77310925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21496006-T-G

77311119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495830-T-C

http://identifiers.org/hco/7/GRCh38#77311204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495756-C-A

77311230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495730-C-T

77311326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495647-T-G

http://identifiers.org/hco/7/GRCh38#77311340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495643-C-A

77311340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495643-C-G

77311340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495643-C-T

77311374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495609-A-G

77311413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 21495570-G-A

http://identifiers.org/hco/7/GRCh38#77311442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495541-A-C

http://identifiers.org/hco/7/GRCh38#77311445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495538-C-A

77311445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21495538-C-T

77311466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495517-A-G

77311486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495452-T-C

77311503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495436-A-G

77311506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495433-T-C

77311639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495325-T-C

77311649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495315-T-A

77311684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495283-T-C

http://identifiers.org/hco/7/GRCh38#77311722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495248-C-A

77311786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495186-G-T

77311789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495183-T-C

http://identifiers.org/hco/7/GRCh38#77311858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21495123-A-C

77311858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495123-A-G

77311858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495123-A-T

77311894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495087-A-G

77311894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21495087-A-T

77312052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21494932-A-G

77312114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21494873-T-C

77312234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494755-T-A

77312319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494666-G-A

77312319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494666-G-T

77312343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494642-G-T

77312526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494466-G-A

77313033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494050-C-T

77313073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21494010-C-T

77313184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493905-C-T

77313294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493799-G-A

77313318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493777-G-T

77313400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493723-A-T

77313401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493722-A-G

77313436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493690-A-G

77313438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493688-G-T

77313533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21493600-C-T

http://identifiers.org/hco/7/GRCh38#77313670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21493464-C-A

77313670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493464-C-G

77313921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493218-T-C

77313923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21493216-G-T

77314135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492999-T-C

77314178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492970-A-G

77314267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-A

77314267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-C

77314267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492883-T-G

http://identifiers.org/hco/7/GRCh38#77314272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492878-C-A

77314272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492878-C-T

77314301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21492860-C-T

77314432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492730-A-G

77314520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492640-G-T

77314542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492618-C-T

77314559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492602-G-T

77314580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492577-A-G

77314595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492565-G-T

77314688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492530-T-A

77314695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492523-A-G

77314823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492488-G-C

77314876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492435-G-A

77314876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492435-G-T

http://identifiers.org/hco/7/GRCh38#77314892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492416-C-A

77314892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492416-C-T

http://identifiers.org/hco/7/GRCh38#77315001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21492318-A-C

77315002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492317-G-A

77315064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492244-A-G

77315177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492137-G-A

77315183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492131-G-A

77315201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492117-A-G

77315208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492110-A-G

77315241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21492087-A-G

77315361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491979-C-G

77315366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491974-G-T

77315455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491893-A-G

http://identifiers.org/hco/7/GRCh38#77315461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21491887-C-A

77315511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491847-G-T

77315611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491755-T-C

77315725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491629-G-C

77315928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491445-G-T

77316124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491245-T-G

77316183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491217-G-T

http://identifiers.org/hco/7/GRCh38#77316186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21491214-C-A

77316186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21491214-C-T

77316240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21488999-G-T

77316608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488650-C-G

77316711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488563-C-T

77316725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21488543-A-G

77319131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487870-A-G

77319152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487847-A-G

77319287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487723-T-C

77319421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487601-T-C

77319601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487423-A-T

77319785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487228-G-C

77319809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487204-T-G

77319913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487091-A-G

77319940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487065-G-A

77319940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21487065-G-T

77320181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486895-C-T

77320219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486859-T-C

77320584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486712-G-C

77320584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486712-G-T

77320652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486659-G-T

77320724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 21486599-C-T

77320935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486406-A-G

77320936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486405-T-G

http://identifiers.org/hco/7/GRCh38#77320958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21486383-A-C

77321263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486146-A-G

77321263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486146-A-T

77321264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486145-G-A

77321264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21486145-G-T

77321440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485955-T-G

http://identifiers.org/hco/7/GRCh38#77321473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21485923-C-A

77321496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485899-G-T

http://identifiers.org/hco/7/GRCh38#77321513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21485882-C-A

