103859279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron_variant, undefined
orthologous variants: 47455198-T-C

103859310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47455238-T-C

103859856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47457456-T-C

103859937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47457581-G-A

103860374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47458762-G-A

103860374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47458762-G-C

103860456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47458867-A-G

103860500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47458910-A-G

103860500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47458910-A-T

103860633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47459055-A-G

103860663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47459074-T-C

103862101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461153-C-T

103862270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461318-A-G

103862291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461339-A-G

103862639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461734-A-T

103862644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461736-T-C

http://identifiers.org/hco/10/GRCh38#103862771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47461861-A-C

103862771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461861-A-G

103862801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47461891-G-C

103867585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474193-G-A

103867585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474193-G-T

103867633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474240-T-C

103867634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474241-G-A

103867881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474499-A-G

103867881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474499-A-T

http://identifiers.org/hco/10/GRCh38#103867902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47474515-A-C

103867909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474522-A-G

103868128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474720-T-G

103868346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47474937-G-A

103868504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47475082-T-C

http://identifiers.org/hco/10/GRCh38#103868511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47475089-A-C

103868555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47475139-G-A

103868555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47475139-G-T

103868818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47475386-C-T

103869576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47476279-C-G

http://identifiers.org/hco/10/GRCh38#103869601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47476304-C-A

103869612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47476315-G-A

103869653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47476355-C-T

103869884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47476555-G-A

103871062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47479945-A-G

103871081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47479964-C-T

103871142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480018-G-A

103871178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480043-C-T

103871225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480074-T-C

103871594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480123-C-T

103871676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480207-T-A

103871768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480284-T-C

http://identifiers.org/hco/10/GRCh38#103871772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47480288-C-A

http://identifiers.org/hco/10/GRCh38#103872203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47480339-C-A

103872234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480370-C-G

103872234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480370-C-T

103872424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480595-T-C

103872424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480595-T-G

103872638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47480854-A-G

103872841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481164-C-T

103872875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481195-T-C

103872923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481234-T-C

103873451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481445-A-T

103873602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481574-T-A

http://identifiers.org/hco/10/GRCh38#103874026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47481780-C-A

103874108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47481853-A-G

103874340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47482070-C-T

103874637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47482347-T-C

103874904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47483518-G-A

103874904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: intron variant
orthologous variants: 47483518-G-C

103877953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47485802-T-G

http://identifiers.org/hco/10/GRCh38#103878129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47485978-C-A

103878129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47485978-C-T

103878155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486004-C-T

http://identifiers.org/hco/10/GRCh38#103878285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47486128-C-A

http://identifiers.org/hco/10/GRCh38#103878302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47486143-C-A

103878302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486143-C-G

103878380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486227-T-C

http://identifiers.org/hco/10/GRCh38#103878405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47486251-C-A

103878410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486256-G-T

http://identifiers.org/hco/10/GRCh38#103878477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47486291-C-A

103878718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486964-G-A

103878723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47486969-C-T

103878776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487092-A-G

103878844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487164-G-A

103878844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487164-G-T

103878864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487182-A-G

103878873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487191-G-A

103878873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487191-G-T

103878947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487258-G-T

103878994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487293-A-G

103879025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487324-A-G

http://identifiers.org/hco/10/GRCh38#103879054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47487352-C-A

103879054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487352-C-T

103879069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487367-G-A

103879080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487379-G-A

103879088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487387-A-G

http://identifiers.org/hco/10/GRCh38#103879121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47487419-C-A

103879121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487419-C-T

http://identifiers.org/hco/10/GRCh38#103879157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47487447-C-A

103879359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487623-G-A

103879359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487623-G-T

103879409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487652-T-C

103879430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487669-G-T

http://identifiers.org/hco/10/GRCh38#103879447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47487686-C-A

103879489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487713-G-A

103879489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487713-G-T

103879597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487796-G-T

103879670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487874-G-A

103879670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487874-G-T

103879672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487875-A-G

103879714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487916-T-C

103879752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487959-G-A

103879752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487959-G-T

103879757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487979-G-A

103879757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487979-G-C

103879757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487979-G-T

103879758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487980-A-G

103879759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487981-G-A

103879759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487981-G-T

http://identifiers.org/hco/10/GRCh38#103879765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47487987-C-A

