29501289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134299-T-C

29501415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134424-C-T

29501584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134577-G-A

http://identifiers.org/hco/12/GRCh38#29501894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148134870-C-A

29501901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134877-T-C

29501901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134877-T-G

http://identifiers.org/hco/12/GRCh38#29502015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148134977-A-C

29502015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148134977-A-T

http://identifiers.org/hco/12/GRCh38#29502092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148135048-C-A

http://identifiers.org/hco/12/GRCh38#29502282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148135231-A-C

http://identifiers.org/hco/12/GRCh38#29502309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148135254-A-C

29502397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148135548-C-T

http://identifiers.org/hco/12/GRCh38#29502604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148135776-C-A

29502737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148135906-T-C

29503002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136108-C-T

29503010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136116-C-T

http://identifiers.org/hco/12/GRCh38#29503091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148136193-C-A

29503091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136193-C-T

http://identifiers.org/hco/12/GRCh38#29503405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148136488-C-A

29503420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136503-A-G

29503534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136592-A-G

http://identifiers.org/hco/12/GRCh38#29503590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148136634-A-C

29503656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136695-T-C

29503656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136695-T-G

29503852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136781-G-A

29503852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136781-G-T

29503926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136803-A-G

29503926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148136803-A-T

29504897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148137512-T-C

29505130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148137686-G-A

29505403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148137931-C-T

29505651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148138149-T-C

29505960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3 prime UTR variant
orthologous variants: 148138434-G-A

29506056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138527-G-A

29506056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138527-G-T

http://identifiers.org/hco/12/GRCh38#29506314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148138824-C-A

29506352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138859-T-C

29506365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138872-T-C

29506383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138888-A-T

29506420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138923-G-T

29506461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138946-G-T

29506501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148138984-G-T

29506687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139150-G-A

29506687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139150-G-T

29506719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139180-G-T

29506737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139187-T-A

29506737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139187-T-C

29506743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148139193-A-G

29507351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148139772-G-A

29508603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148141434-T-G

29508955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148141491-T-C

29509249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148141730-C-G

29511023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148143338-C-G

29511241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148143501-G-A

29511496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148143711-C-G

29511994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148144677-A-G

29512174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148144822-A-G

http://identifiers.org/hco/12/GRCh38#29512178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148144826-C-A

29512178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148144826-C-T

29514016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148145794-C-T

29514050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148145828-G-A

29514153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148145887-G-C

29514158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148145892-T-C

29514564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148146264-T-C

29514564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148146264-T-G

http://identifiers.org/hco/12/GRCh38#29514581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148146281-A-C

29514581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148146281-A-G

29515836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148146773-A-G

29516293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147115-T-C

29516293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147115-T-G

29516294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147116-G-A

29516430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 148147290-G-A

29516550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147413-T-C

29516550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147413-T-G

http://identifiers.org/hco/12/GRCh38#29516620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148147463-C-A

29516620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148147463-C-T

29516732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148147559-T-G

29517442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148148247-C-G

http://identifiers.org/hco/12/GRCh38#29517529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148148334-C-A

http://identifiers.org/hco/12/GRCh38#29517604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148148407-C-A

29517633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148148434-G-C

29517633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148148434-G-T

29518168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148148629-A-G

29518355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148148786-T-C

29518558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148148987-G-A

29518558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148148987-G-C

29518558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148148987-G-T

29518600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148149029-T-C

http://identifiers.org/hco/12/GRCh38#29518700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148149124-C-A

29518700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148149124-C-T

29518886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148149304-T-C

29519234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148149790-C-T

29519423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148149979-A-G

29519444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148150000-T-A

29520270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148150712-T-A

29520390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148150817-C-T

29520734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148151098-G-A

29520734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148151098-G-C

29520890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148151231-A-G

29520896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148151237-T-A

29520896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148151237-T-C

http://identifiers.org/hco/12/GRCh38#29520937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148151280-C-A

29520937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148151280-C-T

http://identifiers.org/hco/12/GRCh38#29520949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148151292-A-C

29521394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148152044-C-T

29529626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148153850-C-T

29529718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148153960-C-T

http://identifiers.org/hco/12/GRCh38#29531128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148155168-C-A

29531720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148156249-T-C

29531729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148156258-C-T

29533882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148157736-G-T

http://identifiers.org/hco/12/GRCh38#29533985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148157835-C-A

29533985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148157835-C-T

29533990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148157840-G-A

29533990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148157840-G-T

29534045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148157866-A-G

http://identifiers.org/hco/12/GRCh38#29534180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148157986-C-A

