62433666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054161-T-A

62433666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054161-T-C

62433676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054153-A-G

62433676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054153-A-T

http://identifiers.org/hco/11/GRCh38#62433693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9054136-C-A

62433693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054136-C-G

62433693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054136-C-T

62433752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054077-A-T

http://identifiers.org/hco/11/GRCh38#62433756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9054073-A-C

62433756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9054073-A-T

62433939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053877-C-T

62433945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053871-A-G

http://identifiers.org/hco/11/GRCh38#62433975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9053856-C-A

62433975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053856-C-T

http://identifiers.org/hco/11/GRCh38#62433995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9053837-C-A

62433995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053837-C-T

http://identifiers.org/hco/11/GRCh38#62434014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9053812-A-C

62434041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053784-G-A

62434041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053784-G-T

62434116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053713-G-A

62434116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053713-G-C

62434140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053690-A-G

62434169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9053663-C-T

62439479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9052056-T-C

62440035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9051850-G-A

62440263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9051628-G-A

62440273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9051619-T-A

62440273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9051619-T-C

62440717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9051196-G-A

62440793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9051125-A-T

62444084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9049309-T-C

62444561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9048853-C-T

62444794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9048644-T-C

62444923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047940-G-T

62445102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047785-C-T

62445452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047515-G-C

62445454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047513-A-G

62445546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047421-G-A

http://identifiers.org/hco/11/GRCh38#62446116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9047332-C-A

62446217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047244-G-A

62446222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047239-G-C

62446430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9047054-G-A

62446529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046965-G-A

62446681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046828-T-A

62446740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046774-A-G

62446776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046754-G-A

62447055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046125-G-A

62447120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9046063-C-T

62447380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9045838-G-A

http://identifiers.org/hco/11/GRCh38#62448001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9045129-C-A

62448001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9045129-C-G

62448042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9045089-G-A

62448103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9045035-G-C

62448243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9044906-T-C

62448573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9044614-G-A

62448595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9044603-T-A

62448613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9044585-G-A

62449401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9043897-G-A

62449841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9043348-C-T

62453372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9041455-T-G

62456742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9039277-C-T

http://identifiers.org/hco/11/GRCh38#62458409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9038895-A-C

62458452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9038854-G-A

http://identifiers.org/hco/11/GRCh38#62458514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9038793-C-A

62458732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9038627-A-G

http://identifiers.org/hco/11/GRCh38#62459121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9038326-C-A

62461544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9037337-C-G

62461881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9037072-T-A

62461913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9037040-C-T

62462357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9036457-G-C

http://identifiers.org/hco/11/GRCh38#62463332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9034757-C-A

62463332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9034757-C-T

62463428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9034677-C-G

62463495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9034629-C-G

62463495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9034629-C-T

62463907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9034235-G-A

62467722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9033354-C-T

62467777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9033296-G-C

62477926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9028157-C-T

62478010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9028055-G-A

http://identifiers.org/hco/11/GRCh38#62478256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9027814-A-C

62479470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9025675-T-C

62479474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9025671-T-G

62479555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9025592-T-C

http://identifiers.org/hco/11/GRCh38#62479745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9025395-A-C

62480163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9024993-C-T

62480280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9024895-G-T

62480713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9024793-G-A

62480855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024649-C-G

62480882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024618-T-A

62481010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024499-T-C

62481066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9024458-T-C

62481708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9023324-G-A

62481845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9023158-G-A

62481922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9023128-T-C

http://identifiers.org/hco/11/GRCh38#62482898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9022939-C-A

62482898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9022939-C-T

62483149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9022501-A-T

62483192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9022458-A-G

62483340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9022314-G-T

62487863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9017012-G-C

http://identifiers.org/hco/11/GRCh38#62488032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9016828-C-A

http://identifiers.org/hco/11/GRCh38#62488358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9016536-A-C

62488800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9016417-G-A

62489287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9015977-G-T

62489324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9015936-C-T

62489680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9015590-G-A

62491574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014761-C-T

62491645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014727-G-A

62491645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014727-G-T

62491685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014666-A-T

62491867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014484-C-T

http://identifiers.org/hco/11/GRCh38#62491969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9014387-C-A

