51662816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570517-C-T

51663133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570200-C-G

51663223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570110-C-G

51663223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570110-C-T

51663376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106569957-G-A

51663486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106569847-G-T

http://identifiers.org/hco/3/GRCh38#51663694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569655-C-A

51663751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569602-A-G

51663764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569590-C-G

51663764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569590-C-T

51663765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569589-T-C

51663772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569582-A-G

51663772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569582-A-T

http://identifiers.org/hco/3/GRCh38#51663817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569542-C-A

51663817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569542-C-G

51663817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569542-C-T

51664024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569322-G-A

51664024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569322-G-T

http://identifiers.org/hco/3/GRCh38#51664375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569013-C-A

51664375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569013-C-T

http://identifiers.org/hco/3/GRCh38#51664407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106568984-C-A

51664407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568984-C-T

51664705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568680-A-G

51664987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568383-C-T

http://identifiers.org/hco/3/GRCh38#51665060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106568302-A-C

51665060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568302-A-G

51665092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568265-T-C

51665161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568193-C-T

51665171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568183-G-C

51665171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568183-G-T

51665662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567733-G-T

51665695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567700-G-T

51665697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567698-A-G

http://identifiers.org/hco/3/GRCh38#51666016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106567377-C-A

51666022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567371-A-G

http://identifiers.org/hco/3/GRCh38#51666137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106567260-A-C

51666137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567260-A-G

51666164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567232-A-G

51666164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567232-A-T

51666265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567171-G-A

51666282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567154-G-A

51666282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567154-G-T

51666507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566955-G-C

http://identifiers.org/hco/3/GRCh38#51666540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566925-C-A

51666540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566925-C-G

51666567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566898-T-C

51666570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566895-G-A

51667045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566547-G-C

51667066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-A

51667066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-C

51667066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-T

51667161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566452-C-T

http://identifiers.org/hco/3/GRCh38#51667573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566345-C-A

http://identifiers.org/hco/3/GRCh38#51667602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566325-C-A

51667739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566204-T-A

51667814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566130-G-T

51667825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566119-G-A

http://identifiers.org/hco/3/GRCh38#51668233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106565717-C-A

51668334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106565608-G-T

51668387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106565555-G-T

51668747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106565204-G-T

51668752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106565199-G-T

51668758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106565193-G-T

51668776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106565182-A-G

51668933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106565031-C-T

51669242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106564791-G-A

51669270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106564762-C-G

51669854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106564312-G-A

51669854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106564312-G-T

51669935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106564239-G-A

51670277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106563997-A-T

51670391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106563906-T-C

51670782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563565-G-A

51671037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106563291-T-G

http://identifiers.org/hco/3/GRCh38#51671089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106563241-C-A

51671092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563238-G-T

51671093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563237-G-A

51671093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563237-G-T

51671114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563206-G-A

51671129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106563191-G-A

http://identifiers.org/hco/3/GRCh38#51671205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106563116-C-A

51671205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106563116-C-T

http://identifiers.org/hco/3/GRCh38#51671243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106563078-C-A

51671243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106563078-C-G

51671243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106563078-C-T

http://identifiers.org/hco/3/GRCh38#51671393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562956-C-A

51671393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562956-C-T

http://identifiers.org/hco/3/GRCh38#51671404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562945-C-A

51671404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562945-C-T

51671409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562940-C-T

51671465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, start_lost
orthologous variants: 106562885-A-G

http://identifiers.org/hco/3/GRCh38#51671501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562849-C-A

51671501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562849-C-T

http://identifiers.org/hco/3/GRCh38#51671502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562848-C-A

51671502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562848-C-T

51671504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562847-A-G

51671568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562783-T-C

51671568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562783-T-G

http://identifiers.org/hco/3/GRCh38#51671595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562760-C-A

51671595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562760-C-G

51671595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562760-C-T

51671599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562756-G-A

51671599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562756-G-T

http://identifiers.org/hco/3/GRCh38#51671606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562749-C-A

51671655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106562701-G-A

51671655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106562701-G-T

51671660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106562696-G-A

51671660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106562696-G-T

51671679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106562691-G-A

51671679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106562691-G-C

51671679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106562691-G-T

http://identifiers.org/hco/3/GRCh38#51671711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562683-C-A

51671726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562675-G-T

51671728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562673-T-A

51671728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562673-T-C

51671728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562673-T-G

51671835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562582-T-C

51671874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562547-G-A

51671877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562544-C-G

51671877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562544-C-T

51671884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562535-T-C

51671927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562493-G-T

51671974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106562446-C-T

51671996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562424-G-A

51671996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562424-G-T

http://identifiers.org/hco/3/GRCh38#51672080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562364-C-A

51672095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562351-G-T

51672097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562349-T-C

51672120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562317-G-T

51672153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562276-T-C

51672153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562276-T-G

51672176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562251-A-G

51672176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106562251-A-T

http://identifiers.org/hco/3/GRCh38#51672237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106562190-C-A

51672454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106561975-T-C

51672574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106561880-C-G

51672658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106561813-G-T

51672984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106561475-G-A

51673608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106560067-C-T

51673883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106559654-G-C

51674214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106559411-G-C

51674214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106559411-G-T

51674768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106558873-A-G

http://identifiers.org/hco/3/GRCh38#51674809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106558833-A-C

51675026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106558644-G-A

51675504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106558160-C-G

51675608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106558100-T-C

51676565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106557981-C-T

51676908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106557678-C-T

http://identifiers.org/hco/3/GRCh38#51677306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106557294-C-A

