http://identifiers.org/hco/2/GRCh38#38067007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013664-C-A

38067007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80013664-C-G

38067007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80013664-C-T

38067079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80013726-T-C

http://identifiers.org/hco/2/GRCh38#38067087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013734-C-A

38067087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80013734-C-T

38067110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80013756-G-A

38067110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80013756-G-T

http://identifiers.org/hco/2/GRCh38#38067130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013776-C-A

38067130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80013776-C-T

38067136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80013782-G-T

http://identifiers.org/hco/2/GRCh38#38067198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013848-A-C

38067267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013914-A-G

38067270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013917-T-C

38067278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013925-G-A

38067278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013925-G-T

38067341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013987-A-G

38067341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013987-A-T

38067477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80014111-C-T

38067536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014302-A-G

http://identifiers.org/hco/2/GRCh38#38067582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80014347-C-A

38067606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014377-G-C

38067606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014377-G-T

38067723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014497-C-T

38067890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014652-A-G

38067952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014714-T-C

38068023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014784-A-G

38068060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014825-G-A

38068060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014825-G-C

38068085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014850-T-C

38068085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014850-T-G

38068134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80014898-C-T

http://identifiers.org/hco/2/GRCh38#38068480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80015198-C-A

38068480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015198-C-T

http://identifiers.org/hco/2/GRCh38#38068917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80015634-C-A

http://identifiers.org/hco/2/GRCh38#38068942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80015654-C-A

38068942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015654-C-G

38068942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015654-C-T

38068943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015655-T-A

38068943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015655-T-C

38068947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015659-A-G

38068947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015659-A-T

http://identifiers.org/hco/2/GRCh38#38068975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80015687-C-A

38069048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015760-G-A

38069057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015769-C-T

38069100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015865-G-A

38069101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80015866-T-G

http://identifiers.org/hco/2/GRCh38#38069181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80015957-A-C

38069190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80015966-G-A

38069293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016120-A-G

38069293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016120-A-T

38069412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016254-A-G

38069696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016534-A-G

38069796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016646-T-G

38069852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016717-T-A

38069910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016784-G-A

38069910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016784-G-T

http://identifiers.org/hco/2/GRCh38#38069930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80016801-C-A

38069930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016801-C-G

38069930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016801-C-T

http://identifiers.org/hco/2/GRCh38#38069971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80016842-C-A

38069971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80016842-C-T

http://identifiers.org/hco/2/GRCh38#38070172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80017042-C-A

http://identifiers.org/hco/2/GRCh38#38070173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80017043-C-A

http://identifiers.org/hco/2/GRCh38#38070256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80017106-C-A

38070256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017106-C-T

38070263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017113-T-A

http://identifiers.org/hco/2/GRCh38#38070267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80017117-C-A

38070300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017147-T-C

38070465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017285-T-C

38070571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017381-G-T

http://identifiers.org/hco/2/GRCh38#38070578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80017388-C-A

38070578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80017388-C-T

38070685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80017486-G-A

38070705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3 prime UTR variant
orthologous variants: 80017506-A-T

38070714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 3 prime UTR variant
orthologous variants: 80017514-C-T

38070732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: missense variant
orthologous variants: 80017532-G-C

38070938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: synonymous variant
orthologous variants: 80017738-G-A

38070938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: synonymous variant
orthologous variants: 80017738-G-T

38071142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80017942-A-G

38071187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80017987-C-T

http://identifiers.org/hco/2/GRCh38#38071247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80018047-C-A

38071247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80018047-C-T

http://identifiers.org/hco/2/GRCh38#38071256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80018056-C-A

38071256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80018056-C-T

38071274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80018074-C-G

38071274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80018074-C-T

http://identifiers.org/hco/2/GRCh38#38071304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80018104-A-C

38071981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80018766-T-C

38072103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80018883-C-T

38072203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80018984-A-T

38072400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019018-T-C

38072447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019068-T-G

38072818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019155-T-C

38072855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019192-G-A

38072944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019278-G-T

http://identifiers.org/hco/2/GRCh38#38073297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80019606-C-A

38073297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019606-C-G

38073297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019606-C-T

38073751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020070-T-C

38073751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020070-T-G

http://identifiers.org/hco/2/GRCh38#38073758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80020077-C-A