29534310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158113-A-G

29534477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158288-A-G

29534479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158290-A-G

29534501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158307-G-A

29534617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158428-G-T

29534624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148158435-C-T

29536185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148164248-A-G

29536215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148164287-A-T

29536289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148164361-T-G

29536348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164410-A-G

29536350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164412-A-G

29536350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164412-A-T

29536424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164484-G-T

29536429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164489-A-G

29536448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164509-T-C

29536448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164509-T-G

http://identifiers.org/hco/12/GRCh38#29536502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148164670-C-A

29536549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164797-A-G

29536599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148164963-C-G

29536796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148165354-G-T

29536940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148165485-G-A

29537068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148165568-A-T

29537127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148165611-A-G

29537619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148166637-C-T

29537696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148166683-T-C

29543065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148168514-G-A

29543130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148168582-G-A

29543433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148168857-G-A

http://identifiers.org/hco/12/GRCh38#29543476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148168895-C-A

29543574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148169472-T-C

29543583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148169480-T-A

http://identifiers.org/hco/12/GRCh38#29544104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148169738-C-A

29544104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148169738-C-T

29544247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148169868-A-G

29544491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148170160-G-T

29544632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148170285-A-G

29553337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171391-A-G

29553588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171600-A-G

29553833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171793-T-A

29553909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171856-C-T

29553953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171898-C-T

29554008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148171953-A-G

29556788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148172822-G-A

29556788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148172822-G-T

http://identifiers.org/hco/12/GRCh38#29556976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148172993-C-A

29556976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148172993-C-T

29557407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148173365-C-T

29558044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148173631-G-A

29561210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148174028-A-G

29561222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148174040-G-T

29561359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148174191-T-G

29562160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148175563-T-C

29566636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148179774-G-C

29566821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148179905-G-A

29567042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148180104-G-T

29567177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148180237-T-C

29567326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148180383-G-A

29567396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148180452-T-G

29567939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148180971-T-C

29568128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148181159-T-C

29568550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148183448-A-T

29569436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185067-C-T

29569487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185116-G-T

29569519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185148-C-T

29569564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185191-T-C

29570097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185670-A-G

29570233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148185792-C-T

http://identifiers.org/hco/12/GRCh38#29571996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148186259-C-A

29571996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186259-C-T

29572002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186265-A-G

29572060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186315-G-T

29572083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186337-A-T

29572095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186345-T-C

29572237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186483-T-A

29572592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186807-T-C

29572721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186935-G-A

29572721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186935-G-C

http://identifiers.org/hco/12/GRCh38#29572736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148186949-C-A

29572736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186949-C-G

29572736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148186949-C-T

29572932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148187144-C-T

29573518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148187572-G-A

29573627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148187677-G-A

29573692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148187744-G-A

29574040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148188254-G-C

29574175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148188331-C-T

29574742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148188826-C-T

29574787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148188867-T-C

29574845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148188920-G-A

29575012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148189091-A-T

29575124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148189210-A-T

29575219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148189305-T-C

29575889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148189837-A-G

29576434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148190176-A-G

29576543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148190262-C-T

http://identifiers.org/hco/12/GRCh38#29578781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148191181-C-A

29579117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148191435-C-T

29580936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148191611-T-C

29581450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192022-A-T

29581590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192187-G-A

29581706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192331-G-A

29581738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192362-G-A

29581738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192362-G-T

29581741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192365-C-T

29581877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192492-A-G

29581964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148192570-C-G

29583071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195615-T-C

29583136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195698-T-A

29583247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195797-T-G

29583328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195874-G-A

29583328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195874-G-T

29583354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195897-T-A

29583387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148195930-T-G

29583433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148196039-A-G

http://identifiers.org/hco/12/GRCh38#29583490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148196096-C-A

29591012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148198546-T-C

http://identifiers.org/hco/12/GRCh38#29591025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148198562-A-C

29591149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148198697-A-T

29591339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148198879-G-A

29591851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148199482-T-C

29592172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148199823-C-G

29592271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148199906-C-T

29592457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200085-A-G

29592481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200103-T-C

29592496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200118-G-A

29592532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200153-G-A

29592953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200586-C-T

http://identifiers.org/hco/12/GRCh38#29592975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148200603-A-C

29593167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148200715-G-A

http://identifiers.org/hco/12/GRCh38#29593262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148200791-A-C

29598968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148203337-C-T

29599040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148203408-G-C

http://identifiers.org/hco/12/GRCh38#29599478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148203842-C-A

