http://identifiers.org/hco/7/GRCh38#47795541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8784377-A-C

47795541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784377-A-G

47795541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784377-A-T

47795613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784445-T-G

47795618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784450-C-T

47795658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8784490-C-G

http://identifiers.org/hco/7/GRCh38#47795837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#8784645-C-A

47795837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8784645-C-T

http://identifiers.org/hco/7/GRCh38#47795864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#8784673-C-A

47795864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8784673-C-T

47795989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 8784774-G-A

47796064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8784846-A-G

http://identifiers.org/hco/7/GRCh38#47796096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#8784878-A-C

47796096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8784878-A-G

http://identifiers.org/hco/7/GRCh38#47796261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8785040-C-A

47796261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8785040-C-T

http://identifiers.org/hco/7/GRCh38#47800353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8785939-A-C

http://identifiers.org/hco/7/GRCh38#47800547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8786098-C-A

47800547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786098-C-T

47800705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786259-T-C

47800707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786261-G-T

47800710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786264-C-G

47800710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786264-C-T

47800724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786278-G-A

47800739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786293-G-A

47800739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786293-G-C

47800739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8786293-G-T

http://identifiers.org/hco/7/GRCh38#47800895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8786449-C-A

47800895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786449-C-G

http://identifiers.org/hco/7/GRCh38#47800916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8786469-A-C

47800935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786488-A-G

47802392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793453-A-G

47802451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793508-C-T

47802489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793546-C-T

47802524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793581-G-A

47802559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793626-C-T

47802581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793648-C-T

47802636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793725-G-C

47802670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793759-C-T

47802752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793837-C-T

http://identifiers.org/hco/7/GRCh38#47802822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8794163-A-C

47802852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794195-G-A

47802853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794196-C-T

http://identifiers.org/hco/7/GRCh38#47802872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8794214-C-A

47802872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794214-C-T

47802873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794215-G-A

47803050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794386-A-G

47803087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794422-A-G

47803091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794426-T-C

47803103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794438-C-T

47803200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794530-G-A

47803200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794530-G-T

47803230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8794552-G-A

47803336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8794658-T-G

47803437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794765-T-A

47803437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794765-T-C

47803471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794792-T-C

47803700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794956-C-T

47803859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795059-T-C

47803998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795180-T-C

47804149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795324-A-G

47806237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8796837-C-G

47806586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797077-T-C

http://identifiers.org/hco/7/GRCh38#47806625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8797114-C-A

47806823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797247-G-A

47806823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797247-G-C

47806823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797247-G-T

47806826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797250-C-T

47806827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797251-G-A

47807842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798545-G-A

47807997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8798680-C-T

http://identifiers.org/hco/7/GRCh38#47808095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8798770-C-A

47808095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798770-C-G

47808095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798770-C-T

47808101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798776-A-G

47808101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798776-A-T

47808120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798795-G-A

47808120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798795-G-C

47808120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798795-G-T

http://identifiers.org/hco/7/GRCh38#47808126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8798801-C-A

47808126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798801-C-T

47808170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8798840-G-A

47808269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8798940-G-A

47808313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8798984-A-G

47808323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8798994-C-G

47808366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8799037-G-A

47808411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799082-C-T

47808418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799089-G-A

47808440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799113-T-C

47809394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8799569-T-C

47809535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8799717-G-A

47809556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8799738-G-T

47809557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8799739-G-A

47809557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8799739-G-C

47809583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8799763-G-A

47809583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8799763-G-T

47809584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8799764-G-T

http://identifiers.org/hco/7/GRCh38#47809646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8799826-C-A

47809646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799826-C-T

47809694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8799868-G-T

47809830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800008-C-T

47810311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800385-G-A

47810427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800501-C-T

47810431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800513-T-A

47810488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800562-T-A

47810764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800766-G-A

47810793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800793-T-G

47810892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800880-A-G

47810905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800890-G-C

47810929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800914-A-T

47810932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800918-T-G

47810934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800920-G-A

47810934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800920-G-C

47810948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800938-T-C

http://identifiers.org/hco/7/GRCh38#47810955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8800945-A-C

