38556813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158884-G-A

38556813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158884-G-T

38556868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158832-C-T

38556896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158804-A-G

38556908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7158792-G-T

38556916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7158784-G-C

38556916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7158784-G-T

http://identifiers.org/hco/5/GRCh38#38556951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7158749-C-A

38556951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158749-C-T

38556957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158743-G-T

38556994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158703-A-G

38556994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158703-A-T

http://identifiers.org/hco/5/GRCh38#38557049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7158659-C-A

38557153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158555-A-G

http://identifiers.org/hco/5/GRCh38#38557158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7158550-C-A

38557158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158550-C-T

38557210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158500-A-G

38557210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158500-A-T

38557267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158442-G-A

38557267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158442-G-C

38557267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158442-G-T

38557495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7158214-G-A

38557627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7158086-T-C

http://identifiers.org/hco/5/GRCh38#38557770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7157925-C-A

38557770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157925-C-G

38557844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157863-G-A

38557844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157863-G-T

38557853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157854-T-C

38557856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157851-A-G

http://identifiers.org/hco/5/GRCh38#38558097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7157630-C-A

38558140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157595-T-A

38558231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157527-G-A

38558349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157391-G-T

38558462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157333-A-G

38558478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157317-C-G

http://identifiers.org/hco/5/GRCh38#38558504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7157291-A-C

38558504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157291-A-G

38558504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157291-A-T

38559094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157056-A-T

http://identifiers.org/hco/5/GRCh38#38559157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7157002-C-A

38559157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157002-C-G

38559157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7157002-C-T

38559756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156384-G-A

38559796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156356-C-T

38559821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156331-G-A

38559821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156331-G-C

38559821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156331-G-T

38559824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156328-T-C

38559824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156328-T-G

38559833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156319-C-G

http://identifiers.org/hco/5/GRCh38#38560067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7156061-C-A

38560229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155900-A-G

38560648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155453-G-A

38561080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155314-G-A

http://identifiers.org/hco/5/GRCh38#38561159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7155237-A-C

38561586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154901-C-T

38561614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154873-T-C

38561828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154624-C-T

38562286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154094-C-T

38562799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153566-A-G

38563207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153172-G-A

38563419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153036-C-T

38563498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152971-C-G

38563510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152959-G-A

38563557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152915-G-A

38563559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152913-C-T

38563653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152790-C-T

38563716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152739-A-T

38564585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7151293-A-G

38565197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7151029-C-T

38565529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150825-G-C

38565537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150817-A-G

38566952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150508-G-A

38567212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7150363-G-A

38567496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150119-G-T

38567647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150035-G-A

38568049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149655-T-C

38568154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149548-A-G

38568325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149408-G-A

38568341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149392-G-A

38568358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149375-G-C

38568390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149342-G-T

http://identifiers.org/hco/5/GRCh38#38568600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7149141-C-A

38568855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148812-A-G

38568961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148670-A-G

38568998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148633-T-C

38569022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148608-G-T

38569136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148480-A-G

38569232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148382-T-C

38569809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148152-T-G

38570047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147935-C-T

38570156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147833-A-G

38570219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147790-G-C

38570386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147629-G-T

38570460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147554-G-A

38570583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147431-T-G

38570926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147052-A-G

38570929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7147049-A-G

38571008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146966-T-A

38571027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146949-A-G

38571063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146913-A-G

38571179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146800-T-A

http://identifiers.org/hco/5/GRCh38#38571251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7146733-C-A

38571600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146684-T-C

38571639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146650-A-G

38571828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146458-C-T

38571829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146457-A-G

http://identifiers.org/hco/5/GRCh38#38571855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7146432-A-C

38571855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146432-A-G

http://identifiers.org/hco/5/GRCh38#38571862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7146425-C-A

38571862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146425-C-T

38572002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146254-T-G

38572070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146184-G-A

38572070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146184-G-C

38572932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146072-A-G

http://identifiers.org/hco/5/GRCh38#38573102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7145904-A-C

38573298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145743-G-C

38573337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145704-T-G

38573472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145580-T-C

38573583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145487-G-A

http://identifiers.org/hco/5/GRCh38#38573677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7145398-C-A