77321513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485882-C-T

77321947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485465-T-C

77322031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485368-G-A

77322108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485290-A-G

77322136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21485259-A-G

77322483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484988-G-A

77322527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21484947-G-A

77322984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483459-G-A

77323570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483210-T-A

77323570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483210-T-C

77323612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483173-A-G

77323612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483173-A-T

77323614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483171-G-A

77323614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483171-G-T

77323616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483169-G-A

77323616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483169-G-T

http://identifiers.org/hco/7/GRCh38#77323617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21483168-C-A

77323617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483168-C-T

77323631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483152-A-G

77323760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21483023-A-G

77323802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482981-T-C

77323811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482967-A-G

http://identifiers.org/hco/7/GRCh38#77323878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21482895-C-A

77323878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482895-C-T

77323880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21482893-T-C

77324107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479739-C-T

77324141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479705-A-T

77324168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479665-G-C

77324411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479363-T-G

http://identifiers.org/hco/7/GRCh38#77324496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21479262-A-C

77324496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479262-A-T

77324576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21479211-G-C

http://identifiers.org/hco/7/GRCh38#77326172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21478078-C-A

77326172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21478078-C-T

77326595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477895-A-G

77326595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477895-A-T

http://identifiers.org/hco/7/GRCh38#77326614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477877-A-C

77326724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477770-G-A

77326724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477770-G-T

77326830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477686-G-A

77326830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477686-G-T

77327070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477470-G-A

http://identifiers.org/hco/7/GRCh38#77327121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477421-C-A

77327121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477421-C-G

77327121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477421-C-T

77327170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477381-C-G

77327170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477381-C-T

77327180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477371-G-A

77327180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477371-G-T

77327205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477350-A-G

http://identifiers.org/hco/7/GRCh38#77327250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21477315-C-A

77327250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477315-C-T

77327411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21477229-T-C

77327809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476874-A-G

77328141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476674-T-C

77328142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21476673-T-C

77328172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476643-G-A

77328172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476643-G-T

http://identifiers.org/hco/7/GRCh38#77328306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476527-C-A

77328306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476527-C-T

http://identifiers.org/hco/7/GRCh38#77328373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476470-C-A

77328373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476470-C-T

77328382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476461-T-C

77328444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-A

77328444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-C

77328444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21476399-G-T

http://identifiers.org/hco/7/GRCh38#77328575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#21476271-C-A

77328628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 21476222-A-T

http://identifiers.org/hco/7/GRCh38#77329048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475809-C-A

77329264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21475646-A-G

77329360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475583-A-G

77329360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475583-A-T

http://identifiers.org/hco/7/GRCh38#77329405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475538-C-A

77329405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475538-C-G

77329405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475538-C-T

http://identifiers.org/hco/7/GRCh38#77329481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475455-C-A

77329481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475455-C-T

77329503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475437-T-G

77329650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475360-G-A

77329650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475360-G-C

77329695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475314-A-G

77329757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475255-G-A

77329757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475255-G-T

77329780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475230-A-G

77329780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475230-A-T

77329820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475203-T-C

77329821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475202-T-A

77329823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475200-G-A

77329823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475200-G-T

77329885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475172-T-A

77329885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475172-T-C

http://identifiers.org/hco/7/GRCh38#77329888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475169-A-C

77330066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475143-A-G

77330113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21475098-T-C

http://identifiers.org/hco/7/GRCh38#77330119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475092-A-C

http://identifiers.org/hco/7/GRCh38#77330261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21475004-C-A

http://identifiers.org/hco/7/GRCh38#77330372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21474893-A-C

http://identifiers.org/hco/7/GRCh38#77330469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21474784-C-A

77330469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474784-C-T

77330500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474751-A-T

77330516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474741-A-G

77330537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474727-T-A

77330625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474674-G-T

77330648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21474653-A-G

77330758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21474565-T-G

77330866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21474473-A-G

77330866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21474473-A-T

http://identifiers.org/hco/7/GRCh38#77331708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21470562-C-A

77331708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21470562-C-T

77331777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21470479-G-A

77331777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21470479-G-T

77331881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21470406-G-A

77331881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21470406-G-T

77332061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21470215-G-T

77332062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21470214-A-G

http://identifiers.org/hco/7/GRCh38#77332076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#21470201-C-A