29599501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148203868-A-G

29599620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148203986-T-G

29599696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148204060-G-T

29599716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148204076-T-C

29601027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206562-C-T

29601028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206563-G-A

29601028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206563-G-T

29601105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206640-C-G

29601105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206640-C-T

29603554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148206908-T-G

29603680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207017-C-T

http://identifiers.org/hco/12/GRCh38#29604072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148207412-C-A

29604072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207412-C-T

29604073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207413-C-T

29604109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207451-C-T

29604313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207631-T-C

29604336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207655-G-A

29604336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207655-G-T

29604565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207835-G-A

29604663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148207910-A-G

29604826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148208052-T-A

29604826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148208052-T-C

http://identifiers.org/hco/12/GRCh38#29605596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148210295-C-A

29605596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148210295-C-T

29609669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148211180-A-G

29609730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148211237-A-G

http://identifiers.org/hco/12/GRCh38#29609800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148211300-C-A

29609852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 148211326-T-C

http://identifiers.org/hco/12/GRCh38#29610432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148211970-A-C

29610461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148212001-T-C

29610480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148212020-T-A

29610480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148212020-T-C

29611180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148212703-T-C

29611428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148212963-A-G

29611509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148213030-G-A

29611509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148213030-G-C

29611572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148213092-T-C

29611854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148213366-G-A

29613765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216106-C-G

29613765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216106-C-T

29613773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216114-T-C

29613782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216126-C-G

29613795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216136-G-T

29613839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216197-G-C

29613839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216197-G-T

29614018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216344-G-T

29614099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216425-C-T

29614178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148216500-G-A

29620255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148221009-G-C

29620694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148221155-G-A

29621175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148224332-T-G

29621373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148224493-C-T

29621389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148224509-T-C

29621664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148224833-T-G

29621752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148224913-G-C

29621926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148225084-G-A

29621976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148225128-G-A

29632882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148226091-C-G

http://identifiers.org/hco/12/GRCh38#29632888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148226097-A-C

29633045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148226512-G-T

29633230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148226698-T-C

29633267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148226735-A-G

29633571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148227004-T-C

29633632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148227060-T-C

http://identifiers.org/hco/12/GRCh38#29634151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148227629-C-A

29634192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148227670-T-C

29634258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148227731-T-C

29634515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148228200-C-T

29653298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148232667-T-C

29655917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148233394-G-C

29655929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148233406-G-A

29656027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148233505-G-T

29656924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148234339-C-G

29657157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148234569-C-G

29657157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148234569-C-T

29657376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148235271-C-T

29657506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148235381-C-T

29657657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148235696-A-G

29657682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148235728-G-C

29658842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236297-G-A

29658842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236297-G-T

29658905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236354-A-G

29659007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236423-T-C

29659150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236554-C-T

29659702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236870-T-C

29659775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236948-T-G

29659802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236983-G-A

29659802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148236983-G-T

29659847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148237104-A-G

29659995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148237256-A-G

http://identifiers.org/hco/12/GRCh38#29660026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148237286-C-A

http://identifiers.org/hco/12/GRCh38#29660030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148237290-A-C

29660846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148237791-G-A

29660846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148237791-G-T

29661012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148237939-G-A

29661012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148237939-G-T

29662794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148242937-G-C

29664443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148243879-T-C

29664590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148243989-A-G

29664855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148244316-T-C

29665419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148245247-C-T

29665632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148245458-G-C

29665960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246134-C-G

29666088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246257-T-C

29666240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246406-T-C

29666352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246484-T-A

29666352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246484-T-C

http://identifiers.org/hco/12/GRCh38#29666384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148246495-A-C

29666384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246495-A-T

29666407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246518-G-T

29666434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246533-T-C

29666683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246848-G-T

29666778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148246940-C-T

29666943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148247125-A-G

29667197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148247319-C-G

29667493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148247608-T-C

29667549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148247665-A-T

29669197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148249928-C-G

29669422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250218-T-C

29669431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250224-A-G

29669586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250353-C-T

29669785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250520-C-T

29669800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250524-T-C

http://identifiers.org/hco/12/GRCh38#29669935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148250606-C-A

http://identifiers.org/hco/12/GRCh38#29670037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148250723-C-A

29670037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250723-C-T

29670234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250905-G-A

29670282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250950-C-T

29670335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148250989-C-T

http://identifiers.org/hco/12/GRCh38#29670558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148251205-C-A

