85752571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213698-A-G

85752764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213513-G-A

85752911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213413-T-C

85753197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213139-G-A

85753462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212922-T-G

85753575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212800-T-C

http://identifiers.org/hco/2/GRCh38#85753747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72212647-C-A

85753747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212647-C-G

85753747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212647-C-T

85753818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212576-G-A

85753818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212576-G-T

85753848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212546-G-A

85753848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212546-G-T

http://identifiers.org/hco/2/GRCh38#85753865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72212523-C-A

85753865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212523-C-T

85753866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212522-T-A

85753866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212522-T-C

http://identifiers.org/hco/2/GRCh38#85754016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72212369-A-C

85754042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212342-C-T

85754082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212302-A-G

85754082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212302-A-T

85754089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212293-G-A

85754089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212293-G-C

85754089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212293-G-T

85754147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212187-G-A

85754147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72212187-G-T

http://identifiers.org/hco/2/GRCh38#85754354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72211982-A-C

85754354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72211982-A-G

85754455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211875-G-A

85754455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211875-G-C

85754455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211875-G-T

85754496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211834-G-A

85754496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211834-G-C

85754496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72211834-G-T

85754617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72211719-A-G

85754658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72211678-T-C

85754797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72211536-A-G

85754797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72211536-A-T

85755068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211288-C-T

85755069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211287-C-G

85755069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211287-C-T

85755106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211265-C-G

85755106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211265-C-T

http://identifiers.org/hco/2/GRCh38#85755380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72210912-A-C

85755380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210912-A-G

85755474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210794-C-T

85755545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210726-T-G

85755802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210441-G-C

85756105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210179-C-G

85756105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210179-C-T

85756202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210116-C-G

85756202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210116-C-T

85756336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210012-G-A

85756429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209941-G-A

85756447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209923-T-C

85756447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209923-T-G

85756458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209910-G-A

85757062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72209470-A-G

85757065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72209467-C-G

85757138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209367-G-A

85757171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209334-T-C

85757180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209325-A-G

85757190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209315-C-T

85757845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208898-G-C

85758284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208523-C-T

85758330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208476-C-T

85758419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208394-C-G

85758428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208382-C-T

85758823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208023-C-T

85758824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208022-C-T

85758997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207843-G-T

85759054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207810-T-C

85759127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207740-G-A

85759206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207670-C-T

85760361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206309-C-G

85760361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206309-C-T

85760363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206307-G-A

85760627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206085-G-A

85760627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206085-G-T

85760668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72206045-A-G

85761038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205557-G-A

85761038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205557-G-T

http://identifiers.org/hco/2/GRCh38#85761039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72205556-C-A

85761039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205556-C-G

85761039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205556-C-T

85761213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205365-C-T

85761344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205219-A-G

85761351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205212-T-C

85761356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72205206-C-T

85761692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204911-C-T

85761703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72204905-C-T

http://identifiers.org/hco/2/GRCh38#85761778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72204845-C-A

85761852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72204783-G-A

85761852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72204783-G-C

85762567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202956-G-A

85762632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202891-G-A

85762792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202784-G-T

85762867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202681-C-T

85762946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202597-T-C

85762966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202577-T-C

http://identifiers.org/hco/2/GRCh38#85763162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72202399-C-A

85763468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202117-C-T

85763477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202108-T-G

85763594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201293-A-G

85763595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201292-C-T

85763901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201027-G-A

85763901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201027-G-C

85763901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72201027-G-T

85763947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200985-G-C

85763955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200956-G-A

85763955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200956-G-T

http://identifiers.org/hco/2/GRCh38#85764072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72200834-C-A

85764072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72200834-C-T

http://identifiers.org/hco/2/GRCh38#85764174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72200732-A-C

85764213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200694-T-C

85764367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200572-A-G

85764378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200561-C-T

85764389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200550-G-T

85764459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200484-A-T

85764682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72200268-T-C

85765070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199900-C-T

85765085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199885-G-A

85765338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199696-C-T

85765508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199552-C-T

http://identifiers.org/hco/2/GRCh38#85765676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72199358-C-A

http://identifiers.org/hco/2/GRCh38#85765678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72199356-A-C