77332076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21470201-C-T

77332706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21469199-T-A

77332809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21469111-A-T

77333446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468802-C-T

77333480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468776-C-T

77333524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468731-G-T

77333545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468714-G-C

77333545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468714-G-T

77333548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468711-T-G

77333793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468500-T-C

77333893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21468396-C-G

http://identifiers.org/hco/7/GRCh38#77335642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21467607-A-C

77335670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21467582-T-G

77335686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21467566-A-G

77335859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21467395-T-C

77335975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21467277-C-T

77335987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21467267-G-A

http://identifiers.org/hco/7/GRCh38#77336031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21467223-C-A

77337543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21466451-C-G

77337678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21466328-T-C

77337706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21466299-G-T

77337840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21465995-T-C

http://identifiers.org/hco/7/GRCh38#77338262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21465917-A-C

77338297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21465882-T-A

77338355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21465562-T-G

77338644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21465359-G-A

77348299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21464075-C-T

77348317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21464057-T-A

77348494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463897-C-T

77348647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21463765-C-T

77348667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463746-T-C

77348706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463703-T-A

77348958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463382-G-A

77349008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463234-A-G

77349115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463151-G-A

77349115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463151-G-C

77349168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463102-G-A

http://identifiers.org/hco/7/GRCh38#77349223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21463044-A-C

http://identifiers.org/hco/7/GRCh38#77349224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21463043-C-A

77349237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463031-C-G

77349240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463028-G-A

77349240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21463028-G-T

77349446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462840-T-G

http://identifiers.org/hco/7/GRCh38#77349458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21462827-A-C

77349459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462826-G-A

77349459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462826-G-C

77349459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462826-G-T

77351362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461084-C-G

77351383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461063-T-G

77351439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461025-A-G

http://identifiers.org/hco/7/GRCh38#77351583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21460900-A-C

77351583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460900-A-G

77351589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460894-G-A

77351589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460894-G-C

77351589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460894-G-T

77351657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21460828-C-T

77351856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460646-G-A

77351963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460541-G-A

77352003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460506-C-T

77352211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460024-G-T

77352452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459850-G-A

77352614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459711-C-T

77352713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459607-T-C

77352758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459565-A-T

77352831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459130-G-A

77352831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459130-G-C

77352831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459130-G-T

77352863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459098-G-A

77352863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459098-G-T

77352870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459091-G-T

77352874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459087-G-T

77353051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458945-G-A

77353051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458945-G-T

77353064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458932-G-A

77353122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458894-G-T

http://identifiers.org/hco/7/GRCh38#77353138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21458878-C-A

77353138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458878-C-T

http://identifiers.org/hco/7/GRCh38#77353150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21458868-A-C

77353150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458868-A-G

77353437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458578-G-C

77353437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458578-G-T

77353504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458502-A-T

77353529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21458478-A-G

77353622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21458385-T-C

77354084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457896-G-T

77354208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457765-T-C

77354374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457628-G-A

77354423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457551-C-G

77354425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457549-A-G

http://identifiers.org/hco/7/GRCh38#77354598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21457091-C-A

77354598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457091-C-T

77354699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457008-A-T

77354707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21457000-A-T

http://identifiers.org/hco/7/GRCh38#77354723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21456988-C-A

77354730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456981-G-T

77354743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456964-T-C

77355067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456281-G-A

77355067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456281-G-T

77355079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456269-G-A

77355079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456269-G-C

77355079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456269-G-T

77355115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456250-T-A

77355115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456250-T-G

77355120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456245-A-G

http://identifiers.org/hco/7/GRCh38#77355138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21456226-A-C

77355171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456193-G-A

77355171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456193-G-T

77355172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456192-T-C

77355177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456187-T-A

77355196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456169-A-G

77355208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21456157-C-G

77355246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21456119-G-A

http://identifiers.org/hco/7/GRCh38#77355287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21456078-A-C

77355287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21456078-A-T

77355305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21456060-G-A

77355327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21456038-G-A

77355557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 21455827-G-A

77355557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 21455827-G-C

77355557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 21455827-G-T

77356654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21455168-G-A

77356656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21455166-G-A

77356858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21455046-C-T

http://identifiers.org/hco/7/GRCh38#77356972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21454939-A-C