103879765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487987-C-G

103879765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47487987-C-T

103879781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488003-G-A

103879781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488003-G-T

http://identifiers.org/hco/10/GRCh38#103879808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47488028-A-C

103879838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488063-G-A

103879838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488063-G-T

103879892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488114-G-A

103879892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488114-G-T

103879899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488126-C-T

103879906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488133-T-C

http://identifiers.org/hco/10/GRCh38#103880537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47488176-C-A

103880841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488463-G-A

103880947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488519-C-T

103881012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488591-T-C

103881085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47488656-A-G

http://identifiers.org/hco/10/GRCh38#103881236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47488789-C-A

103881545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489016-C-T

103881937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489354-T-C

103881945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489362-C-G

103881970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489387-C-T

103881975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489392-G-A

103882077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489487-G-A

103882123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489523-G-C

http://identifiers.org/hco/10/GRCh38#103882132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47489530-C-A

103882222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489621-G-A

103882243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489642-G-A

103882446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489846-A-G

103882460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489857-G-T

103882552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489905-G-A

103882552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47489905-G-T

http://identifiers.org/hco/10/GRCh38#103882604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47489940-C-A

103882604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47489940-C-T

103882633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47489967-G-A

103882633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47489967-G-T

103882710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47490025-T-C

103882738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47490053-C-T

103882804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47490119-G-A

103882804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47490119-G-C

103882846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 47490161-A-G

103882915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47490228-T-C

103883465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47490785-G-C

http://identifiers.org/hco/10/GRCh38#103884878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47491216-A-C

103886578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47491759-T-C

103886671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47491857-G-A

103886762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47491941-A-G

103887153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47492169-T-A

103887549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47492468-T-C

103887653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47492737-G-A

103887653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47492737-G-C

103888410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47495651-C-T

http://identifiers.org/hco/10/GRCh38#103888512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47495754-A-C

103888682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47495927-A-G

103888928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496133-G-A

103888928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496133-G-C

103888928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496133-G-T

103888929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496134-G-A

103888929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496134-G-T

103889044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47496221-G-T

103889204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496371-T-C

103889500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496679-C-T

103889501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496680-T-C

103889630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496791-C-T

103890080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47496996-G-C

103890140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497056-G-A

103890185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497106-A-G

103890186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497107-G-A

103890350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497203-T-C

103890356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497209-C-T

103890384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497236-G-T

103890440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497304-A-G

103890562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497484-G-A

103890735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497603-T-C

103890842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497698-G-C

103890846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497702-C-T

103890884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497721-A-T

103891055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497895-T-G

103891083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47497919-C-T

103891184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498017-A-G

103891325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498142-T-C

103891362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498175-C-G

103891363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498176-T-C

103891532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498317-A-G

103891538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498323-C-T

103892002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498671-A-G

103892032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498687-T-C

103892208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47498852-T-C

http://identifiers.org/hco/10/GRCh38#103892304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47498934-C-A

103892304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47498934-C-T

http://identifiers.org/hco/10/GRCh38#103892380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47499014-C-A

103892380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47499014-C-T

http://identifiers.org/hco/10/GRCh38#103892381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47499015-C-A

103894581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47499355-G-A

103894629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47499405-T-C

http://identifiers.org/hco/10/GRCh38#103894658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47499434-C-A

103894659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47499435-A-G

103894932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47499656-A-G

http://identifiers.org/hco/10/GRCh38#103895045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47499712-C-A

http://identifiers.org/hco/10/GRCh38#103895197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47499849-C-A

103895197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47499849-C-T

http://identifiers.org/hco/10/GRCh38#103895432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47500056-A-C

103895520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500512-A-T

103895609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500643-G-A

103895740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500769-G-A

103895742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500771-A-T

103895743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500772-T-C

103895790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500812-A-G

103895809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500831-T-C

103895907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47500942-T-G

103896017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501042-T-A

103896058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501083-C-T

103896102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501114-G-A

103896130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501134-C-T

103896310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501321-G-A

103896384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501424-C-G

103896434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47501588-C-T

103897416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502123-G-T

103897422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502129-G-T

http://identifiers.org/hco/10/GRCh38#103897467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47502172-C-A