51677719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556870-T-C

51678066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556551-C-T

51678163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556449-C-T

51678185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556427-G-A

51678357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556256-G-A

51678530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106556116-A-G

51679279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106555325-A-G

51679618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106555030-G-T

51679916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554778-T-C

51679975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554723-G-A

http://identifiers.org/hco/3/GRCh38#51680271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106554565-C-A

51680356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554482-C-T

51680357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554481-G-A

51680358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554480-C-T

51680601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554247-C-T

51680619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554230-C-T

51680982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554025-C-T

51681000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106554006-C-T

http://identifiers.org/hco/3/GRCh38#51681019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106553987-A-C

51681019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106553987-A-G

51681070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106553941-G-A

51681295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106553749-G-A

51681295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106553749-G-T

http://identifiers.org/hco/3/GRCh38#51681415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106553637-C-A

51681415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106553637-C-T

51681454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106553597-A-G

51681650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106553410-T-C

51681662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106553398-G-T

51681689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106553371-T-C

http://identifiers.org/hco/3/GRCh38#51681744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106553320-A-C

51681744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106553320-A-T

51681936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106553182-A-G

51682027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106553099-A-G

51682063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106553063-G-T

http://identifiers.org/hco/3/GRCh38#51682236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106552890-C-A

51682257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552870-G-T

51682294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552833-T-A

51682294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552833-T-C

51682308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106552819-C-T

http://identifiers.org/hco/3/GRCh38#51682436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106552731-C-A

51682436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106552731-C-T

51682638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552555-A-G

51682833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552358-A-G

51682850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552344-G-T

51682867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552321-G-A

51682893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552296-T-C

51682899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552290-A-G

51682933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552257-G-C

51683039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552156-T-A

51683162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552082-T-C

51683172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106552072-A-G

51683268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551987-G-T

http://identifiers.org/hco/3/GRCh38#51683761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106551599-C-A

51683884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551471-T-G

51683889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551466-G-A

51683889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551466-G-T

51683939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551418-G-A

51683956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551402-T-G

51683976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551382-A-G

51683976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551382-A-T

http://identifiers.org/hco/3/GRCh38#51683987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106551372-C-A

51683987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551372-C-G

51683987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551372-C-T

51683988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551371-T-C

51684000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551359-C-T

51684093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551260-G-T

http://identifiers.org/hco/3/GRCh38#51684121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106551233-C-A

http://identifiers.org/hco/3/GRCh38#51684181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106551148-A-C

51684181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551148-A-G

51684182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551147-T-A

51684182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551147-T-G

51684190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551139-T-G

51684318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551033-T-C

51684325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551026-G-A

51684325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106551026-G-T

http://identifiers.org/hco/3/GRCh38#51684367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106550984-C-A

51684367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106550984-C-G

51684380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106550971-G-A

51684732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106550634-G-T

http://identifiers.org/hco/3/GRCh38#51684741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106550625-C-A

51684741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106550625-C-T

51685118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106550345-G-A

51686797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106549453-G-A

51687062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106549191-C-T

51687367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106549019-T-C

51687404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548983-G-A

51687436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548955-A-G

51687714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548676-G-A

51687821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548655-T-G

51687946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548539-T-C

51688012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548474-C-G

51688081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106548397-G-T

51688541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106547984-C-T

51690113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106547185-C-G

51690171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106547129-C-T

51690791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106546746-C-T

51691036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106546594-C-T

http://identifiers.org/hco/3/GRCh38#51691331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106546327-C-A

51691560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106546119-C-T

51692038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545673-C-T

51692207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545505-G-A

51692345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545380-C-G

51692453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545280-G-T

51692564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545185-T-C

51692601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106545150-C-T

51692974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544857-A-G

51693138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544694-C-T

http://identifiers.org/hco/3/GRCh38#51693322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106544511-C-A

51693342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544492-C-G

http://identifiers.org/hco/3/GRCh38#51693371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106544463-C-A

51694586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544175-T-A

51694586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544175-T-C

51694648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544112-A-G

51694690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106544073-C-T

51695338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106543384-T-C

51695339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106543383-T-G

51695385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106543344-G-A

51695882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106542916-T-C

51695882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106542916-T-G

51696029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106542788-A-G

51697150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106541781-A-G

51697308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106541618-C-T

51697482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106541464-G-A

51697618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106541317-C-T

51698054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540878-G-A

51698139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540796-G-A

51698236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540725-A-G

51698343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540618-C-T

51698478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540488-C-T

51698705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540285-T-C

51698861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106540169-C-T

http://identifiers.org/hco/3/GRCh38#51699305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106539822-C-A

51699307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539820-G-A

51699307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539820-G-C

51699343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539783-C-T

http://identifiers.org/hco/3/GRCh38#51699344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106539782-C-A

51699445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106539686-C-G

51699690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539437-A-G

51699704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539423-G-A

51699704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106539423-G-T

51700345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538960-T-G

51700792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538510-C-G

51700821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538485-C-T

51701022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538304-C-G

51701022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538304-C-T

51701172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538157-A-G

51701173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538156-G-A

51702328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106537715-T-C

51703381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536851-C-T

51703474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536756-A-G

51703540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536721-G-C

51703615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536646-G-C

51703653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536606-T-C

http://identifiers.org/hco/3/GRCh38#51703674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106536561-A-C

51703674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106536561-A-G

51704048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106536191-G-A

http://identifiers.org/hco/3/GRCh38#51704171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106536081-C-A

51704171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30247
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106536081-C-T