62491969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014387-C-T

62492054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9014336-G-A

62492330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9014094-T-G

62492442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9013987-T-C

62492527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9013904-G-A

62492527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9013904-G-T

62499594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9011632-T-C

62499657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9011588-G-A

62499712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9011550-A-G

62499753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9011509-T-C

62500209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9011110-C-T

62500640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9010683-G-A

62501892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9009953-C-T

http://identifiers.org/hco/11/GRCh38#62501980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9007931-A-C

62502062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007881-C-T

62502063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007880-C-T

62502417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007535-C-T

62502490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007460-G-A

62502490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007460-G-C

http://identifiers.org/hco/11/GRCh38#62502513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#9007437-A-C

62502764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9007175-C-T

62502998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9006984-T-C

62502999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9006983-G-T

62503053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9006157-T-G

62503146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9006073-C-T

62503276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9005955-C-T

62504441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9005467-C-T

62504632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9005273-G-C

62504743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9005148-T-G

62504748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9005139-G-A

62504748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9005139-G-T

62506667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9003360-T-A

62506706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9003342-G-A

62507060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9003028-G-A

62507060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9003028-G-T

62508132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9001177-C-T

62508697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9000641-C-T

62510541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998976-C-T

http://identifiers.org/hco/11/GRCh38#62510615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8998860-A-C

62510777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998646-A-G

62510796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998628-G-T

62510956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998563-A-G

62511012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998528-G-T

62511172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998377-A-G

62511202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998343-C-T

62511207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8998338-A-G

62513631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8997689-G-A

62513667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8997662-G-A

62513667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8997662-G-T

http://identifiers.org/hco/11/GRCh38#62515811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8996647-C-A

62515811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996647-C-G

62515818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996640-G-C

62515818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996640-G-T

62515828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996630-G-A

62515828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996630-G-T

http://identifiers.org/hco/11/GRCh38#62515866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8996592-A-C

62515866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8996592-A-G

62516044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8996418-G-T

62516150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8996314-C-T

62516260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8996204-G-A

62516833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 8995597-G-C

62517039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8995412-G-A

62517050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8995401-G-A

62517225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 8995226-G-C

62517807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8994644-G-T

http://identifiers.org/hco/11/GRCh38#62517935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8994537-C-A

62517935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8994537-C-T

http://identifiers.org/hco/11/GRCh38#62518167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8994305-C-A

62518167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8994305-C-G

http://identifiers.org/hco/11/GRCh38#62518339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8994133-C-A

62518379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8994093-T-A

62518440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8994032-G-A

http://identifiers.org/hco/11/GRCh38#62518445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8994027-C-A

62518591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8993881-G-C

62518649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8993823-A-G

62518770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8993702-C-T

62518979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8993493-T-C

62519409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8993063-G-A

62519532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992940-T-C

62519613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992853-G-A

62519613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992853-G-C

62519692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8992774-G-A

62519766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992700-T-A

62519766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992700-T-C

62519779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992687-C-T

62519809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992657-A-T

62519946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992520-T-G

62519955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992511-G-A

62519982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992484-G-A

http://identifiers.org/hco/11/GRCh38#62520009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8992457-C-A

62520009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992457-C-G

62520009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992457-C-T

62520031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992435-C-T

http://identifiers.org/hco/11/GRCh38#62520068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8992398-C-A

62520068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8992398-C-T

http://identifiers.org/hco/11/GRCh38#62520126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8992340-A-C

62520194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8992272-A-G

62520233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992233-T-A

62520240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992226-A-G

62520261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992205-G-A

62520338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8992128-A-G

62520338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8992128-A-T

62520408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992058-G-A

62520408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8992058-G-C

62520505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8991961-C-T

62520542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8991924-G-A

62520542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8991924-G-T

http://identifiers.org/hco/11/GRCh38#62520572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8991894-C-A

62520636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8991830-G-A

62520636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8991830-G-T

62521212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8991254-T-A

62521449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8991017-T-C

62521502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990964-T-A

62521502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990964-T-C

62521502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990964-T-G

62521510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990956-G-A

62521510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990956-G-C

62521513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990953-C-T

62521514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990952-A-G

62521539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990927-A-T

62521740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990726-A-G

http://identifiers.org/hco/11/GRCh38#62521787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8990679-C-A