77357053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21454530-A-G

77357084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21454499-T-C

77359564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21453210-T-C

77359568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21453206-T-C

77359640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21453130-G-A

77360050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452808-C-T

77360335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452505-C-T

77360475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452379-T-A

77360610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452246-C-T

77360685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452191-G-A

77360685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452191-G-C

77360685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452191-G-T

77360688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452188-T-C

77360688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452188-T-G

http://identifiers.org/hco/7/GRCh38#77360699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21452178-C-A

77360699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452178-C-T

77360715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452163-A-G

77360747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452131-A-G

77360747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452131-A-T

77360809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452011-C-T

http://identifiers.org/hco/7/GRCh38#77360814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21452006-C-A

77360814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21452006-C-T

77360837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451983-A-G

77360842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21451978-T-C

77360843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451977-G-A

77360843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451977-G-T

http://identifiers.org/hco/7/GRCh38#77360846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21451974-C-A

77360846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21451974-C-G

77360846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451974-C-T

77360853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21451950-A-G

http://identifiers.org/hco/7/GRCh38#77360861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21451942-C-A

77360861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451942-C-G

77360861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21451942-C-T

77360907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21451889-A-G

77360908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21451888-A-G

http://identifiers.org/hco/7/GRCh38#77361019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21451794-C-A

77361512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449215-G-A

77361977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21448172-T-C

77362510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447956-T-G

77362519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447947-T-C

77362555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447907-A-G

77362556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447906-A-G

http://identifiers.org/hco/7/GRCh38#77362575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21447886-A-C

77362575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21447886-A-G

77362576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21447885-A-G

77362606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21447855-T-C

77362618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21447843-C-G

77362618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21447843-C-T

http://identifiers.org/hco/7/GRCh38#77362619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#21447842-C-A

77362619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21447842-C-T

77362639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21447822-C-T

77362662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21447799-T-C

77368738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438861-T-C

77369003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438596-G-A

77369250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438348-A-G

77369424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438183-T-G

77369539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21438079-T-A

77369698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21437931-T-C

77369902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436953-G-A

77369902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436953-G-T

77369933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436922-G-T

77370090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21436779-G-A

77373706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434712-T-G

77373935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434454-T-C

77374003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434340-C-T

77374039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434275-G-T

77374046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434268-T-A

77374046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434268-T-C

77374049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434265-A-G

http://identifiers.org/hco/7/GRCh38#77374098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21434214-C-A

77374105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21434207-T-C

77374118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21434194-C-G

77374160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21434152-G-A

77374160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21434152-G-T

http://identifiers.org/hco/7/GRCh38#77374200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21434111-A-C

77374200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434111-A-G

http://identifiers.org/hco/7/GRCh38#77374206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21434105-C-A

77374206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434105-C-T

http://identifiers.org/hco/7/GRCh38#77374258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21434058-C-A

http://identifiers.org/hco/7/GRCh38#77374265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21434051-C-A

77374265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21434051-C-T

77374502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433828-T-C

77374549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433784-T-G

77374629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433718-G-A

77374629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433718-G-T

http://identifiers.org/hco/7/GRCh38#77374658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21433687-A-C

77374671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433674-A-G

77374821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433526-G-T

77374891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433455-T-C

77374920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21433428-G-A

77375076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21433045-A-T

77375078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21433043-T-C

77375104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21433017-G-A

77375104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21433017-G-T

77375133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432669-A-G

77375133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432669-A-T

77375137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432665-A-G

http://identifiers.org/hco/7/GRCh38#77375164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21432639-C-A

77375164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432639-C-G

77375166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432637-G-A

http://identifiers.org/hco/7/GRCh38#77375203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21432612-C-A

77375203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432612-C-T

http://identifiers.org/hco/7/GRCh38#77375204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21432611-C-A

77375426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432406-T-C

77375460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432377-G-C

77375467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432369-T-C

77376200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432062-T-C

77376352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431988-C-T

77376405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431934-T-C

77376417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431922-C-T

http://identifiers.org/hco/7/GRCh38#77376843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431834-C-A

77376843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431834-C-G

77376843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431834-C-T

77376864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431813-T-C

http://identifiers.org/hco/7/GRCh38#77376942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431735-C-A

77376945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431732-G-A

77376945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431732-G-T

77377078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431590-G-A

77377104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431565-T-C

http://identifiers.org/hco/7/GRCh38#77377140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431532-C-A