47810998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800983-T-C

47811584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804127-T-C

47811626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804161-G-T

47811669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804207-G-A

47811669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804207-G-C

47811669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804207-G-T

47811675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804213-A-G

47811682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804220-G-C

47811682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804220-G-T

47811766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804294-G-A

47811766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804294-G-T

47811994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8804520-G-A

47811994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8804520-G-T

47812009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8804535-C-T

http://identifiers.org/hco/7/GRCh38#47812098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8804621-A-C

47812110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804634-T-C

47812112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804636-A-G

http://identifiers.org/hco/7/GRCh38#47812147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8804670-C-A

47812147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804670-C-T

47812176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804697-G-T

47812202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804720-T-C

47812202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804720-T-G

47812267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804773-C-T

47812342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804834-T-C

47812342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8804834-T-G

47812718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805187-C-T

47812939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805409-G-C

47813012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805481-G-T

47813257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8805675-T-C

47813257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8805675-T-G

47813403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805821-A-G

http://identifiers.org/hco/7/GRCh38#47813407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8805825-C-A

47813407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8805825-C-T

http://identifiers.org/hco/7/GRCh38#47813540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8805955-C-A

47813540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8805955-C-T

47813568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8805981-A-G

http://identifiers.org/hco/7/GRCh38#47813594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806005-C-A

47813594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806005-C-T

47813616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806027-T-C

47813802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806176-A-G

47813802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806176-A-T

47813880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806233-C-T

47813974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8806303-G-T

47814023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806352-A-G

47814081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806399-G-A

47814081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806399-G-T

47814086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806404-A-G

http://identifiers.org/hco/7/GRCh38#47814091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806409-C-A

47814091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806409-C-T

http://identifiers.org/hco/7/GRCh38#47814121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806434-C-A

47814147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806459-T-A

47814147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806459-T-C

http://identifiers.org/hco/7/GRCh38#47814148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806460-C-A

http://identifiers.org/hco/7/GRCh38#47814150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806462-A-C

47814941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8806759-G-T

http://identifiers.org/hco/7/GRCh38#47815083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#8806863-A-C

47815169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8806925-G-T

47815182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8806938-T-C

47815224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8806957-G-T

47815280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8806999-T-C

47815330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807032-T-C

47815401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807100-C-T

47815489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807187-T-A

47815489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807187-T-C

47815489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807187-T-G

47815496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807194-C-T

47815572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807249-T-A

47815572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807249-T-C

47815592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807268-T-A

47815592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807268-T-C

47815592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807268-T-G

http://identifiers.org/hco/7/GRCh38#47815608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8807284-C-A

47815608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807284-C-T

47815664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807334-G-A

47815664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807334-G-T

47818064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8808447-C-T

47818071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8808454-T-C

http://identifiers.org/hco/7/GRCh38#47818080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808463-A-C

http://identifiers.org/hco/7/GRCh38#47818096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808480-C-A

47818096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8808480-C-T

47818126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8808511-G-T

47818198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808573-G-A

47818218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808593-A-G

http://identifiers.org/hco/7/GRCh38#47818229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808604-A-C

http://identifiers.org/hco/7/GRCh38#47818248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808623-C-A

47818248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808623-C-T

http://identifiers.org/hco/7/GRCh38#47818259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808633-A-C

47818259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808633-A-G

47818281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808646-G-C

http://identifiers.org/hco/7/GRCh38#47818294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8808659-A-C

47818294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8808659-A-G

47818631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809278-G-A

47818678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809325-G-A

47818802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809411-T-C

47818872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809472-T-C

http://identifiers.org/hco/7/GRCh38#47818928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8809544-C-A

47818958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809566-G-A

47818958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809566-G-T

47818959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809567-A-G

http://identifiers.org/hco/7/GRCh38#47819003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8809611-C-A

47819003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8809611-C-T

47819529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810085-T-C

http://identifiers.org/hco/7/GRCh38#47819717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#8810240-C-A

47819731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8810254-G-A

47819731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21911
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8810254-G-T