38073779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020105-G-C

38073795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020123-T-C

38073795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020123-T-G

38073874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020195-G-A

38073878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020199-T-G

38073951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020250-T-G

38073959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020258-T-G

38074033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020328-A-G

38074050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020345-G-A

38074050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020345-G-T

38074051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020346-T-C

38074051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020346-T-G

38074120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020475-A-T

38074186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020541-A-G

38074186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020541-A-T

38074193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020548-G-A

38074193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020548-G-T

38074238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020599-A-G

38074238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80020599-A-T

38074269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80020637-A-G

38074328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020680-G-A

38074328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80020680-G-C

38074339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80020691-G-T

38074362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80020714-G-C

38074495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80020847-G-A

38074511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80020863-A-G

http://identifiers.org/hco/2/GRCh38#38074550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80020902-C-A

http://identifiers.org/hco/2/GRCh38#38074678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021030-C-A

38074678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021030-C-G

38074705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021057-G-A

38074732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021084-G-C

38074732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021084-G-T

http://identifiers.org/hco/2/GRCh38#38074831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021183-C-A

38074831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021183-C-G

38074894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80021246-G-T

38074927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021279-G-A

38074927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021279-G-C

38074969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021321-G-A

38074969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021321-G-T

38074984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021336-G-A

38074984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021336-G-T

38074996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021348-G-A

38074996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021348-G-C

38074996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021348-G-T

http://identifiers.org/hco/2/GRCh38#38075034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021386-C-A

38075034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021386-C-T

38075044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021396-G-A

38075044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021396-G-C

38075044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021396-G-T

38075107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80021459-T-C

38075176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, synonymous_variant
orthologous variants: 80021528-G-A

38075176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 80021528-G-C

http://identifiers.org/hco/2/GRCh38#38075194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021546-C-A

38075194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80021546-C-T

38075441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021792-G-A

38075441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021792-G-C

38075441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021792-G-T

38075443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021801-G-T

http://identifiers.org/hco/2/GRCh38#38075444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021802-C-A

38075444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021802-C-G

38075444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021802-C-T

http://identifiers.org/hco/2/GRCh38#38075449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021807-C-A

38075449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021807-C-T

http://identifiers.org/hco/2/GRCh38#38075461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021819-C-A

38075461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021819-C-G

38075464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021822-G-T

http://identifiers.org/hco/2/GRCh38#38075465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021823-C-A

38075497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021874-G-A

http://identifiers.org/hco/2/GRCh38#38075534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021911-C-A

38075534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021911-C-T

38075537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021914-T-A

38075537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80021914-T-G

http://identifiers.org/hco/2/GRCh38#38075551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80021926-C-A

38075707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022042-T-C

38075707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022042-T-G

38075757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022093-A-G

http://identifiers.org/hco/2/GRCh38#38075806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80022142-C-A

38075806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80022142-C-T

38075851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022193-G-A

38075851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022193-G-C

38075881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022230-G-A

http://identifiers.org/hco/2/GRCh38#38076019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80022343-C-A

38076019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80022343-C-T

38076051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022375-G-C

38076051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022375-G-T

38076152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022488-A-G

38076216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022553-C-T

38076252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022617-A-G

38076286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022659-G-A

38076286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022659-G-T

38076349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80022728-A-G

http://identifiers.org/hco/2/GRCh38#38076406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80022800-C-A

38076406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80022800-C-T

38076544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80022972-G-A

38076544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80022972-G-T

38076672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023073-A-G

38076847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023213-C-T

38077180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80023507-C-T

38077198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023526-C-T

38077310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80023599-G-A

38077405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023684-T-A

http://identifiers.org/hco/2/GRCh38#38077643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80023867-C-A

38077643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023867-C-G

http://identifiers.org/hco/2/GRCh38#38077717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80023942-C-A

38077717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80023942-C-G

38078378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80024431-G-A

38078378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80024431-G-T

38078403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80024453-T-A

38078553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80024576-C-T

38079032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025004-C-T

38079216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025172-G-C

38079239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025191-C-T

38079324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025276-C-T

http://identifiers.org/hco/2/GRCh38#38079379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80025424-C-A

38079454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025534-C-T

38079691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025859-A-G

38079764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025920-G-A

38079794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025948-G-A

38079794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025948-G-T

38079811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80025965-A-T

38079863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026027-G-A

38079909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026068-A-T

38079958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026109-G-T

38080168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026314-A-G

38080182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026328-G-A

http://identifiers.org/hco/2/GRCh38#38080317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80026421-C-A

38080319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026423-C-T

38080340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026444-G-C

38080544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026610-C-G

38080579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026645-C-T

http://identifiers.org/hco/2/GRCh38#38080678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80026727-C-A

38080696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026746-G-A

http://identifiers.org/hco/2/GRCh38#38080732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80026782-C-A