77377140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431532-C-G

77377152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431520-G-A

77377152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431520-G-C

77377170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431502-T-G

http://identifiers.org/hco/7/GRCh38#77377183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431493-C-A

77377183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431493-C-T

77377199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431477-A-G

77377199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431477-A-T

77377206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431470-G-A

77377206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431470-G-C

77377206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431470-G-T

http://identifiers.org/hco/7/GRCh38#77377207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431469-A-C

http://identifiers.org/hco/7/GRCh38#77377216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431453-C-A

77377216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431453-C-T

http://identifiers.org/hco/7/GRCh38#77377224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431445-A-C

77377224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431445-A-G

77377237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431434-T-A

77377252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431419-A-G

77377262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431366-G-A

77377262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431366-G-T

http://identifiers.org/hco/7/GRCh38#77377267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431361-C-A

77377267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431361-C-T

http://identifiers.org/hco/7/GRCh38#77377271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431357-A-C

77377271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431357-A-T

77377293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431337-T-A

77377293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431337-T-C

77377293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431337-T-G

http://identifiers.org/hco/7/GRCh38#77377368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431262-A-C

77377368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431262-A-G

77377368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21431262-A-T

77377392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21431238-T-A

77377392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21431238-T-C

77377392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21431238-T-G

77377421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431218-A-G

77377421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431218-A-T

http://identifiers.org/hco/7/GRCh38#77377422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431217-A-C

77377422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431217-A-G

77377422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431217-A-T

77377541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431114-T-A

77377541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431114-T-C

77377543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431112-C-T

http://identifiers.org/hco/7/GRCh38#77377546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431109-A-C

http://identifiers.org/hco/7/GRCh38#77377629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21431041-A-C

77377712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430971-T-G

77377932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430788-C-G

77378076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430647-T-C

77378107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430619-C-T

http://identifiers.org/hco/7/GRCh38#77378773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21430173-C-A

77378773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430173-C-T

77378935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429646-C-T

77378967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429628-G-A

77379027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429568-C-T

77379249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429356-C-T

77379505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429160-G-C

77379797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428894-T-A

77379797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428894-T-C

77379894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21428832-A-G

77379925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21428801-T-C

77380006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428535-T-C

77380012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428529-A-G

77380049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428493-C-T

77380052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428490-T-C

77380053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428489-A-G

77380054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428488-C-T

77380157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428387-G-A

http://identifiers.org/hco/7/GRCh38#77380207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21428333-C-A

77380280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428296-T-G

77380514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428076-T-C

77380627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427944-G-A

77380762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427852-C-T

77380768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427846-T-C

77381013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427704-A-G

77381019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427698-C-T

77381036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427681-C-T

http://identifiers.org/hco/7/GRCh38#77381064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21427654-C-A

77381180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427550-T-A

77381180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427550-T-C

77381233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427497-T-C

77381241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427490-T-C

77381260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427471-G-A

77381260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427471-G-T

77381261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427470-G-A

77381261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427470-G-T

77381326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21427414-G-A

77381326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21427414-G-T

77381366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427367-A-G

http://identifiers.org/hco/7/GRCh38#77381375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21427358-A-C

77381375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427358-A-G

http://identifiers.org/hco/7/GRCh38#77381388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21427345-C-A

77381388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427345-C-T

http://identifiers.org/hco/7/GRCh38#77381395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21427338-A-C

77381395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427338-A-G

77381406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427324-T-A

77381406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427324-T-C

http://identifiers.org/hco/7/GRCh38#77381407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21427323-A-C

77381407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427323-A-G

77381407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427323-A-T

77381421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427309-A-G

77381629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427139-T-C

77381669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427112-A-G

77381675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427107-G-A

77381694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427089-G-A

77381694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427089-G-C

http://identifiers.org/hco/7/GRCh38#77381994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21426861-C-A

77382058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426813-C-G

77382149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426736-T-G

77382215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426670-G-A

77382405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426461-G-A

http://identifiers.org/hco/7/GRCh38#77382443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21426425-C-A

77382443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426425-C-T

http://identifiers.org/hco/7/GRCh38#77382459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21426409-C-A

77382508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426339-T-C

77382555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426310-C-T

http://identifiers.org/hco/7/GRCh38#77382731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21426134-C-A