29671894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148251817-G-A

29672147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148251999-T-G

29672274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148252129-T-C

29672290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148252144-T-C

29672579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148252714-T-C

29672789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148252886-G-A

29674618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148253178-G-T

29674819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148253365-C-G

29674935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148253457-A-G

29675834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148254464-T-C

http://identifiers.org/hco/12/GRCh38#29684044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148257752-A-C

29689824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148260487-T-A

29690155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148260802-C-G

29690155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148260802-C-T

29690199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148260853-G-A

29690709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148261358-T-C

29692214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148262576-C-T

29692228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148262588-T-C

29692713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148263104-C-T

http://identifiers.org/hco/12/GRCh38#29692789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148263133-C-A

29693024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148263335-G-A

29693728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148263471-A-G

29693811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148263547-G-A

29695971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148264676-T-G

29696174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148264861-C-T

29696240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148264917-C-T

29696574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148265411-T-C

http://identifiers.org/hco/12/GRCh38#29696891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148265802-C-A

29698743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148268534-C-T

29698949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148268742-C-T

29699142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148268929-T-C

29699143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148268930-A-G

29699265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148269098-C-G

29700800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148273029-G-A

29700970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148273187-G-T

29701738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148273898-A-T

29701780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148273933-G-A

29702122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148274572-G-A

29702315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148274975-A-T

29702518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275156-G-A

29702518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275156-G-C

29702703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275291-C-T

29702832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275431-T-C

http://identifiers.org/hco/12/GRCh38#29703163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#148275488-C-A

29703163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 148275488-C-G

29703467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275776-T-C

29703648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148275951-C-T

29704547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148276363-C-T

29705116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148277274-G-A

http://identifiers.org/hco/12/GRCh38#29705150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148277307-C-A

29707271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148279980-T-C

29707369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148282500-G-A

29707886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148282784-G-A

29707999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148282844-G-A

29708139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148282979-G-T

29708376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148283219-C-T

29708481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148283318-C-T

29709933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148285916-G-A

29709966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148285949-G-A

29710250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148286200-C-G

29710287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148286233-T-C

29710426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148286379-C-T

29720141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290525-G-A

29720219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290600-T-C

29720241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290622-G-T

29720270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290733-T-C

29720301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290764-G-A

29720342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148290800-C-T

29720676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291118-T-A

29720676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291118-T-G

29720684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291126-T-A

29720684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291126-T-C

29720823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291246-C-T

29720843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148291269-C-T

29725566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148292102-T-C

http://identifiers.org/hco/12/GRCh38#29725935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148292452-C-A

http://identifiers.org/hco/12/GRCh38#29726379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148292845-A-C

29726678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148293105-C-T

29726853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148293605-T-C

29727006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148293753-T-C

29728320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148294533-C-T

http://identifiers.org/hco/12/GRCh38#29728333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148294546-A-C

29728334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148294547-G-A

http://identifiers.org/hco/12/GRCh38#29729579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148295063-C-A

29729579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295063-C-T

29729628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295111-G-A

29729749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295219-A-G

29729858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295299-C-T

29729988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295425-G-T

29730034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295470-G-A

29730139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295566-T-C

29730159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295585-G-A

29730296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295728-G-T

29730423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295811-G-A

29730554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148295948-C-G

http://identifiers.org/hco/12/GRCh38#29730759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148296160-C-A

29730985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148296358-G-A

29730995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148296368-C-T

29730996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148296369-A-G

29731472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148297282-G-A

29731487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148297297-T-C

29731999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148297860-C-T

29732225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148298037-A-T

29732388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148298283-C-T

http://identifiers.org/hco/12/GRCh38#29733553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148298621-A-C

29733579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148298637-C-G

29733901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148298937-C-G

29733901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148298937-C-T

29733991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299026-A-T

29734035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299069-T-C

29734115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299132-T-G

29734181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299536-A-G

29734283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299642-G-A

29734349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148299710-C-G

29734853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148300434-G-A

29734888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148300472-C-T

29735324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148300819-T-A

29735366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148300860-C-T

29735729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301209-T-G

29735739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301219-T-C

http://identifiers.org/hco/12/GRCh38#29735838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148301301-C-A

29735838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301301-C-T

29735868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301330-G-C

29735927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301387-G-T

29736173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301626-C-G

http://identifiers.org/hco/12/GRCh38#29736229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148301674-C-A