38080769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026816-G-A

38080769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80026816-G-C

38087602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80027966-T-C

38087646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028004-C-G

38087646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028004-C-T

38087659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028017-C-T

38087765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028195-G-T

38087787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028201-T-A

38087864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028268-C-T

38089262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028835-G-C

38089278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80028850-C-G

38089646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80029203-C-T

38089674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80029231-G-T

38089841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80030194-C-G

38089971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80030334-C-T

38090542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80030739-A-G

38090578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80030770-C-G

38090645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80030843-A-G

38090911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031032-T-C

38090959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031079-C-T

38090985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031103-C-T

38090989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031108-G-C

38090989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031108-G-T

38090997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031116-C-T

38091115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031416-C-G

http://identifiers.org/hco/2/GRCh38#38091141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80031442-C-A

38091216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031497-T-C

38091316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031594-T-C

38091377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031642-T-C

38091600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031853-A-G

38091640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031889-G-A

38091878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80031970-C-G

38091912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032000-C-T

38091964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032050-C-G

38092020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032110-A-G

38092118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032184-C-T

38092208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032269-G-T

38092313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032340-G-A

38092464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032482-C-T

38092870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80032875-G-A

38092929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032905-C-G

38092929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80032905-C-T

http://identifiers.org/hco/2/GRCh38#38092961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80032927-C-A

38093509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80033713-G-A

38093604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80033817-A-G

http://identifiers.org/hco/2/GRCh38#38093632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80033844-C-A

38093632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80033844-C-T

38093668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80033880-C-T

38094053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80034243-C-T

http://identifiers.org/hco/2/GRCh38#38094400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80034583-C-A

38094545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80034724-C-T

38094991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80034773-A-G

38095006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80034789-G-A

http://identifiers.org/hco/2/GRCh38#38095025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80034808-A-C

38095025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80034808-A-G

38095127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80034878-G-C

38095127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80034878-G-T

38095143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80034898-G-T

http://identifiers.org/hco/2/GRCh38#38095239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80034991-C-A

http://identifiers.org/hco/2/GRCh38#38095530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80035242-C-A

38095530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035242-C-T

38095554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035262-C-T

38095724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035432-C-T

38095801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035504-G-T

38095994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035682-C-T

38096005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035693-C-T

38096051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035764-T-C

38096060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035765-C-T

38096105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80035801-C-T

38096182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80035879-C-T

38096207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80035904-G-C

38096701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80036443-C-T

38096783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80036522-G-A

38096878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80036618-A-G

38096880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80036620-T-A

38097037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80036752-C-T

http://identifiers.org/hco/2/GRCh38#38097071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80036784-C-A

38097099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80036812-C-G

http://identifiers.org/hco/2/GRCh38#38097315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80036955-A-C

http://identifiers.org/hco/2/GRCh38#38097318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80036958-C-A

http://identifiers.org/hco/2/GRCh38#38097383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80037017-A-C

http://identifiers.org/hco/2/GRCh38#38097726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80037322-A-C

38097898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80037511-G-C

38097920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80037539-G-C

38098226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80037808-G-C

38098497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80038198-A-G

http://identifiers.org/hco/2/GRCh38#38098537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80038319-C-A

38098697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80038465-G-A

38098697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80038465-G-T

http://identifiers.org/hco/2/GRCh38#38098854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80038620-C-A

38098854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80038620-C-T

38098859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80038633-G-C

http://identifiers.org/hco/2/GRCh38#38098927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80038722-C-A

38098927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80038722-C-G

http://identifiers.org/hco/2/GRCh38#38098997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80038776-C-A

38098997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80038776-C-T

http://identifiers.org/hco/2/GRCh38#38099345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80039136-A-C

38099356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039164-A-G

38099356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039164-A-T

38099536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039308-A-G

38099635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039360-T-C

38099716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039448-G-T

38099769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039543-G-A

38099799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039585-T-C

38099855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039641-T-A

38099855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039641-T-C

38099972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80039756-T-C

38100420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040116-T-G

38100466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040164-C-G

38100485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040189-G-A

38100485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040189-G-T

38100546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040267-C-T

38100585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040295-A-G

38100587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040297-G-A

38100587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040297-G-T

38100593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80040303-T-C

38100681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80040380-C-T

http://identifiers.org/hco/2/GRCh38#38109761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80044059-C-A

38109761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80044059-C-G

38109796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80044097-T-C

38109799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80044100-A-G

http://identifiers.org/hco/2/GRCh38#38109818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80044125-C-A

38109818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80044125-C-T

38109839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80044147-G-A

38109839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2597
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80044147-G-T