http://identifiers.org/hco/2/GRCh38#28392476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32292798-C-A

28392476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32292798-C-T

28392558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292881-T-A

28392613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292936-G-A

28392613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292936-G-C

28392613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292936-G-T

28392644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292967-G-A

28392644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292967-G-T

http://identifiers.org/hco/2/GRCh38#28392648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32292971-C-A

28392648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292971-C-T

28392650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292973-C-T

28392697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32293019-G-A

28392893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293229-G-A

28392893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293229-G-C

28392979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293317-C-T

28393308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293646-G-T

http://identifiers.org/hco/2/GRCh38#28393398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32293734-C-A

28393398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293734-C-T

http://identifiers.org/hco/2/GRCh38#28393636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32293964-C-A

28393636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32293964-C-T

http://identifiers.org/hco/2/GRCh38#28393865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32294192-C-A

http://identifiers.org/hco/2/GRCh38#28393869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32294196-C-A

28393869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294196-C-T

28393878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294205-G-A

28393878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294205-G-C

28393878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294205-G-T

28393906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294240-C-T

28393958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294292-T-C

http://identifiers.org/hco/2/GRCh38#28394144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32294512-C-A

28394144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294512-C-G

28394285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294664-A-G

28394285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294664-A-T

http://identifiers.org/hco/2/GRCh38#28394410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32294787-C-A

28394410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32294787-C-T

http://identifiers.org/hco/2/GRCh38#28394512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32294868-C-A

28394566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32294921-C-T

28394600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32294947-A-G

http://identifiers.org/hco/2/GRCh38#28394695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32295041-C-A

28394754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295100-C-G

28394754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295100-C-T

28394781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295125-T-A

28394781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295125-T-C

28394781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295125-T-G

28395001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295367-G-C

28395001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295367-G-T

28395041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295407-C-T

28395278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295644-C-T

28395523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32295877-G-A

28395523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32295877-G-T

http://identifiers.org/hco/2/GRCh38#28395701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32296055-C-A

28395701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32296055-C-T

28395830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296170-G-T

28395844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296183-C-T

28395850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296189-G-T

http://identifiers.org/hco/2/GRCh38#28395899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32296238-C-A

28396094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296428-A-G

28396221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296566-C-T

28396232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296577-T-C

28396349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296709-G-C

28396957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32297299-C-T

28396982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32297324-A-T

28397112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32297452-T-A

28397357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297617-G-A

28397466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297721-T-C

28397557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297805-C-T

28397678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297991-T-C

http://identifiers.org/hco/2/GRCh38#28397788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32298114-A-C

28397788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298114-A-G

28397919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298251-C-T

28398132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298429-G-A

28398151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298445-A-G

28398154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298448-A-G

28398182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298476-T-C

28398257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298545-G-A

28398383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298628-A-T

28398407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298652-G-A

28398437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298707-T-C

28398477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298785-C-G

28398517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298824-C-T

28398919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299174-T-C

28399004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299246-A-G

28399116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299349-C-T

28399291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299490-C-T

http://identifiers.org/hco/2/GRCh38#28399393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32299590-A-C

http://identifiers.org/hco/2/GRCh38#28399433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32299630-A-C

28399433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299630-A-G

28399974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300050-G-A

http://identifiers.org/hco/2/GRCh38#28400049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32300117-C-A

28400222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300297-G-A

28400446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300526-C-T

28400529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300594-T-C

28400759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300822-C-T

28400904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300939-G-A

28400945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300977-G-A

28401313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301370-A-G

28401412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301457-T-C

28402591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32302268-A-G

28403099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32302720-C-G

28403519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303582-C-T

28403883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303958-G-T

28403891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303966-G-A

28403975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304049-G-A

28403975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304049-G-T

28404365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32304427-C-G

28404487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304485-A-G

28404706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304631-A-G

28405389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305003-G-C

28405556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305156-C-T

28405601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305210-G-A

28405652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305258-G-A

28405781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305366-C-T

28405787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305372-T-C

28406018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305576-A-G

28406018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32305576-A-T

28406840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306006-G-A

http://identifiers.org/hco/2/GRCh38#28407154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32306290-C-A

28407493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306554-T-C

28407670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306705-C-T

28407671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306706-C-T

28408108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307010-T-C

28408326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307245-G-A

28408424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307475-C-G

28408560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307601-C-T

28408561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307602-A-T

28408605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307645-C-T

http://identifiers.org/hco/2/GRCh38#28408611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32307651-C-A

28408611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307651-C-T

http://identifiers.org/hco/2/GRCh38#28408715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32307725-C-A

28408715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307725-C-G

28408715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307725-C-T

28408727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307737-T-C

28408735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307745-A-G

28408842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: synonymous variant
orthologous variants: 32307848-G-A

