161983213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 170510332-T-A

161983213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 170510332-T-G

http://identifiers.org/hco/1/GRCh38#161983302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170510249-C-A

161983357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 170510207-A-G

http://identifiers.org/hco/1/GRCh38#161983388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170510184-A-C

161983388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 170510184-A-G

161983554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 170510019-A-G

161983586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 170509989-A-G

http://identifiers.org/hco/1/GRCh38#161983609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170509958-C-A

161983609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 170509958-C-T

161983647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 170509920-T-C

161983919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 170509648-C-T

161983953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: stop gained
orthologous variants: 170509614-G-A

161983953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170509614-G-C

161984048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170509519-T-C

161984207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170509360-G-A

http://identifiers.org/hco/1/GRCh38#161984234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170509333-C-A

161984234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170509333-C-T

161984285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509283-G-A

161984285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509283-G-C

161984285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509283-G-T

161984286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509282-G-A

161984317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509251-G-A

161984326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509242-G-A

http://identifiers.org/hco/1/GRCh38#161984358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170509233-A-C

http://identifiers.org/hco/1/GRCh38#161984405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170509183-C-A

161984425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170509163-A-G

161984679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508890-T-C

http://identifiers.org/hco/1/GRCh38#161984734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508853-C-A

161984734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508853-C-T

161984735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508852-C-T

161984839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170508745-A-G

161985090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508497-A-G

http://identifiers.org/hco/1/GRCh38#161985107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508480-C-A

161985107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508480-C-T

161985137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508452-T-C

http://identifiers.org/hco/1/GRCh38#161985151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508438-A-C

161985151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508438-A-T

http://identifiers.org/hco/1/GRCh38#161985207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508383-A-C

161985207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508383-A-G

161985207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170508383-A-T

http://identifiers.org/hco/1/GRCh38#161985274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508326-C-A

161985274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508326-C-G

161985303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508296-G-T

161985336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170508258-G-T

http://identifiers.org/hco/1/GRCh38#161985340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170508254-C-A

161985374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170507600-C-T

161985539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170507441-G-T

161985870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170507155-T-G

161986148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506994-G-A

161986148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506994-G-T

161986308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506832-C-T

161986341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506798-G-A

161986363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506776-C-T

161986382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506757-G-A

161986731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506407-C-T

161986733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506405-C-T

http://identifiers.org/hco/1/GRCh38#161986990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170506204-C-A

161987017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170506181-G-A

161987656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170505298-G-C

161987709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170505243-G-C

161987721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170505231-G-A

161987863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170505085-G-A

161987863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170505085-G-C

161988115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170504520-T-C

161988293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170504341-C-T

161988373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170504275-G-A

161988714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503969-C-T

161988766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503943-A-G

161988813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503919-C-T

161988964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503782-A-G

161988988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503759-T-C

161989012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503735-C-T

161989364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503405-G-A

161989566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170503228-G-A

161993832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170502627-G-C

161993846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170502613-C-T

http://identifiers.org/hco/1/GRCh38#161994238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170502257-A-C

161994431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170502065-G-A

161994580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170501920-G-A

161994741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170501775-T-C

161995532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170500274-G-A

161995669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170500139-C-T

161995751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170500062-G-A

161995858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170499956-G-T

161995865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170499949-G-T

161996014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170499836-C-T

161996406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170498623-G-A

161996425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170498590-A-G

161996602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170498421-C-T

161996786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170498132-C-T

http://identifiers.org/hco/1/GRCh38#161997695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170497022-C-A

161997729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496985-G-A

161997729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496985-G-C

161997729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496985-G-T

161997754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496931-T-C

161997891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496764-A-G

161998022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496648-G-A

161998080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496599-C-T

161998152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496509-G-A

161998217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496444-G-A

161998217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170496444-G-C

http://identifiers.org/hco/1/GRCh38#161998455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170496218-C-A

161998455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496218-C-T

161998570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496105-T-C

161998610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496071-G-C

161998614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170496067-T-C

161998958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170495708-T-G

161999247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170495417-C-T

161999344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170495312-A-G

161999372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170495259-A-G

161999688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170494671-G-C

161999824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170494542-C-T

161999855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170494511-G-A

162000190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170494287-G-A

162000191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170494286-A-G

http://identifiers.org/hco/1/GRCh38#162000207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170494270-C-A