38573684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145391-G-A

38573843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145272-G-T

38574349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7144949-C-T

38576565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142245-C-T

38576699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142097-G-C

38576926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141861-C-T

38576963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141825-A-G

38577125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141662-G-A

38577445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7140527-T-G

38579161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138821-T-C

http://identifiers.org/hco/5/GRCh38#38579169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7138813-C-A

38579169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138813-C-G

38579184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138786-G-T

38579201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138767-A-G

38579474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138549-A-G

38579500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138523-A-G

38579500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7138523-A-T

38580120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137901-G-A

38581038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7136055-A-G

38581134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135954-A-T

38581209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135880-T-A

38581259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135833-C-T

38581406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135521-C-G

38581412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135515-A-G

38581703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135219-T-C

38581789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135126-G-A

38581832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135083-A-G

38581925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135009-T-G

38582077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134888-T-G

38582354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134726-A-T

http://identifiers.org/hco/5/GRCh38#38582416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7134663-A-C

38582416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134663-A-G

http://identifiers.org/hco/5/GRCh38#38582512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7134560-C-A

38582533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134542-T-C

38582633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134443-C-G

38582761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134293-C-T

38583338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133541-A-G

38583523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133356-G-A

38583591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133290-T-C

38583651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133249-C-G

38584277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133043-A-T

38584326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132996-G-A

http://identifiers.org/hco/5/GRCh38#38584374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7132960-A-C

38584440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132892-A-T

38584624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132752-A-G

http://identifiers.org/hco/5/GRCh38#38584628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7132748-C-A

38584628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132748-C-T

38584689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132687-C-T

38584733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132631-A-G

38585303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131885-C-T

38585363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131815-C-G

38585515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131656-T-C

38585855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131398-T-G

38585868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131386-G-T

38586235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7130690-T-A

38586294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7130629-T-C

http://identifiers.org/hco/5/GRCh38#38586545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7130030-C-A

38586704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129891-G-A

38586794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129801-C-T

38586906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129693-G-A

38586956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129622-G-A

38586988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129596-C-G

38587198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129409-A-G

38587207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129400-A-G

38587329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129289-T-C

38587358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129261-C-T

38587363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129256-A-G

38587392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128094-G-T

38587406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128080-G-A

38587476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128027-G-A

38587620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127903-G-T

38587717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127829-G-A

38587724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127822-G-T

http://identifiers.org/hco/5/GRCh38#38588474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7126380-A-C

38588524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7126327-C-T

38588839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125605-T-C

38590033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124290-A-G

38590065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124262-C-T

38590213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124111-T-A

38590312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124024-G-A

38590312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124024-G-T

http://identifiers.org/hco/5/GRCh38#38591098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7122370-A-C

38591104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122364-A-T

38591107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122361-T-C

38591284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122226-T-C

38591322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122188-A-G

38591490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122058-A-T

38591826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121701-T-C

38591830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121692-T-A

38592044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121524-C-T

38592054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121514-T-C

38592256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121319-G-T

38594292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121108-G-A

38594292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121108-G-C

38594553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120880-G-T

38594741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120699-C-T

http://identifiers.org/hco/5/GRCh38#38594816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7120630-C-A

38594816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120630-C-G

38594816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120630-C-T

http://identifiers.org/hco/5/GRCh38#38594851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7120597-C-A

38594851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120597-C-G

38594851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120597-C-T

38594906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120541-T-C

38594960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120486-T-G

38595020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120421-G-T

38595071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, splice_region_variant
orthologous variants: 7120372-T-C

38595077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7120369-C-G

http://identifiers.org/hco/5/GRCh38#38595092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7120359-C-A

38595092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120359-C-G

38595092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120359-C-T

38595158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120290-G-A

38595158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120290-G-C

38595158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120290-G-T

38595165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120283-A-T

http://identifiers.org/hco/5/GRCh38#38595297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7120196-C-A

38595314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120179-G-A

38595314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120179-G-T

38595399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120098-A-G

38595429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7120068-A-T

http://identifiers.org/hco/5/GRCh38#38595452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7120049-C-A