103897467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502172-C-T

103897472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502178-G-T

103897499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502216-A-G

http://identifiers.org/hco/10/GRCh38#103897526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47502231-C-A

103897540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 47502242-G-A

http://identifiers.org/hco/10/GRCh38#103897686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47502388-C-A

103897686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47502388-C-T

103897708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47502410-G-A

103897728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502430-G-A

103897743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502446-G-A

103897743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502446-G-T

103897775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502479-T-C

103897835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502562-T-A

103897857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502584-A-T

103897923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502640-A-G

103897923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502640-A-T

103897936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502651-A-G

103898183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47502868-T-C

http://identifiers.org/hco/10/GRCh38#103898354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47504015-C-A

103898354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 47504015-C-G

http://identifiers.org/hco/10/GRCh38#103898356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47504017-C-A

103898370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 47504031-T-C

103898441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504113-T-C

103898513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504194-G-T

103898776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504460-A-G

103898776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504460-A-T

103898807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504482-A-G

103898983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47504636-C-G

103898983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47504636-C-T

http://identifiers.org/hco/10/GRCh38#103899029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47504679-C-A

103899029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504679-C-G

103899029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504679-C-T

103899048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504691-T-C

http://identifiers.org/hco/10/GRCh38#103899075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47504717-C-A

103899075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504717-C-T

103899262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47504842-G-C

103899726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505174-C-T

103899905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505315-T-C

103900207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47505611-T-C

103900235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505638-T-C

103900304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505705-T-G

http://identifiers.org/hco/10/GRCh38#103900306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47505707-A-C

103900313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505714-C-T

http://identifiers.org/hco/10/GRCh38#103900319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47505720-A-C

103900319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505720-A-G

103900336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47505727-T-C

http://identifiers.org/hco/10/GRCh38#103900368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47505759-C-A

http://identifiers.org/hco/10/GRCh38#103900723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47506982-C-A

103900845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47507061-T-C

http://identifiers.org/hco/10/GRCh38#103901045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47507269-C-A

103901114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47507337-C-T

103901228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47507447-T-C

103901256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47507475-A-G

103902125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47508752-A-G

103902126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47508753-C-T

103902188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47508805-G-A

103902207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47508825-C-T

103902208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47508826-G-A

http://identifiers.org/hco/10/GRCh38#103902234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47508846-C-A

103902386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509000-A-G

103902569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509176-T-A

http://identifiers.org/hco/10/GRCh38#103902839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47509476-C-A

103902875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509511-G-A

103902875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509511-G-T

103902995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509637-T-G

103903347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509988-C-G

103903347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47509988-C-T

103903406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47510033-T-C

http://identifiers.org/hco/10/GRCh38#103903915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47511594-C-A

103903915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511594-C-T

103904067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511740-G-A

103904067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511740-G-T

103904084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511759-G-C

103904084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511759-G-T

103904233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47511895-G-A

http://identifiers.org/hco/10/GRCh38#103904593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47512497-C-A

103904668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47512702-T-C

103904759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47512768-G-A

103904759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47512768-G-T

103904909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47512914-G-T

http://identifiers.org/hco/10/GRCh38#103904941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47512972-C-A

103905027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513081-G-C

103905027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513081-G-T

http://identifiers.org/hco/10/GRCh38#103905198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47513234-A-C

103905203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513239-G-A

103905203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513239-G-C

103905203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513239-G-T

http://identifiers.org/hco/10/GRCh38#103905250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47513309-C-A

http://identifiers.org/hco/10/GRCh38#103905398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47513421-A-C

http://identifiers.org/hco/10/GRCh38#103905890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47513866-A-C

103905890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47513866-A-G

http://identifiers.org/hco/10/GRCh38#103906196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47514144-A-C

103906491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47514360-T-C

103907312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47514457-G-C

103907409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47514603-A-G

http://identifiers.org/hco/10/GRCh38#103907418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47514612-C-A