28408890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32307894-G-A

http://identifiers.org/hco/2/GRCh38#28408984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32307928-C-A

28408984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32307928-C-T

28409069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308049-T-C

28409077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308057-G-C

http://identifiers.org/hco/2/GRCh38#28409422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32308253-C-A

28409961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308619-G-A

28410246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308723-A-G

28410250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308727-C-T

28410351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308835-C-T

28410380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308864-C-T

28410415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308890-C-G

28410415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308890-C-T

http://identifiers.org/hco/2/GRCh38#28410419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32308894-C-A

28410419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308894-C-T

28410427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308902-G-A

28410427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308902-G-C

28410427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32308902-G-T

http://identifiers.org/hco/2/GRCh38#28410436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32308911-C-A

28410466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32308940-T-A

28410466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32308940-T-C

28410496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32308958-G-A

28410510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, missense_variant
orthologous variants: 32308972-T-C

28410510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, missense_variant
orthologous variants: 32308972-T-G

28410520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32308982-G-A

28410625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309094-G-A

28410815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309276-C-T

28411005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309393-G-A

28411005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309393-G-C

28411340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309470-G-A

28411755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309836-A-G

28411761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309842-G-T

28411762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309843-G-A

28411762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309843-G-T

28411765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309844-T-C

28411845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron variant
orthologous variants: 32309917-T-C

http://identifiers.org/hco/2/GRCh38#28411908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32309994-C-A

28411908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32309994-C-T

28412017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310102-T-C

http://identifiers.org/hco/2/GRCh38#28412034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32310119-A-C

28412034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310119-A-T

28412103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310188-G-C

28412103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310188-G-T

28412136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32310221-G-T

28412145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310230-G-T

28412277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32310362-A-G

28412347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32310432-G-A

28412347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32310432-G-T

http://identifiers.org/hco/2/GRCh38#28412498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32310588-C-A

28412498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32310588-C-T

http://identifiers.org/hco/2/GRCh38#28412725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32310824-A-C

28412725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32310824-A-G

28412807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32310912-G-A

28412807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32310912-G-C

28412807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32310912-G-T

http://identifiers.org/hco/2/GRCh38#28412822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32310927-A-C

28413035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311141-C-T

28413206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311309-T-A

http://identifiers.org/hco/2/GRCh38#28413288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32311392-C-A

28413360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311454-T-C

http://identifiers.org/hco/2/GRCh38#28413408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32311502-C-A

28413585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311586-G-A

28413585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311586-G-T

28413617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311619-G-A

28413617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311619-G-T

http://identifiers.org/hco/2/GRCh38#28413661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32311660-C-A

28413670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311669-G-A

28413670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311669-G-T

28413675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311674-G-A

28413675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311674-G-C

http://identifiers.org/hco/2/GRCh38#28413770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32311768-C-A

28413770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311768-C-T

28413796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311772-G-A

28413796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311772-G-T

28413917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311886-C-G

28413917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311886-C-T

28413976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311927-G-A

28413976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32311927-G-T

28414110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312020-T-C

28414125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312035-G-T

http://identifiers.org/hco/2/GRCh38#28414126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32312036-C-A

28414126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312036-C-T

28414201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312111-C-T

28414219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312129-C-G

28414219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312129-C-T

28414282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312188-C-T

28414510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312389-G-T

28414519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312398-A-T

28414655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312516-T-C

28414849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312686-A-G

http://identifiers.org/hco/2/GRCh38#28414990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32312820-C-A

28415095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312942-T-A

28415131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312961-G-A

28415150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312972-G-A

28415150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32312972-G-T

28415204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313025-G-A

28415204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313025-G-T

28415218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313039-C-T

28415392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313204-G-T

28415398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313210-T-C

http://identifiers.org/hco/2/GRCh38#28415422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32313233-C-A

28415434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313261-G-A

28415434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313261-G-T

http://identifiers.org/hco/2/GRCh38#28415470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32313292-C-A

28415470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313292-C-G

28415470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313292-C-T

28415502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313319-T-C

http://identifiers.org/hco/2/GRCh38#28415510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32313327-A-C

28415510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313327-A-G

28415510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313327-A-T

28415617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313444-T-C

28415687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313514-G-A

28415687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313514-G-T

28415892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313707-T-A

28415892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313707-T-C

28415892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313707-T-G

28416138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32313995-A-G

http://identifiers.org/hco/2/GRCh38#28416171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32314031-C-A

28416171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32314031-C-T

28416215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32314076-G-T

28416216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32314077-G-A

28416674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32314554-A-T

28416921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32314792-A-G

28417245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32315118-G-A

28417245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3798
most severe consequence: 3 prime UTR variant
orthologous variants: 32315118-G-T