-A

21019357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141598278-T-C

http://identifiers.org/hco/12/GRCh38#21021141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141600744-C-A

21021165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600769-A-G

21021290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600871-C-T

http://identifiers.org/hco/12/GRCh38#21021323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141600906-C-A

21021323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600906-C-T

21021378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600951-G-A

21021378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600951-G-C

21021378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600951-G-T

21021400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600971-T-A

21021400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141600971-T-G

21021599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601161-A-G

21021599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601161-A-T

21021610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601171-G-A

21021610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601171-G-T

21021639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601209-A-G

21021660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601225-A-T

http://identifiers.org/hco/12/GRCh38#21021719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141601278-C-A

21022148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601630-T-C

21022155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601637-T-C

21022225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601686-G-A

21022289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601750-T-C

21022292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141601754-A-G

21022583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602206-G-A

21022774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602425-G-T

21022787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602448-T-A

http://identifiers.org/hco/12/GRCh38#21022801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141602458-A-C

21022801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602458-A-G

21022831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602496-C-G

21022833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141602498-C-T

21023320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141603364-T-C

21023381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141603425-T-G

21023500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141603555-T-C

21023507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141603562-C-T

21023875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141604760-T-G

21024081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605020-C-T

21024185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605129-C-T

21024335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605232-T-C

21024347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605242-T-A

21024348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605243-A-T

21024744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605838-A-G

21024876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605949-A-G

21024915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605986-G-A

21024915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141605986-G-C

http://identifiers.org/hco/12/GRCh38#21043184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141609165-C-A

http://identifiers.org/hco/12/GRCh38#21043186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141609167-A-C

http://identifiers.org/hco/12/GRCh38#21043270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141609250-A-C

21043270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609250-A-G

21043347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609317-A-G

21043387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609357-G-T

21043452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609422-T-C

21043477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609447-A-G

21043483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609453-T-C

21043536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609506-T-C

21043553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609523-A-T

21043573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609543-A-G

21043573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141609543-A-T

http://identifiers.org/hco/12/GRCh38#21043589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141609559-C-A

21043589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609559-C-T

21043608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609576-G-A

21043608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609576-G-T

21043622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609590-T-C

21043622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609590-T-G

21043666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141609626-T-C

21043911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141612356-C-T

http://identifiers.org/hco/12/GRCh38#21043915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141612360-C-A

http://identifiers.org/hco/12/GRCh38#21044148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141612570-C-A

21044293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141612654-G-A

21044442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141612801-T-A

21044778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141613783-G-C

21044798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141613813-T-C

21046021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141614332-G-T

21046216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141614647-T-A

21046762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141614786-A-G

21046775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141614795-G-A

http://identifiers.org/hco/12/GRCh38#21046788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141614808-A-C

http://identifiers.org/hco/12/GRCh38#21046994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141614993-C-A

21047007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141615007-A-G

21047198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141615197-T-A

21047252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141615263-T-C

21047253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141615269-G-A

21047253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141615269-G-T

21048827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141616904-G-A

http://identifiers.org/hco/12/GRCh38#21048828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#141616905-C-A

21048828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141616905-C-T

21048837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141616914-T-C

21048847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141616924-T-C

21048945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617029-A-G

21048972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617055-G-A

21048972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617055-G-T

21049274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617373-C-T

21049347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617446-A-G

21049646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617676-G-A

21049646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617676-G-T

http://identifiers.org/hco/12/GRCh38#21051977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141617750-C-A

21051977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617750-C-G

21051977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617750-C-T

http://identifiers.org/hco/12/GRCh38#21051997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141617769-C-A

21051997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617769-C-T

21052044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617812-C-T

21052066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617834-T-G

http://identifiers.org/hco/12/GRCh38#21052073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141617841-A-C

21052073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617841-A-G

21052073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141617841-A-T

21052260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 141618038-T-C

21052277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618055-T-C

21052333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618108-A-G

21052333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618108-A-T

21052339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618114-T-C

21052347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618122-T-C

21052385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618163-A-G

21052407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618185-G-A

21052432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141618208-A-G

21052715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141620946-G-A

21052732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141620963-C-T

21052837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621062-C-T

21054009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621494-C-T

21054052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621535-G-A

21054081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621564-A-G

http://identifiers.org/hco/12/GRCh38#21054103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141621586-A-C

21054177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621661-G-A

21054324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621794-G-A

21054324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621794-G-T

21054351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621820-A-G

21054365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621834-G-T

21054379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621856-T-G

http://identifiers.org/hco/12/GRCh38#21054400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141621877-C-A

21054400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621877-C-G

21054400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621877-C-T

21054417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621894-A-G

21054432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621909-A-T

21054434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621911-T-C

21054434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141621911-T-G

http://identifiers.org/hco/12/GRCh38#21054601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141622076-A-C

21054601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141622076-A-G

21054902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141622645-A-G

21055097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141623546-A-G

21055251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141623691-C-G

21055331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141623778-G-T

21055369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141623812-G-A

21055417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141623860-T-A

21055603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624040-A-G

21055622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624056-A-T

21055654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624081-T-A

21055787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624186-C-T

21055921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624301-T-C

21065615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141624961-G-A

21065925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141625270-T-A

21065932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141625277-A-G

21065943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141625288-C-T

21066458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141625852-G-A

21066652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141626004-T-C

http://identifiers.org/hco/12/GRCh38#21066719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141626072-C-A

21066844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141626479-C-G

21066850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141626485-G-A

21066850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141626485-G-T

21067196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141626889-G-T

21067299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627016-T-C

21067441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627152-A-G

21067451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627163-A-T

21067469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627182-G-A

21067469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627182-G-C

21067469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627182-G-T

http://identifiers.org/hco/12/GRCh38#21067504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141627210-C-A

21067530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627234-A-G

21067642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627342-A-G

21067684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627371-A-G

21067885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141627532-A-T

http://identifiers.org/hco/12/GRCh38#21076397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141628875-C-A

21076397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141628875-C-T

21076424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141628902-A-G

21076448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141628926-G-A

21076547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141629025-A-G

21076547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141629025-A-T

http://identifiers.org/hco/12/GRCh38#21076614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#141629093-C-A

21076818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141629513-G-A

21076818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141629513-G-C

21076984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32934
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141629689-T-C