162000207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: synonymous variant
orthologous variants: 170494270-C-T

162000430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170494045-A-G

162000449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170494026-A-G

162002511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170493940-C-T

162002645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170493805-A-G

http://identifiers.org/hco/1/GRCh38#162002791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170493634-C-A

162002816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170493604-C-T

162003231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170493209-A-G

162003250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170493190-T-C

162003638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170492805-C-T

162003817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170492650-G-A

162004192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170492283-G-C

162004192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170492283-G-T

162004315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170492131-C-T

162004378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170492070-A-G

162005266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490718-A-G

162005311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490675-G-A

162005326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490660-C-T

162005407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490601-C-T

162005913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490442-A-G

162005913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 170490442-A-T

162005932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490420-T-A

162005932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490420-T-G

162006187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490200-G-A

162006187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490200-G-C

162006187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490200-G-T

162006202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490185-A-G

162006202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490185-A-T

162006203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170490184-G-T

162006289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 170490110-G-A

162006307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170490092-G-A

162006307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170490092-G-T

162006346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170490053-A-T

162006405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170489994-C-G

162006405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: synonymous variant
orthologous variants: 170489994-C-T

http://identifiers.org/hco/1/GRCh38#162006407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#170489992-C-A

162006407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170489992-C-T

162006423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170489976-C-G

162006424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170489975-A-G

162006424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170489975-A-T

162006528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489866-G-A

162006528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489866-G-T

http://identifiers.org/hco/1/GRCh38#162006580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170489753-A-C

162006580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489753-A-G

162006581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489752-G-A

162006581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489752-G-T

http://identifiers.org/hco/1/GRCh38#162006606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170489698-C-A

162006606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489698-C-T

162006647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489657-G-A

162006794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489540-T-C

162006989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489390-C-T

162007327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170489124-G-C

162007580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170487340-G-C

162007833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170487087-T-C

162007941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486992-A-T

162008021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486924-C-T

162008022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486923-G-A

162008022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486923-G-C

162008094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486857-G-A

http://identifiers.org/hco/1/GRCh38#162008150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170486800-C-A

162008150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486800-C-T

162008166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486783-T-C

162008344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486626-G-C

162008395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486191-A-G

162008532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486064-G-A

162008532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170486064-G-C

162008894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170485733-G-A

http://identifiers.org/hco/1/GRCh38#162008962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170485690-C-A

162009006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170485647-C-T

http://identifiers.org/hco/1/GRCh38#162009041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170485614-A-C

162009340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170485345-G-A

162009340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170485345-G-C

162009541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170485133-G-C

http://identifiers.org/hco/1/GRCh38#162009956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170484726-C-A

162009971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484710-C-G

162010057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484633-A-T

162010060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484630-T-G

162010097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484592-T-C

162010408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484315-G-C

http://identifiers.org/hco/1/GRCh38#162010533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170484179-C-A

162010550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484155-C-G

162010550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484155-C-T

162010582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484114-T-G

162010585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484111-T-C

162010605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484091-A-G

162010680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484010-T-G

162010687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170484003-G-C

162010718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483972-T-C

http://identifiers.org/hco/1/GRCh38#162010760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170483939-C-A

162010885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483848-A-G

162010930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483802-G-C

162010963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483778-G-A

162010990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483758-T-C

162011007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483741-A-G

162011009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483739-A-T

http://identifiers.org/hco/1/GRCh38#162011119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170483648-A-C

162011480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483393-G-A

162011533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170483334-A-G

162011893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482992-A-G

http://identifiers.org/hco/1/GRCh38#162012080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170482822-C-A

http://identifiers.org/hco/1/GRCh38#162012103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170482799-C-A

162012204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482702-A-G

162012343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482565-C-T

162012469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482442-G-A

162012573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482369-G-A

162012672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482283-C-T

162012677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482279-T-C

162012688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482268-C-T

162012731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482069-A-G

162012784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482005-A-G

162012784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170482005-A-T

162012807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481986-G-T

http://identifiers.org/hco/1/GRCh38#162012825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170481973-A-C

