54153342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170324557-G-T

54153437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170324655-G-A

54153439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170324657-A-T

54153547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325016-G-A

54153628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325102-A-G

54153700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325177-G-A

54153713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325190-C-T

http://identifiers.org/hco/20/GRCh38#54153897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170325353-C-A

http://identifiers.org/hco/20/GRCh38#54153930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170325381-C-A

54153930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325381-C-G

54153993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325444-A-G

54154047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325502-A-G

54154081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325530-A-G

54154087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325536-G-A

54154087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325536-G-T

54154294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325713-G-T

54154308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325727-G-T

54154318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 170325735-C-T

54154381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170325781-G-T

54154540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170325911-G-A

54154540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170325911-G-T

54154550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170325921-G-T

http://identifiers.org/hco/20/GRCh38#54154588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170325960-C-A

54154594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170325966-T-C

54154633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170326016-T-C

54154698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170326048-G-A

54154698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170326048-G-T

http://identifiers.org/hco/20/GRCh38#54154712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170326062-C-A

54154715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170326066-T-C

54154821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170326135-G-A

54154821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170326135-G-T

54154907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170326217-C-T

54154998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 170326288-G-A

54154998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 170326288-G-T

54155110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 170326409-G-A

54155203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 170326494-C-T

54155305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 170326590-A-G

http://identifiers.org/hco/20/GRCh38#54157123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170327546-C-A

54157124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 170327547-A-T

54157283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170327701-G-A

54157283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170327701-G-C

54157283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170327701-G-T

54157454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 170327873-G-A

54157478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 170327897-A-G

54157562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 170327981-C-T

http://identifiers.org/hco/20/GRCh38#54157580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170327999-C-A

54157580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 170327999-C-T

54157609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170328028-G-A

54157609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170328028-G-T

54157619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170328048-T-C

54157899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170328501-T-A

54157899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170328501-T-C

54157987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170328589-G-T

http://identifiers.org/hco/20/GRCh38#54157996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170328599-C-A

54158019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170328623-T-C

54158057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170328663-A-T

54158116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170328721-T-C

54158438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329317-G-A

54158460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329339-G-T

54158708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329529-G-A

54158834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329654-T-C

54158887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329702-G-A

54158945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329782-A-T

54158971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170329808-C-G

54159013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170329850-C-T

54159040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170329877-A-G

54159137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329974-G-T

54159148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329985-T-C

54159154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329991-T-A

54159154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170329991-T-C

54159743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170330174-T-C

54160007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170330436-G-A

54160039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170330460-A-G

54160204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170330636-G-A

54160239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170330679-C-G

54160642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170331006-T-C

54160873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170331229-G-A

54160912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170331268-C-T

54162578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170331890-G-A

54162578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170331890-G-C

54162578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170331890-G-T

54162612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170331927-A-T

54162643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170331959-T-C

54162648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170331964-T-G

54162668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170331977-A-G

54162669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170331978-A-G

54162701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170332018-T-C

54162701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170332018-T-G

http://identifiers.org/hco/20/GRCh38#54162777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170332095-C-A

54162777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170332095-C-T

http://identifiers.org/hco/20/GRCh38#54162813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170332131-A-C

54162813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170332131-A-G

54162813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170332131-A-T

54162858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170332176-T-C

54162890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332208-A-G

54162890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332208-A-T

54162891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332209-G-A

54162891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332209-G-C

54162891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332209-G-T

54163008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332303-T-C

54163027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332320-A-G

54163330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332794-G-A

54163402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170332855-C-T

54163628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170333051-G-C

54163691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170333100-G-A

54163720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170333128-G-A

http://identifiers.org/hco/20/GRCh38#54164043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170333297-C-A

54164355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170333408-G-A

54164435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170333491-G-C

54164486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170333542-G-A

54164486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170333542-G-T

54164665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170333716-T-C

54164859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334145-A-G

54164937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334220-T-G

54165001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334281-G-A

http://identifiers.org/hco/20/GRCh38#54165591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170334413-C-A

54165607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334424-A-G

54165607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334424-A-T

54165647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334467-T-A

54165648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334468-G-A

54165651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334471-T-C

54165653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334473-C-T

54165757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170334568-G-A

54165757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170334568-G-T

54165778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous variant
orthologous variants: 170334589-C-T

54165839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 170334650-A-G

54165839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 170334650-A-T

http://identifiers.org/hco/20/GRCh38#54165851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170334662-C-A