85765702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199329-C-G

85765705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199326-G-A

85765705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199326-G-C

85765748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199293-G-T

85765754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199287-C-T

85765778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72199262-C-T

85767478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198616-A-T

85767480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198614-C-T

85768967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196696-G-C

85769004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196660-T-C

85769071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196599-G-T

85769082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196588-G-A

85769082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196588-G-C

85769123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196547-C-G

85769124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196546-C-T

85769281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196405-G-A

85769691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196024-G-A

85769710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196009-C-T

85769791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195922-C-T

85770402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195689-T-C

85770418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195673-A-G

85770446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195645-G-C

85770683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195404-T-C

85770765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195336-C-T

85771265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195006-C-T

85771314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194957-T-C

85771659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194653-G-A

85771772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194554-A-G

85771989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194363-C-T

85772115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194260-G-A

85772115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194260-G-T

85772320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194051-T-A

85772406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193963-C-T

85772811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72193560-T-A

85772952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72193398-A-T

85773195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192835-A-G

85773224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192805-T-C

85773317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192705-G-T

85773370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192652-G-A

85773370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192652-G-C

85773370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192652-G-T

http://identifiers.org/hco/2/GRCh38#85773399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72192623-C-A

85773399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192623-C-T

http://identifiers.org/hco/2/GRCh38#85773462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72192575-C-A

85773472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192566-G-A

85773472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192566-G-T

85773602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192438-A-G

85773604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192436-T-C

85773698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192348-G-A

85773747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192305-A-G

http://identifiers.org/hco/2/GRCh38#85773754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72192298-C-A

85773896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192169-A-G

85773934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192136-C-T

85773936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192134-G-T

85773939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192131-G-T

85773955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192125-G-T

85773956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192124-G-T

85773964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72192116-A-G

85775596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191635-G-T

85775811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191453-C-T

85775878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191386-C-T

85775931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191334-C-T

85775970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191296-T-G

85776054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191226-G-A

85776054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191226-G-T

85776282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191029-C-T

85776293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191018-G-A

85776319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190998-C-T

85776405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190906-G-A

85776420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190891-G-T

85777173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189922-C-T

http://identifiers.org/hco/2/GRCh38#85777476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72189683-C-A

85778378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189256-A-G

85778581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188717-C-T

85779266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188089-C-T

85779282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188073-C-T

85779357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188021-G-A

85779730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187486-C-T

85779991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187225-G-A

85780108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187121-C-G

85780108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187121-C-T

85780280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186993-C-T

85780482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186779-T-C

85780482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186779-T-G

85780524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186744-G-A

85780524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186744-G-T

http://identifiers.org/hco/2/GRCh38#85780528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72186740-C-A

85780528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186740-C-T

85780839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186460-A-G

85780839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186460-A-T

85780908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186413-A-G

85780971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72186350-G-T

85785130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185781-C-T

85785134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185777-A-T

85785229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185687-C-T

85786015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184907-C-T

85786331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184690-C-G

http://identifiers.org/hco/2/GRCh38#85786515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72184485-C-A

85786613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184371-C-T

85786792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184228-T-C

85786866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184152-G-A

85786866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184152-G-C

85786866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184152-G-T

85787321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183764-C-T

http://identifiers.org/hco/2/GRCh38#85787345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72183744-C-A

85787345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183744-C-T

http://identifiers.org/hco/2/GRCh38#85787389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72183702-C-A

85787389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183702-C-T

85787390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183701-T-C

85787390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183701-T-G

85787396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183695-T-C

http://identifiers.org/hco/2/GRCh38#85787397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72183694-C-A

85787398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183693-C-T

85787442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183645-T-C

85787442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183645-T-G

http://identifiers.org/hco/2/GRCh38#85787486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72183613-C-A

85787486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183613-C-T

85787488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183611-T-A

85787488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183611-T-C

85787488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183611-T-G

85787678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183422-T-C

85787888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183327-G-A

85787888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183327-G-T

85788126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183095-G-T

http://identifiers.org/hco/2/GRCh38#85788207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#72183063-C-A

85788207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72183063-C-G

85788533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24126
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72182755-C-T