92836572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3391487-A-G

http://identifiers.org/hco/7/GRCh38#92836592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#3391467-A-C

92836697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391365-C-T

92836791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3391294-C-T

92836871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391251-C-T

92836912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391213-C-T

92836914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391211-T-C

http://identifiers.org/hco/7/GRCh38#92836935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3391190-A-C

92836935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391190-A-G

92836937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391188-G-A

92837015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391126-T-C

92837015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391126-T-G

92837032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391108-G-T

http://identifiers.org/hco/7/GRCh38#92837034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3391106-A-C

92837054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391086-C-T

92837060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391080-G-A

92837065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3391075-G-C

92837161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390960-A-G

92837189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390936-T-C

92837224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390905-T-C

92837307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390830-A-G

92837321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390816-C-T

92837377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390760-T-C

92837413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390723-T-C

92837423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390713-A-G

92837461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390675-G-A

http://identifiers.org/hco/7/GRCh38#92838113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3390034-C-A

92838137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3390010-G-A

http://identifiers.org/hco/7/GRCh38#92838245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3389910-A-C

92838245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389910-A-G

http://identifiers.org/hco/7/GRCh38#92838250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3389906-C-A

92838317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389860-A-G

92838430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389752-T-A

92838686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389484-T-C

92838971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389199-G-A

92838971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389199-G-T

92838993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389177-T-C

http://identifiers.org/hco/7/GRCh38#92839059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3389107-A-C

92839059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3389107-A-G

92839301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3388887-A-G

http://identifiers.org/hco/7/GRCh38#92839427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3388711-C-A

92840299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3388066-C-T

92840469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3387910-C-T

92840506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3387873-C-T

92840523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3387856-T-G

92840618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3387762-A-G

92840644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3387736-G-A

92841028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386978-C-T

92841029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386977-G-A

92841029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386977-G-C

92841043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386963-A-G

http://identifiers.org/hco/7/GRCh38#92841071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3386935-A-C

92841071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386935-A-G

92841081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386924-C-T

92841246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386748-C-T

92841318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386685-A-G

92841386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386614-G-A

92841386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386614-G-C

92841434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386565-T-C

92841676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386392-G-C

92841709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386359-A-G

92841778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386298-A-G

92841793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386283-G-A

92841870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386209-T-C

92841918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386163-C-T

92842069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386016-G-A

92842089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3386001-G-A

92842113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385978-T-C

92842178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385920-A-G

92842189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385909-C-T

92842276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385818-T-C

92842322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385772-T-C

92842454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385650-T-A

92842515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385595-T-C

92842521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385589-A-T

http://identifiers.org/hco/7/GRCh38#92842544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3385566-C-A

92842551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385559-A-G

http://identifiers.org/hco/7/GRCh38#92842577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3385533-C-A

92842709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385412-T-A

92842789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385312-A-G

92842789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385312-A-T

92842861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385241-G-C

92842861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385241-G-T

92842927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385207-C-G

http://identifiers.org/hco/7/GRCh38#92842932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3385202-C-A

92842966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385167-A-G

92842969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385164-A-G

92843042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385091-A-G

92843084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385050-A-G

92843107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385027-G-A

92843107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385027-G-T

92843119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3385015-A-T

92843162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384974-T-C

http://identifiers.org/hco/7/GRCh38#92843244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3384894-A-C

92843342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384816-T-C

92843414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384756-C-T

92843568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384631-G-A

92843589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384595-C-T

92843652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384520-G-A

92843746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384473-T-C

92843981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384245-T-C

92843991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384235-T-C

92844134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3384032-G-T

92844171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383997-C-T

92844206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383965-G-C

92844239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383942-A-G

92844239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383942-A-T

92844258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383926-A-G

92844289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383895-T-C

92844353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383828-G-C

92844387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383793-C-G

92844435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383747-G-A

92844559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383658-C-T

92844582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383635-A-G

92844592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383625-C-T

92844648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383569-A-G

92844670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383547-C-T

http://identifiers.org/hco/7/GRCh38#92844673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3383545-C-A

92844673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383545-C-T

92845681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383341-C-T

92845727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383295-G-A

92845827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383197-A-G

92845938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383090-T-G

92845992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3383042-G-A

92846058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3382943-T-C

http://identifiers.org/hco/7/GRCh38#92846085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3382916-A-C

http://identifiers.org/hco/7/GRCh38#92846131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3382866-A-C

92846215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3382753-G-A

92846290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3382605-C-T

92846513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3382244-G-T

92846592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3382112-A-T

92847202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3381608-A-G

http://identifiers.org/hco/7/GRCh38#92847249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3381556-C-A

92847249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3381556-C-G

92847715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3381231-A-G

92847815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3381111-T-C

http://identifiers.org/hco/7/GRCh38#92847846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3381090-C-A

92847899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3381046-T-A

92848440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3380550-T-C

http://identifiers.org/hco/7/GRCh38#92848770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3380139-C-A

92848770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3380139-C-T

92849051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379952-A-G

92849110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379895-C-T

92849420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379602-G-A

92849477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379545-G-C

92849673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379367-C-T

92849689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379351-C-T

92849877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3379210-A-G

92850180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3378621-T-G

92850604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3378015-C-T

92850659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377963-G-A

92850772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377853-G-C

92851119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377483-A-G

92852651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377317-G-A

92852714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377254-T-A

92852746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377223-T-A

92852746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377223-T-G

92852830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377145-A-G

92852851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3377121-C-T

92853069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376515-A-G

92853077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376507-C-T

92853156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376425-T-C

92853165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376416-T-A

92853239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376343-A-G

92853312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376284-C-T

92853321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376273-T-C

92853425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376185-T-C

92853447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3376163-A-G

92853978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3375676-T-C

92854341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3375372-G-A

92854575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3375148-C-T

92854718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3375030-G-A

http://identifiers.org/hco/7/GRCh38#92855149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3366573-C-A

http://identifiers.org/hco/7/GRCh38#92855220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3366509-C-A

92855297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3366441-G-A

92855629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3366101-G-A

92855655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3365268-G-C

92855679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3365245-A-G

92855722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3365223-G-A

92855722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3365223-G-T

http://identifiers.org/hco/7/GRCh38#92855771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3365182-C-A

http://identifiers.org/hco/7/GRCh38#92855917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3365069-C-A

http://identifiers.org/hco/7/GRCh38#92855933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3365053-C-A

92867203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3362440-T-G

92867209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3362434-G-A

92867365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3362317-T-C

92867386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3362297-A-G

http://identifiers.org/hco/7/GRCh38#92868221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3361744-A-C

92868397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3361602-C-T

92868669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3361354-T-C

92872844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3359766-T-A

92873913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3358850-A-T

92874362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3358418-T-A

92874366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3358414-A-G

92874482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3358325-G-A

92874727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3358013-C-T

92874942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3357406-T-C

92903647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3351942-C-G

92903651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3351938-A-G

92904287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3351512-A-G

92904301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3351498-T-A

92904755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3351073-T-C

92904760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3351068-T-C

92904781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3351050-C-G

92915639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3341302-G-A

92915943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3341166-C-T

92915965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3341151-A-G

92916068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3341047-G-A

92916083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3341032-A-G

92916135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3340982-A-T

92916326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3340801-A-G

http://identifiers.org/hco/7/GRCh38#92916408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3340702-A-C

92916562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3340567-T-C

92916600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3340529-C-T

92916816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3340348-G-C

92916816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3340348-G-T

92917135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 3340030-G-A

92917135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 3340030-G-T

92917138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40141
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 3340027-A-G