162012909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481890-G-A

http://identifiers.org/hco/1/GRCh38#162012977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170481828-A-C

162013057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481745-A-T

162013126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481675-T-C

162013158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481643-T-C

162013210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481591-C-T

162013242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481558-G-A

162013277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481525-G-A

162013320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481486-G-A

162013527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481300-G-A

162013541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481286-T-C

162013571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170481258-A-G

162013714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480948-T-C

162013778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480889-T-C

162013822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480845-G-A

http://identifiers.org/hco/1/GRCh38#162013904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170480765-A-C

162014036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480652-A-G

162014135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480313-G-C

162014201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480249-T-C

162014228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480221-C-T

162014429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170480047-T-C

http://identifiers.org/hco/1/GRCh38#162014595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170479882-C-A

162015151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170479323-A-G

162015233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170479253-G-A

162015233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170479253-G-C

162015696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170478832-C-T

162016035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170478390-G-A

162016083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170478275-G-A

http://identifiers.org/hco/1/GRCh38#162016466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170477894-C-A

162016525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477835-T-C

162017347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477464-T-G

162017374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477436-G-C

162017384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477426-C-T

http://identifiers.org/hco/1/GRCh38#162017424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170477386-C-A

162017440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170477370-A-T

http://identifiers.org/hco/1/GRCh38#162017640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170477163-C-A

162017644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477159-T-C

162017645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477158-T-C

162017650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477153-T-A

162017650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477153-T-C

162017650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477153-T-G

162017724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477088-G-A

162017797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170477009-G-C

162018451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476862-T-C

162018470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476843-G-T

http://identifiers.org/hco/1/GRCh38#162018580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170476737-C-A

162018582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476735-C-T

162018708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476611-C-T

http://identifiers.org/hco/1/GRCh38#162018726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170476594-C-A

162018943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476405-A-G

162019010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476338-T-G

162019131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476222-A-G

162019312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476100-T-A

162019384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170476034-G-T

http://identifiers.org/hco/1/GRCh38#162019385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170476033-A-C

162019989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170475442-G-A

http://identifiers.org/hco/1/GRCh38#162020121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170475310-C-A

162020192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475239-C-T

162020207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475200-G-A

162020216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475191-A-G

162020221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475186-A-T

162020244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475174-G-A

162020245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475173-A-G

162020247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475171-G-T

162020249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475169-T-C

162020249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170475169-T-G

162020954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474774-G-A

162021054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474692-G-C

162021213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474516-G-A

162021214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474515-T-A

162021531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474229-A-G

162021584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474189-A-T

162021705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170474064-G-A

162022174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473609-A-G

http://identifiers.org/hco/1/GRCh38#162022177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170473606-A-C

162022646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473468-C-T

162022651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473463-T-C

162022657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473457-G-A

http://identifiers.org/hco/1/GRCh38#162022845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170473262-C-A

162022899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473203-T-C

162022964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473138-C-T

162023009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170473057-G-A

162023114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472804-T-C

162023139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472779-C-G

162023153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472766-A-G

http://identifiers.org/hco/1/GRCh38#162023180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170472739-C-A

162023180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472739-C-T

162023234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472685-G-A

162023234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472685-G-T

162023236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: intron variant
orthologous variants: 170472683-T-A

162023333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: missense variant
orthologous variants: 170472586-T-C

162023443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472476-A-G

162023481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472438-G-A

162023481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472438-G-C

162023501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472420-C-T

162023511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472410-G-A

162023511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472410-G-T

162023535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472384-G-A

162023535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472384-G-T

162023538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472381-T-A

162023538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472381-T-G

http://identifiers.org/hco/1/GRCh38#162023540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170472379-C-A

162023540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472379-C-G

162023540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472379-C-T

162023683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472245-G-A

162023683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472245-G-C

162023683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472245-G-T

162023710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472218-G-A

http://identifiers.org/hco/1/GRCh38#162023711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#170472217-C-A

162023711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472217-C-G

162023711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472217-C-T

162023728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472199-A-G

162023827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472137-G-A

162023827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24558
most severe consequence: 5 prime UTR variant
orthologous variants: 170472137-G-T