103907457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47514651-A-G

103908173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47514897-T-C

103908241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47514959-T-G

103908266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47514984-A-T

103908377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515077-C-T

103908442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515108-G-A

103908485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515148-G-A

103908587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515216-C-T

103908676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515296-G-C

103908729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515349-A-G

103908993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47515597-T-G

103909003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515607-A-T

103909165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515790-T-C

103909186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515822-G-A

103909226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515860-T-C

103909363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515953-A-T

103909367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47515957-T-A

http://identifiers.org/hco/10/GRCh38#103909566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47515999-C-A

103909647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516076-A-G

103909746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516144-T-C

103909779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516177-G-A

103909851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516251-C-G

103909958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516485-T-C

103910012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516539-T-C

103910037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516562-T-C

103910066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516590-G-A

103910067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516591-C-T

103910104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516644-T-C

103910377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516901-G-T

103910380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516904-G-A

103910380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516904-G-T

http://identifiers.org/hco/10/GRCh38#103910381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47516905-C-A

http://identifiers.org/hco/10/GRCh38#103910383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47516907-A-C

103910384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516908-T-C

103910384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516908-T-G

103910386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516910-A-G

103910386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47516910-A-T

http://identifiers.org/hco/10/GRCh38#103910438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47517002-C-A

http://identifiers.org/hco/10/GRCh38#103910474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47517039-C-A

103910588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47517137-C-T

103910641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47517190-A-T

103910654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47517200-T-C

103910654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47517200-T-G

http://identifiers.org/hco/10/GRCh38#103910735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47517272-C-A

103910735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47517272-C-T

103911099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518170-A-G

http://identifiers.org/hco/10/GRCh38#103911100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47518171-C-A

103911199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518268-G-A

103911284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518351-G-T

103911311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518380-G-T

103911362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518446-G-T

103911386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518473-G-A

103911386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518473-G-C

103911559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518651-A-T

http://identifiers.org/hco/10/GRCh38#103911619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47518801-C-A

103911619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47518801-C-T

103912014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47519119-C-T

103913376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47519520-C-T

103913629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47519796-G-A

103913762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47519904-T-C

103914735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521388-A-T

103914754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521404-T-C

103914786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521435-T-A

103914786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521435-T-G

103914842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521474-T-C

http://identifiers.org/hco/10/GRCh38#103914859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47521491-A-C

http://identifiers.org/hco/10/GRCh38#103914936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47521571-A-C

103915033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521632-C-G

103915033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521632-C-T

http://identifiers.org/hco/10/GRCh38#103915053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47521651-C-A

103915053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47521651-C-T

103915504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47522014-G-A

103916127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47522562-G-A

103916127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47522562-G-C

103916502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47522927-T-C

103916591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47523020-T-C

103916621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47523049-T-A

103916621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47523049-T-C

103916852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524015-A-G

103916928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524077-T-A

103916928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524077-T-C

103916965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524109-T-C

103917116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524219-G-A

103917291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524470-T-A

103917291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524470-T-C

103917292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524471-G-T

103917320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524508-T-A

103917320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524508-T-G

http://identifiers.org/hco/10/GRCh38#103917383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47524557-C-A

http://identifiers.org/hco/10/GRCh38#103917440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47524611-C-A

103917440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524611-C-G

103917440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47524611-C-T

http://identifiers.org/hco/10/GRCh38#103917556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47524729-A-C

103917556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47524729-A-G

103917607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47524780-C-T

103917666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524821-A-G

103917686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524841-T-G

103917689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524844-G-A

103917689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524844-G-C

103917689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47524844-G-T

103917799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524923-G-A

103917799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524923-G-C

103917799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524923-G-T

103917800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524924-G-A

103917800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524924-G-T

103917801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524925-G-C

103917801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47524925-G-T

http://identifiers.org/hco/10/GRCh38#103918129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47525320-A-C

103918129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47525320-A-G

103918129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47525320-A-T

http://identifiers.org/hco/10/GRCh38#103918134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47525325-C-A

103918134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47525325-C-T

103918140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47525346-G-A

103918140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47525346-G-C

103918140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47525346-G-T

103918198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47525433-G-T

103918297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47525513-T-A

103918297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47525513-T-C

103918297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26200
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47525513-T-G