29736237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301682-G-A

29736237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148301682-G-T

29737631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148302286-G-T

29737811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148302681-A-G

29737896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148302753-C-T

29737940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148302797-T-A

29738220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148303027-C-T

29738360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148303160-A-G

29738675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148303473-C-T

29738756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148303550-T-C

29739421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148304560-G-A

29739421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148304560-G-T

29739468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148304611-T-C

29739646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148304721-G-T

29740851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148305064-G-T

http://identifiers.org/hco/12/GRCh38#29741602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148306083-A-C

http://identifiers.org/hco/12/GRCh38#29741608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148306089-C-A

29741898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148306373-G-T

http://identifiers.org/hco/12/GRCh38#29742010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148306506-A-C

http://identifiers.org/hco/12/GRCh38#29742086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148306556-C-A

29742318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148306730-T-A

29742320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148306732-T-C

29742331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148306743-T-C

29742783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148307253-C-T

29742809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148307278-T-C

29743208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148307669-G-A

29743416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148307850-T-C

29743417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148307851-G-C

29743883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308284-G-A

29743884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308285-G-C

29744001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308405-G-C

29744055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308458-T-C

29744206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308606-C-T

29744600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308849-A-G

http://identifiers.org/hco/12/GRCh38#29744606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148308855-C-A

29744686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148308940-G-T

http://identifiers.org/hco/12/GRCh38#29744697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148308951-A-C

29744996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148309201-G-C

29745262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148309707-T-C

29747031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148310236-G-A

29747274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148310462-G-A

http://identifiers.org/hco/12/GRCh38#29747470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148310644-C-A

29747750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148310851-G-A

29748719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148311661-C-T

http://identifiers.org/hco/12/GRCh38#29748979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148311872-C-A

29748979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148311872-C-T

29751565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148312451-A-G

http://identifiers.org/hco/12/GRCh38#29751658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148312528-C-A

29751658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 148312528-C-G

29751658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 148312528-C-T

http://identifiers.org/hco/12/GRCh38#29751839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148312706-C-A

29751841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 148312708-G-A

29752041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148312903-A-G

29755032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148313591-C-T

29755264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148313822-C-T

29755351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148313919-T-C

29755559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314052-T-C

29755559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314052-T-G

29755683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314114-G-A

29755683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314114-G-T

http://identifiers.org/hco/12/GRCh38#29755756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148314187-C-A

http://identifiers.org/hco/12/GRCh38#29755768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148314199-C-A

29755768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148314199-C-T

http://identifiers.org/hco/12/GRCh38#29755932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148314405-C-A

29755932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314405-C-G

29756255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314911-G-A

29756343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148314965-G-A

29756977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148315761-C-T

29757052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148315809-A-T

http://identifiers.org/hco/12/GRCh38#29757294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148316038-C-A

29758667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317168-T-C

http://identifiers.org/hco/12/GRCh38#29758676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148317180-A-C

29758766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148317270-G-A

29758766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148317270-G-T

29758859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317351-A-G

29759043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317517-T-G

29759579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317840-A-G

29759628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317876-A-G

29759717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148317962-C-T

http://identifiers.org/hco/12/GRCh38#29759870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148318114-C-A

29760105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318295-G-C

29760196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318348-T-C

29760203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318355-A-G

29760444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318454-C-T

29760867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318850-T-G

29760894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318878-T-C

29760930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148318912-T-A

29761031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148319006-G-T

29761041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148319016-G-A

29761041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148319016-G-T

29761111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148319062-A-G

29761180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148319117-T-C

29762596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148320365-G-A

29762801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321326-G-A

29762853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321360-T-C

29763072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321544-G-C

29763130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321602-C-T

29763151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321623-T-C

29763163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321634-T-G

29763290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148321880-T-G

29763415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322000-C-T

http://identifiers.org/hco/12/GRCh38#29763602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148322165-A-C

29763661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322199-A-T

29763674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322212-G-T

29763703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322243-T-C

29763900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322395-A-T

29763931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148322427-G-C

29764754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148324187-T-G

29764763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148324196-C-T

29764997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148324576-T-C

29765420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325065-C-G

29765521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325177-T-C

http://identifiers.org/hco/12/GRCh38#29765661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148325413-A-C

29765954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325687-G-A

29765954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325687-G-C

29766124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325859-C-G

29766132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148325867-A-G

29766326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326199-G-A

http://identifiers.org/hco/12/GRCh38#29766469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148326338-C-A