62521890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990576-T-C

62522142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990330-G-A

http://identifiers.org/hco/11/GRCh38#62522166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8990306-A-C

62522166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990306-A-G

62522167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990305-A-G

62522167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990305-A-T

http://identifiers.org/hco/11/GRCh38#62522243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8990229-C-A

62522243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990229-C-G

62522243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8990229-C-T

62522319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990153-G-A

62522319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990153-G-T

62522379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990093-G-A

62522408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990064-C-G

62522421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990051-G-A

62522421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990051-G-C

62522457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8990015-G-A

62522477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989995-T-C

62522496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989976-T-A

62522539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989933-C-T

62522558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989914-A-G

62522612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989860-T-A

62522612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989860-T-C

62522612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989860-T-G

62522613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989859-A-G

62522622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989850-A-T

62522721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989751-T-C

62522733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989739-A-T

62522760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989712-T-C

62522766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989706-C-T

62522802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989676-T-G

62522955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989523-C-G

62522955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989523-C-T

62522994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989484-T-C

http://identifiers.org/hco/11/GRCh38#62522996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8989482-C-A

62522996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989482-C-G

62522996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989482-C-T

62523030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989448-T-A

62523030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989448-T-C

http://identifiers.org/hco/11/GRCh38#62523054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8989424-A-C

62523074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989404-G-A

62523074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989404-G-C

http://identifiers.org/hco/11/GRCh38#62523122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8989356-A-C

62523192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989286-G-A

62523192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989286-G-C

62523216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989262-T-A

62523225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989253-G-C

62523225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989253-G-T

62523228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989250-C-T

62523246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989232-G-A

62523296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8989020-G-A

62523296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8989020-G-C

62523342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988974-G-A

62523345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988971-A-G

62523408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988908-T-C

62523408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988908-T-G

62523468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988848-G-C

62523468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988848-G-T

62523486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988830-T-C

62523541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988775-G-A

62523558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988758-G-A

62523636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988680-T-C

http://identifiers.org/hco/11/GRCh38#62523644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8988672-C-A

62523644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8988672-C-G

62523651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988665-G-A

62523651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988665-G-T

62523652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988664-G-A

62523655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988661-C-T

62523657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988659-T-C

62523792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988524-T-A

62523792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988524-T-C

http://identifiers.org/hco/11/GRCh38#62523987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8988329-A-C

62523987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988329-A-G

62524118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988198-T-G

62524197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988119-A-G

62524272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8988044-C-T

62524443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987873-G-A

62524601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987715-T-A

62524601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987715-T-C

62524646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987670-G-A

62524719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987597-A-G

62524842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987474-T-A

62524842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987474-T-C

62524885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987431-C-T

62524897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987419-G-A

62524913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987403-T-A

http://identifiers.org/hco/11/GRCh38#62524923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8987393-C-A

62524923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987393-C-G

62524956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987360-T-C

62524958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987358-T-A

62524958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987358-T-C

62525049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987267-G-A

http://identifiers.org/hco/11/GRCh38#62525084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8987232-C-A

62525084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987232-C-G

http://identifiers.org/hco/11/GRCh38#62525123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8987193-A-C

62525187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987129-G-A

http://identifiers.org/hco/11/GRCh38#62525190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8987126-C-A

62525190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987126-C-T

62525241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987075-T-A

62525241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987075-T-C

http://identifiers.org/hco/11/GRCh38#62525288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8987028-A-C

62525288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8987028-A-G

62525288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987028-A-T

62525289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987027-T-A

62525298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987018-G-A

62525298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8987018-G-T

62525441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986875-G-C

62525451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986865-T-G

62525467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986849-A-G

62525479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986837-C-T

62525486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986830-C-T

62525532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986790-T-G

62525658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986664-T-A

62525665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986657-G-A

62525665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986657-G-C

62525760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986562-T-C

62525784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986538-A-G

62525804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986518-G-C

62525858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986464-C-G

62525858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986464-C-T

62525877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986445-G-A

62526039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986667-G-A

62526042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986664-T-G

62526049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986657-G-A

62526049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986657-G-C

62526144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986562-T-C

62526168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986538-A-G

62526168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986538-A-T

62526188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986518-G-C

62526237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986469-A-G

62526242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986464-C-T

62526252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986454-T-A

62526303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986403-G-A

62526306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986400-G-A

62526318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986388-A-G

62526338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986368-A-G

62526369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986337-A-G

62526416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986290-A-G

62526421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986285-C-T

62526431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986275-C-T

http://identifiers.org/hco/11/GRCh38#62526440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8986266-A-C