77382731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426134-C-T

77382772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426093-G-C

77382772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426093-G-T

77382773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426092-A-G

http://identifiers.org/hco/7/GRCh38#77382779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21426086-C-A

77382779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426086-C-G

77382780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426085-T-A

77382781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426084-G-A

77382781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21426084-G-T

77382874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425996-A-G

77382875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425995-T-C

77383536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425673-G-A

77383845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425369-C-T

77384060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425173-T-G

77384070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425163-G-A

77384070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425163-G-C

77384070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425163-G-T

77384109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21425127-G-A

77384213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21424527-G-A

77384213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21424527-G-T

77384431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21424323-G-T

http://identifiers.org/hco/7/GRCh38#77385717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21423666-C-A

77385717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423666-C-T

77385842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423545-G-C

http://identifiers.org/hco/7/GRCh38#77385921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21423495-A-C

http://identifiers.org/hco/7/GRCh38#77385979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21423442-A-C

77385990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423431-T-G

77386710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423087-T-G

77386787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423018-G-A

77386787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21423018-G-C

77386826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422988-A-G

77387045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422788-G-A

77387045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422788-G-C

http://identifiers.org/hco/7/GRCh38#77387131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21422703-C-A

77387133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422701-T-A

77387173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422667-G-A

77387203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422638-C-T

77387230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422611-G-A

77387230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422611-G-T

77387270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422572-A-G

77387279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422559-A-G

77387289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422549-T-C

77387323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422511-A-G

77387324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422510-T-A

77387326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422508-A-T

77387354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422480-A-G

77387354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422480-A-T

77387369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21422465-A-G

77387369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21422465-A-T

77387414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21422420-G-A

77387414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21422420-G-T

77387464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422370-G-A

77387464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422370-G-T

77387480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422354-G-A

77387480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422354-G-C

77387480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422354-G-T

77387586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422214-T-C

77387600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422200-G-A

77387710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422079-G-A

77387714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422075-C-T

77387729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21422060-A-G

77387810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421999-A-G

77387883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421961-T-G

http://identifiers.org/hco/7/GRCh38#77387901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21421950-A-C

http://identifiers.org/hco/7/GRCh38#77387921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21421930-A-C

77388181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421628-C-T

77388264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421585-A-G

77388273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421576-G-A

77388320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421532-T-C

77388404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421451-A-G

77388452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421411-C-T

77388711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421196-G-C

77388711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21421196-G-T

77392953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21417187-C-T

77393360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416659-G-C

77393417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21416602-C-T

77393496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416525-G-C

77393535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416488-T-C

77393545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416478-C-G

http://identifiers.org/hco/7/GRCh38#77393557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21416466-C-A

77393563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416460-T-A

77393563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416460-T-C

77394488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415800-T-A

77394488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415800-T-C

77394522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415765-G-A

77394758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415484-C-G

77394907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415343-C-T

77395059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415187-T-C

77395276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414978-A-G

77395313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414946-C-T

77395322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414937-C-T

http://identifiers.org/hco/7/GRCh38#77395380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21414889-C-A

77395439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414834-A-G

77395615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414684-A-G

77395677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414632-C-T

77395789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414519-A-G

77396449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21413128-G-T

77396527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21413056-G-T

77396608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412978-A-G

77396955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412665-A-G

77396955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412665-A-T

77397029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21412590-C-G

http://identifiers.org/hco/7/GRCh38#77397084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21412536-C-A

77397084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412536-C-T

77397088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412533-T-C

77397132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412490-G-T

77397143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412480-G-A

77397143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412480-G-C

77397143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412480-G-T

http://identifiers.org/hco/7/GRCh38#77397150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21412473-A-C

77397150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412473-A-G

http://identifiers.org/hco/7/GRCh38#77397220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21412414-C-A

77397220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412414-C-T

77397331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412321-A-G

77397479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412183-T-C

77397667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21412006-T-A

77397814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411802-G-A

http://identifiers.org/hco/7/GRCh38#77397830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21411786-A-C

77397876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411728-G-A

77397881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411723-A-T

77398194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21411399-G-C

77399041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410336-T-C

77399240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410032-G-A

77399240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410032-G-T

77399265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409994-A-G

77399312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409945-T-G

77399314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409943-T-C

77399316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409941-C-T

77399436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409833-T-A

77399436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409833-T-G

77399468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21409808-C-T

77399515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21409766-T-C

77399805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409436-G-A

77399821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409420-G-A

77399821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409420-G-C

77400024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409235-G-C

77400218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409055-C-T

77400653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408677-T-C

http://identifiers.org/hco/7/GRCh38#77400965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21408044-C-A

