52345837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496824-G-C

52345837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496824-G-T

52345857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496804-G-T

52345884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496777-G-T

http://identifiers.org/hco/1/GRCh38#52345889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108496772-A-C

52345946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496722-G-A

52345946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496722-G-T

http://identifiers.org/hco/1/GRCh38#52345953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108496715-C-A

52345953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496715-C-T

52345971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108496700-T-C

52346545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108496141-A-T

52347386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108495404-T-C

52348499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108494840-C-T

52349138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108494253-A-G

52349194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108494206-G-C

52349218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108494187-C-G

52349368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108494032-C-T

52349680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493648-T-C

52349782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493536-G-A

52349888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493464-T-G

52349941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493440-G-A

52349941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493440-G-C

52349941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108493440-G-T

52350701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492875-G-A

http://identifiers.org/hco/1/GRCh38#52350800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108492801-C-A

52350800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492801-C-T

52351157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492537-T-C

52351226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492466-A-G

52351237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492455-T-C

52351244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492448-G-C

http://identifiers.org/hco/1/GRCh38#52351367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108492371-C-A

52351400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492362-G-A

52351470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492300-A-G

52351471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492299-G-A

52351471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492299-G-T

52351472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492298-G-A

52351569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492217-G-T

52351604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492182-A-G

52351659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108492087-G-A

52351978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108491738-C-T

52351989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108491706-A-G

http://identifiers.org/hco/1/GRCh38#52352019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108491659-C-A

52352106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108491562-T-C

52352673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491178-T-C

52352674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491177-A-G

52352753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491103-A-G

52352753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491103-A-T

52352761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491095-A-G

http://identifiers.org/hco/1/GRCh38#52352766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108491090-C-A

52352766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108491090-C-T

52352897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490962-G-T

52352914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490945-C-T

52352940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490927-C-T

http://identifiers.org/hco/1/GRCh38#52352972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490896-C-A

52352972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490896-C-T

52353038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490862-T-C

52353038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490862-T-G

52353049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490851-A-G

52353114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490799-G-A

52353114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490799-G-T

52353177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490737-C-T

http://identifiers.org/hco/1/GRCh38#52353328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490658-C-A

52353328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490658-C-G

52353328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490658-C-T

http://identifiers.org/hco/1/GRCh38#52353329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490657-C-A

52353343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490643-T-C

52353347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490639-C-T

52353520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 108490493-C-T

52353535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108490478-T-G

http://identifiers.org/hco/1/GRCh38#52353622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490391-C-A

52353622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108490391-C-G

52353622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108490391-C-T

52353643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108490370-A-G

52353649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 108490364-T-C

52353688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490325-A-T

52353743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490293-A-T

52353781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490269-G-A

52353781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108490269-G-T

http://identifiers.org/hco/1/GRCh38#52353860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490194-A-C

http://identifiers.org/hco/1/GRCh38#52353897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490131-C-A

52353897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108490131-C-T

http://identifiers.org/hco/1/GRCh38#52353907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108490121-A-C

52353907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108490121-A-G

52353907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108490121-A-T

52353942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108490101-G-A

52353942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108490101-G-T

52354245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489884-T-A

52354245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489884-T-C

52354245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489884-T-G

52354281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489845-C-T

52354295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489831-T-C

52354442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108489236-T-C

52354466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489211-G-A

52354466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108489211-G-T

52355021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108488717-G-A

52355037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108488702-T-C

52355037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108488702-T-G

52355110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108488630-T-A

52355133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108488622-G-A

52355294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487890-G-A

52355294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487890-G-T

52355299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487885-G-A

52355299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487885-G-T

52355372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487818-G-A

52355385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487805-G-A

52355385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487805-G-C

52355455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 108487732-C-T

52355677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487462-G-A

52355677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487462-G-C

http://identifiers.org/hco/1/GRCh38#52356073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108487136-C-A

52356073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487136-C-G

52356073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487136-C-T

52356108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108487110-G-A

52356359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486851-G-A

52356494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486719-G-C

52356494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486719-G-T

52356528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486682-A-G

http://identifiers.org/hco/1/GRCh38#52356537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108486672-C-A

52356537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486672-C-G

http://identifiers.org/hco/1/GRCh38#52356548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108486661-C-A

http://identifiers.org/hco/1/GRCh38#52356551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108486658-C-A

52356551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486658-C-G

http://identifiers.org/hco/1/GRCh38#52356560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108486635-C-A