62526440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986266-A-G

62526440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986266-A-T

http://identifiers.org/hco/11/GRCh38#62526457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#8986249-C-A

62526494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986212-C-G

62526494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986212-C-T

62526495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986211-A-G

http://identifiers.org/hco/11/GRCh38#62526614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8986092-C-A

62526632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986074-G-A

62526632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8986074-G-T

62526642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986064-T-A

62526642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986064-T-C

62526645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986061-G-A

62526648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8986058-C-T

62526822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8985461-A-G

62527190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8985894-G-A

62527443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8985641-T-C

62527623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8985461-A-T

62527950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8985134-G-A

62528012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8985072-C-T

62528334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984126-G-A

http://identifiers.org/hco/11/GRCh38#62528384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8984076-C-A

62528535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984933-G-C

62528736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984732-G-A

62528736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984732-G-C

62528802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984666-T-A

62528802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984666-T-C

http://identifiers.org/hco/11/GRCh38#62529069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8984399-A-C

62529081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984387-G-A

62529342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984126-G-A

62529342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8984126-G-C

http://identifiers.org/hco/11/GRCh38#62529392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8984076-C-A

62529392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8984076-C-T

62529779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8983710-C-T

62529817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8983672-G-A

http://identifiers.org/hco/11/GRCh38#62530299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8983202-A-C

62530299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8983202-A-G

62530299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8983202-A-T

http://identifiers.org/hco/11/GRCh38#62530368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8983133-C-A

62530368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8983133-C-T

http://identifiers.org/hco/11/GRCh38#62530546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8982955-C-A

62530546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8982955-C-G

http://identifiers.org/hco/11/GRCh38#62530699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8982802-C-A

62530800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8982329-C-T

62530896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8982233-G-A

http://identifiers.org/hco/11/GRCh38#62531642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8981487-A-C

62532116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8981013-T-A

62532116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8981013-T-G

http://identifiers.org/hco/11/GRCh38#62532405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8980730-A-C

62532613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8980537-C-T

62532649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8980501-T-C

http://identifiers.org/hco/11/GRCh38#62532757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8980393-C-A

62533008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8980142-C-G

62533170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979980-T-C

http://identifiers.org/hco/11/GRCh38#62533259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8979891-C-A

62533458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979680-C-T

62533527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979611-T-C

62533572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979566-G-A

62533594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979544-C-T

62533693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979445-A-G

62533953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, missense_variant
orthologous variants: 8979182-C-T

http://identifiers.org/hco/11/GRCh38#62534091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8979044-C-A

62534091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8979044-C-G

62534091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8979044-C-T

http://identifiers.org/hco/11/GRCh38#62534126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8979009-C-A

62534126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8979009-C-T

http://identifiers.org/hco/11/GRCh38#62534156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8978978-A-C

http://identifiers.org/hco/11/GRCh38#62534162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8978972-C-A

62534162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978972-C-T

http://identifiers.org/hco/11/GRCh38#62534163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8978971-C-A

62534163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978971-C-G

62534163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978971-C-T

62534340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978816-G-C

62534592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978571-C-G

62534865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978346-A-G

62534893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978316-A-G

62534961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978268-C-T

62534983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978244-T-C

62534983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8978244-T-G

62535064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: missense variant
orthologous variants: 8978164-G-A

http://identifiers.org/hco/11/GRCh38#62535339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977895-C-A

http://identifiers.org/hco/11/GRCh38#62535762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977779-C-A

62535848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977699-C-T

62535867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977680-T-A

62535867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977680-T-C

62535932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977631-T-A

62535932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977631-T-C

62535977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: missense variant
orthologous variants: 8977586-G-C

62536007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: missense variant
orthologous variants: 8977556-C-T

62536267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8977302-A-G

http://identifiers.org/hco/11/GRCh38#62536278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977291-C-A