54165851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334662-C-T

54165904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334712-A-G

54165904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334712-A-T

54165935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170334743-T-A

54166309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335020-G-T

54166316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335027-T-A

54166319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335030-C-T

54169267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335704-G-C

54169476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335887-C-T

54169560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170335975-A-T

54169669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense variant
orthologous variants: 170336073-C-T

http://identifiers.org/hco/20/GRCh38#54169745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170336145-C-A

54169745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336145-C-G

54169805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336175-G-T

http://identifiers.org/hco/20/GRCh38#54169814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170336184-C-A

54169893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336231-G-A

54170985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336678-A-G

54171017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336703-C-G

54171044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336729-A-G

http://identifiers.org/hco/20/GRCh38#54171104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170336797-C-A

54171123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336822-C-T

54171279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170336983-G-A

54171413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337081-G-T

54171432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337092-G-A

54171518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337182-C-T

54171607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense variant
orthologous variants: 170337274-T-G

54171686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, missense_variant
orthologous variants: 170337349-G-A

http://identifiers.org/hco/20/GRCh38#54171688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#170337351-A-C

54171688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 170337351-A-G

http://identifiers.org/hco/20/GRCh38#54171786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170337421-C-A

54171786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170337421-C-G

54171786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170337421-C-T

54172586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170337797-T-A

54172597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, undefined
orthologous variants: 170337808-A-G

54172742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337943-G-A

54172742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337943-G-T

54172796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron variant
orthologous variants: 170337999-A-G

54172855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170338048-C-T

http://identifiers.org/hco/20/GRCh38#54172856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338049-C-A

54172856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170338049-C-G

54172856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170338049-C-T

54172867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170338062-T-A

http://identifiers.org/hco/20/GRCh38#54172868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338063-C-A

54172868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170338063-C-T

54172871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 170338066-G-T

54172886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 170338078-C-T

54172926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170338111-G-A

54172987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170338172-G-A

54172987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170338172-G-T

54173033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170338218-G-A

54173033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 170338218-G-T

54173076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 170338261-G-T

http://identifiers.org/hco/20/GRCh38#54173120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338305-C-A

54173120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170338305-C-G

54173120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170338305-C-T

http://identifiers.org/hco/20/GRCh38#54173166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338345-C-A

54173166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170338345-C-T

http://identifiers.org/hco/20/GRCh38#54173170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338349-C-A

http://identifiers.org/hco/20/GRCh38#54173171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338350-C-A

54173171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170338350-C-T

http://identifiers.org/hco/20/GRCh38#54173214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338377-C-A

54173214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 170338377-C-G

54173214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 170338377-C-T

54173283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 170338402-A-T

54173300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 170338419-A-G

54173356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 170338471-C-T

54173361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170338476-A-G

http://identifiers.org/hco/20/GRCh38#54173406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338521-C-A

54173406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170338521-C-G

54173406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 170338521-C-T

http://identifiers.org/hco/20/GRCh38#54173435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338550-C-A

54173435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338550-C-T

54173479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338594-G-A

54173479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338594-G-C

54173479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338594-G-T

54173480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338595-T-A

http://identifiers.org/hco/20/GRCh38#54173490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338605-A-C

54173490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous_variant, undefined
orthologous variants: 170338605-A-G

54173498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense variant
orthologous variants: 170338613-C-G

54173498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense variant
orthologous variants: 170338613-C-T

http://identifiers.org/hco/20/GRCh38#54173524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338639-C-A

54173524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: missense_variant, undefined
orthologous variants: 170338639-C-T

54173544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous_variant, undefined
orthologous variants: 170338659-G-A

54173544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: synonymous_variant, undefined
orthologous variants: 170338659-G-T

54173588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338703-G-C

54173588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338703-G-T

54173650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: 170338766-T-A

54173705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338821-T-C

54173714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338830-G-A

54173714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338830-G-C

54173714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338830-G-T

54173734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: 170338838-G-A

54173734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: 170338838-G-T

http://identifiers.org/hco/20/GRCh38#54173811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338921-C-A

54173811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: 170338921-C-T

54173880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338967-G-A

54173880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170338967-G-T

http://identifiers.org/hco/20/GRCh38#54173886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338973-C-A

54173886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5 prime UTR variant
orthologous variants: 170338973-C-G

http://identifiers.org/hco/20/GRCh38#54173898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170338985-C-A

http://identifiers.org/hco/20/GRCh38#54173932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#170339012-C-A

54173932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170339012-C-G

54173932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2602
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 170339012-C-T