52356560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486635-C-G

52356560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108486635-C-T

http://identifiers.org/hco/1/GRCh38#52356687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108486363-A-C

52356687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486363-A-G

52356734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486283-T-C

52356829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486058-A-G

52356834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486053-T-G

52356886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486001-G-A

52356886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108486001-G-T

52356891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485996-T-C

http://identifiers.org/hco/1/GRCh38#52356968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485936-C-A

52356968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485936-C-T

52356983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485921-G-A

http://identifiers.org/hco/1/GRCh38#52357001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485903-C-A

52357047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485857-T-C

52357047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485857-T-G

http://identifiers.org/hco/1/GRCh38#52357108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485796-C-A

http://identifiers.org/hco/1/GRCh38#52357154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485750-C-A

52357154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108485750-C-T

52357168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108485736-T-G

52357210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485694-G-A

52357298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485616-T-C

52357395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485520-T-G

http://identifiers.org/hco/1/GRCh38#52357416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485501-C-A

52357488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485435-G-A

52357488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485435-G-T

http://identifiers.org/hco/1/GRCh38#52357489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485434-C-A

52357489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485434-C-T

http://identifiers.org/hco/1/GRCh38#52357490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108485433-C-A

52357536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485387-T-C

52357575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485348-T-C

52357611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485312-T-G

52357638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485285-T-A

52357638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485285-T-C

52357744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108485180-G-C

52357795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108485129-G-A

http://identifiers.org/hco/1/GRCh38#52357983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108484950-C-A

52357983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108484950-C-T

52358032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108484901-G-A

52358121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108484823-T-C

52358121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108484823-T-G

52358409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108484541-T-C

52358428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108484522-A-G

http://identifiers.org/hco/1/GRCh38#52358473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108484478-A-C

52358524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484427-G-A

52358568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484404-G-T

52358592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484380-G-T

52358737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108484264-C-T

http://identifiers.org/hco/1/GRCh38#52358870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108484141-C-A

52358928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484091-G-T

52358955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484068-G-A

52358955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484068-G-T

http://identifiers.org/hco/1/GRCh38#52358995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108484032-C-A

52358995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108484032-C-T

52359068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108483958-C-T

52359101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108483925-A-G

52359120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108483906-C-T

52359170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483855-A-G

52359192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483837-C-G

52359254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108483781-G-C

52359636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483403-A-G

52359648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483392-G-A

52359653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483387-T-C

http://identifiers.org/hco/1/GRCh38#52359665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108483375-C-A

52360004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483061-G-A

52360008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483057-G-C

52360008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483057-G-T

52360010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483055-T-G

52360039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108483039-A-G

52360133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108482950-T-C

52360196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108482887-C-T

52360253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108482829-C-T

http://identifiers.org/hco/1/GRCh38#52360317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108482781-A-C

52360351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108482756-C-T

52360484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108482668-C-T

52360752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108482399-G-T

52360921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108482254-C-G

52360921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108482254-C-T

52360922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108482253-G-A

52360922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108482253-G-C

http://identifiers.org/hco/1/GRCh38#52361376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108481840-C-A

52361376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481840-C-T

52361414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481810-G-A

52361414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481810-G-T

52361420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481804-A-G

52361526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108481729-T-C

52361645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481612-C-T

52361651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481606-T-G

52361731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481518-G-A

52361731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481518-G-T

52362003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481320-C-T

52362049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481277-G-A

52362084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481237-A-G

52362084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481237-A-T

52362243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481120-G-T

52362292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108481073-C-G

http://identifiers.org/hco/1/GRCh38#52362372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108480990-C-A

52362372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108480990-C-G

52362635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108480757-T-G

52364541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108478799-A-G

http://identifiers.org/hco/1/GRCh38#52364699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#108478637-C-A

52364777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108478582-A-G

52364899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108478373-G-A

52364912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108478355-T-C

52365920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477434-A-G

http://identifiers.org/hco/1/GRCh38#52365962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#108477391-C-A

52365962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477391-C-T

http://identifiers.org/hco/1/GRCh38#52365968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#108477385-C-A

52365968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477385-C-G

52365985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477350-G-A

52365985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477350-G-T

52366004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108477331-G-A

52366004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108477331-G-T

http://identifiers.org/hco/1/GRCh38#52366020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#108477316-C-A

52366020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477316-C-T

52366180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477149-G-A

52366180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29386
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108477149-G-T