29766469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326338-C-T

29766477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326344-A-G

29766584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326460-T-C

29766588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326464-A-G

29766789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326646-C-G

29766789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326646-C-T

29767362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326946-A-G

29767394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148326978-G-C

29767492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327044-T-C

29767585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327118-G-A

29767627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327142-G-T

29767746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327227-T-A

http://identifiers.org/hco/12/GRCh38#29767955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148327362-A-C

http://identifiers.org/hco/12/GRCh38#29768036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148327443-A-C

29768036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148327443-A-G

http://identifiers.org/hco/12/GRCh38#29768129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148327541-A-C

http://identifiers.org/hco/12/GRCh38#29768135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148327547-A-C

29768135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327547-A-G

29768135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327547-A-T

http://identifiers.org/hco/12/GRCh38#29768165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148327570-A-C

29768470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327822-A-T

29768479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148327831-C-T

http://identifiers.org/hco/12/GRCh38#29768778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148328339-A-C

29769078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148328977-C-G

29769088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148328987-C-G

29769088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148328987-C-T

29769143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148329041-T-C

29769181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148329079-C-G

29773096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148332751-T-C

29773179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148332796-C-T

29773210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148332832-G-A

http://identifiers.org/hco/12/GRCh38#29773477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148333083-C-A

29773557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148333155-G-A

29773557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148333155-G-C

29773588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148333185-T-C

http://identifiers.org/hco/12/GRCh38#29774759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148334970-C-A

29774877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148335053-G-C

29775437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336029-G-A

29775439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336031-T-C

29775738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336322-C-G

29775781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336362-A-G

29776087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336695-G-A

29776096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336709-G-C

29776207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336796-C-T

29776223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336812-C-T

29776270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336860-C-T

29776282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336872-C-T

29776411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148336974-C-G

29776742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148338093-G-A

29776767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148338110-C-T

29776774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148338117-G-A

29776845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148338187-T-G

29777063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148338365-T-C

http://identifiers.org/hco/12/GRCh38#29778560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148340601-A-C

29778577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148340621-A-G

29778601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148340648-T-C

29778644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148340691-A-T

29778648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148340695-T-C

29779692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341551-T-C

29780490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341826-G-A

29780490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341826-G-C

29780492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341828-G-A

29780492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341828-G-C

29780618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341947-T-C

29780619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148341948-G-A

29780701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148342022-A-G

29781909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148343611-T-C

29782048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148343740-T-G

29782286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148343991-T-C

29782693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148344299-G-A

29782693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148344299-G-T

29782749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148344354-A-T

http://identifiers.org/hco/12/GRCh38#29782816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148344416-C-A

29782816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148344416-C-T

29782893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148344485-G-A

29782966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148344560-G-A

29782966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148344560-G-T

29783300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345023-G-A

29783300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345023-G-T

http://identifiers.org/hco/12/GRCh38#29783351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345186-A-C

29783351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345186-A-G

29783351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345186-A-T

http://identifiers.org/hco/12/GRCh38#29783359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345228-C-A

29783359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345228-C-T

29783493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant
orthologous variants: 148345442-T-A

29783493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant
orthologous variants: 148345442-T-C

29783493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant
orthologous variants: 148345442-T-G

29783569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 148345518-G-A

29783569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 148345518-G-C

29783569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 148345518-G-T

http://identifiers.org/hco/12/GRCh38#29783685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345634-C-A

29783685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 148345634-C-G

29783685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 148345634-C-T

http://identifiers.org/hco/12/GRCh38#29783687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345636-C-A

29783687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 148345636-C-G

29783687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 148345636-C-T

http://identifiers.org/hco/12/GRCh38#29783718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345667-C-A

29783718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, missense_variant
orthologous variants: 148345667-C-T

29783764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345710-G-A

29783764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345710-G-T

29783796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345730-G-A

29783796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345730-G-T

29783812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345746-G-A

29783812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345746-G-C

29783812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345746-G-T

29783814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148345748-G-T

http://identifiers.org/hco/12/GRCh38#29783963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148345872-C-A

29783963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345872-C-G

29783963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345872-C-T

29784078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148345988-C-T

29784139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron variant
orthologous variants: 148346045-G-A

http://identifiers.org/hco/12/GRCh38#29784298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#148346186-C-A

29784298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: intron_variant, undefined
orthologous variants: 148346186-C-T

29784325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 148346213-G-T

29784337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 148346219-C-T

http://identifiers.org/hco/12/GRCh38#29784427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148346351-C-A

29784427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5 prime UTR variant
orthologous variants: 148346351-C-G

29784427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24099
most severe consequence: 5 prime UTR variant
orthologous variants: 148346351-C-T