77400965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408044-C-T

77400985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408030-A-G

77400985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408030-A-T

77400993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408023-G-A

77401038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407982-A-G

77401373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407664-G-A

http://identifiers.org/hco/7/GRCh38#77401620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21407392-C-A

77401639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407364-T-C

77401695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407302-T-C

77401738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407261-G-A

77401919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405772-G-A

77402021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21405671-T-A

77402776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404957-A-G

77402780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404953-G-T

77402833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21404896-T-C

77404477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401164-G-A

77404567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21401089-G-A

77404567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21401089-G-T

77404658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401002-G-A

77404658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401002-G-C

77404658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401002-G-T

77404772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400908-T-G

77404808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400873-G-A

77404808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400873-G-C

77404811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400870-T-C

http://identifiers.org/hco/7/GRCh38#77405953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21399556-C-A

77405953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399556-C-T

http://identifiers.org/hco/7/GRCh38#77405983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21399527-C-A

77406055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21399446-T-A

77406055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21399446-T-C

77406055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21399446-T-G

77406060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21399441-T-C

77406120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399382-G-A

77406120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399382-G-C

77406120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399382-G-T

77406226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399273-A-G

77406397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399092-C-T

77406455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399037-T-C

77407965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396358-A-G

77407993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396333-A-G

77408059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396272-A-G

http://identifiers.org/hco/7/GRCh38#77408142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21396200-A-C

77408325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396018-G-A

77408363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395976-T-C

77408737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395907-G-A

77408737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395907-G-T

http://identifiers.org/hco/7/GRCh38#77408754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21395896-C-A

77408754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395896-C-T

77408783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395858-T-C

77408897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395741-G-A

77408897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395741-G-T

77408919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395720-A-G

77409085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395574-C-T

http://identifiers.org/hco/7/GRCh38#77409413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21395417-C-A

77409413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395417-C-T

77409800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21395048-G-A

77409800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21395048-G-C

77409800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21395048-G-T

77409995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394774-G-A

77409995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394774-G-C

77410359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394319-C-T

77410372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394306-A-G

77410691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393992-A-T

77411023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393672-G-A

77411023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393672-G-C

77413783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392619-C-T

77415446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392226-T-G

77415448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392224-C-T

77415449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392223-C-T

77415477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392195-A-G

77415479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21392193-G-T

77415547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21392106-A-T

http://identifiers.org/hco/7/GRCh38#77415558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21392095-C-A

77415567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21392082-A-G

77415569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21392080-C-T

http://identifiers.org/hco/7/GRCh38#77415597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391993-C-A

77415597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21391993-C-G

77415597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21391993-C-T

http://identifiers.org/hco/7/GRCh38#77415652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391940-C-A

77415652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21391940-C-T

http://identifiers.org/hco/7/GRCh38#77415655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391937-C-A

77416122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391557-C-G

77416122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391557-C-T

http://identifiers.org/hco/7/GRCh38#77416135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391545-C-A

77416135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391545-C-T

77416168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391503-T-A

77416168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391503-T-C

http://identifiers.org/hco/7/GRCh38#77416170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391501-C-A

77416170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391501-C-T

http://identifiers.org/hco/7/GRCh38#77416177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391494-C-A

77416177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391494-C-G

77416177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391494-C-T

http://identifiers.org/hco/7/GRCh38#77416189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391479-C-A

77416189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391479-C-T

http://identifiers.org/hco/7/GRCh38#77416203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391465-C-A

77416203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391465-C-T

77416215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 21391453-G-A

77416215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 21391453-G-C

77416215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 21391453-G-T

77416217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 21391451-G-A

77416217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 21391451-G-C

77416217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 21391451-G-T

http://identifiers.org/hco/7/GRCh38#77416218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#21391450-C-A

77416218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391450-C-T

77416242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391438-T-A

77416242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391438-T-C

77416376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391327-G-A

77416506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21391201-G-A

77416533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391166-G-A

77416539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391160-G-C

77416588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21391122-C-T

77416591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21391119-G-C