62536278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8977291-C-T

62536357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977240-G-A

62536357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977240-G-C

62536357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977240-G-T

http://identifiers.org/hco/11/GRCh38#62536400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977199-A-C

62536400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977199-A-T

http://identifiers.org/hco/11/GRCh38#62536421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977178-C-A

62536421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8977178-C-T

http://identifiers.org/hco/11/GRCh38#62536510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977093-C-A

62536510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5 prime UTR variant
orthologous variants: 8977093-C-T

http://identifiers.org/hco/11/GRCh38#62536542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8977051-C-A

http://identifiers.org/hco/11/GRCh38#62536683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8976913-C-A

62536683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8976913-C-T

62536691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8976905-G-A

62536691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8976905-G-T

62537991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8976563-G-A

62538540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8976048-C-T

62539126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8975404-G-A

62539322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8975222-C-T

62539335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8975209-T-C

62539382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8975163-C-T

62539549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8975006-G-A

62539734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8974838-T-A

62539734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8974838-T-C

62540201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8974475-C-G

62540773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8973337-A-G

62540954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8973157-C-T

62542123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8971121-A-G

http://identifiers.org/hco/11/GRCh38#62542198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8971026-C-A

62542312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970934-C-T

62542358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970919-T-G

62542402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970883-G-A

62542402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970883-G-C

62542591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970733-T-C

62542814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8970508-T-A

62543127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8970208-C-G

62543974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8969455-C-T

62544043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8969386-C-T

62544071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8969358-C-T

62545373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8968079-C-T

62545628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967854-G-A

62545628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967854-G-T

62545644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967838-G-A

62545644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967838-G-T

62545652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967830-G-A

62545652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967830-G-T

62545654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967827-G-A

62545654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967827-G-C

62545654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967827-G-T

62545826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967652-T-C

62545826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8967652-T-G

62545927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8967547-G-A

62546182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8967242-A-G

http://identifiers.org/hco/11/GRCh38#62546390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8967062-C-A

http://identifiers.org/hco/11/GRCh38#62546628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#8966823-C-A

62546628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8966823-C-G

http://identifiers.org/hco/11/GRCh38#62546709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8966742-C-A

62546735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8966718-A-G

http://identifiers.org/hco/11/GRCh38#62546814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8966639-C-A

62546814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8966639-C-G

62546873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966590-G-T

62546908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966555-G-A

62546908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966555-G-C

62546908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966555-G-T

http://identifiers.org/hco/11/GRCh38#62546982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8966474-C-A

62546982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966474-C-T

62547116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966337-C-T

62547273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966197-G-A

62547273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966197-G-C

62547273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8966197-G-T

http://identifiers.org/hco/11/GRCh38#62547357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8966119-C-A

62547387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8966089-G-A

62547437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965949-G-C

62547437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965949-G-T

62547438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965948-G-A

62547475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965898-G-A

62547475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965898-G-T

http://identifiers.org/hco/11/GRCh38#62547518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8965811-C-A

62547518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965811-C-G

62547584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965736-T-C

62547600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965720-C-T

62547669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8965650-G-T

http://identifiers.org/hco/11/GRCh38#62547735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#8965586-C-A

62547789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8965536-A-G

62547804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8965526-A-G

62547804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8965526-A-T

62548263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8965101-C-T

62548284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8965080-C-G

62548941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8963570-C-T

62548942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8963569-G-A

62549136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8963391-G-A

62549136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8963391-G-C

62549231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8963297-A-G

62552794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8961503-C-T

62553095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8961253-G-T

62554150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8960301-A-T

62554225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8960223-T-G

62554531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8959950-C-T

62554577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8959905-T-C

62554577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8959905-T-G

62554634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8959837-T-C

62555551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8959124-G-A

62555614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8959078-A-G

62555810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8958899-A-G

62555931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8958782-A-G

62555939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8958773-A-T

62555963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron_variant, undefined
orthologous variants: 8958754-C-T

62556000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: intron variant
orthologous variants: 8958722-C-G

http://identifiers.org/hco/11/GRCh38#62556194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#8958571-C-A

62556234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 347
most severe consequence: 5 prime UTR variant
orthologous variants: 8958536-T-C