38596912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118549-G-A

38597111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118350-G-C

38597174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118286-G-A

38597403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118052-C-T

38598800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7117163-A-G

38598915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7117050-G-T

38599055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116918-A-T

38600434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116704-A-G

38600474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116670-C-T

38600572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116570-T-G

38600989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7116192-C-T

38601008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7116173-A-G

http://identifiers.org/hco/5/GRCh38#38601121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7116085-A-C

38601121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7116085-A-G

38601143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7116065-A-G

38601143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7116065-A-T

38602094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7115134-T-G

38602221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115010-G-A

38602243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114988-G-T

38604128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114690-G-A

38604186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114636-C-T

38604194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114628-G-A

38604216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114620-G-A

38606752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112575-C-T

38606756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112571-C-T

38606806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112528-A-G

38607532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111744-C-G

38607550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111726-C-T

38607597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 7111678-T-C

http://identifiers.org/hco/5/GRCh38#38607645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7111628-C-A

http://identifiers.org/hco/5/GRCh38#38607668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7111609-C-A

38607686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111591-G-T

38607689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111588-G-A

38607689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111588-G-T

38607694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111583-A-G

38607752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111522-T-C

38607755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111519-G-C

38607755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111519-G-T

http://identifiers.org/hco/5/GRCh38#38607795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7111480-C-A

38607802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111473-G-T

38607838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111437-A-G

38607975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111092-T-C

http://identifiers.org/hco/5/GRCh38#38607985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7111082-A-C

38608015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7111052-C-T

38608068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110996-T-C

38608071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110993-G-A

38608126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110942-A-G

38608264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7110825-T-A

38608272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7110817-T-C

38608435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110618-A-G

38608488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110564-C-G

38608585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110473-A-G

38608585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110473-A-T

38608627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110432-G-A

38608757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7110249-T-C

38609064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109828-C-T

http://identifiers.org/hco/5/GRCh38#38609079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7109813-C-A

38610731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7108020-C-T

38610914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107864-G-A

38610914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107864-G-T

38610943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107843-T-C

38611008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107784-T-C

38611019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107773-T-A

38611179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107603-A-G

38611190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107592-C-T

38612244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107078-G-C

38612244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107078-G-T

38612345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106971-C-T

38612390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106920-G-C

http://identifiers.org/hco/5/GRCh38#38612492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7106823-A-C

38612778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106557-T-G

http://identifiers.org/hco/5/GRCh38#38612815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7106527-C-A

38612866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106472-A-G

38613149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106194-C-T

38613236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106126-C-T

38613284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106075-G-T

38613319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106040-G-C

38613342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106037-A-G

http://identifiers.org/hco/5/GRCh38#38613388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7105994-C-A

38613414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105968-T-C

http://identifiers.org/hco/5/GRCh38#38613472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7105907-A-C

38613496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105883-C-T

38613506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105872-C-T

38613523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105855-G-A

38613687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105693-C-G

38613729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105652-A-G

38613923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105459-C-T

38614117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7105082-C-T

http://identifiers.org/hco/5/GRCh38#38614141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7105058-A-C

38614193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105006-G-A

38614193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105006-G-C

38614197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105002-G-A

38614505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104706-C-T

38614510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104701-A-G

38614781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104567-C-T

38615115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104260-T-A

38615181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104194-G-A

38615198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104177-C-T

38615379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104063-G-A

38615415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104020-T-C

38615416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104019-G-C

38615517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103919-T-C

38615537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103899-G-A

38615553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103883-G-A

38615682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7103808-C-G

38615682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7103808-C-T

38615685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7103805-G-C

38615792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103712-G-A

38615916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103604-A-G

38616177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102853-A-T

38616196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102836-A-G

38616232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102786-G-A

38616255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102752-G-C

38616329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102678-T-C

38616399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102609-A-G

38616419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102583-T-C

38616422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102580-A-T

38621460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7101271-C-T

38621477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7101253-C-T

38621570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7101166-G-C

38621571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7101165-G-C

38621572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7101164-G-A

38621799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100993-G-A

38622178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100674-C-T

38622195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100657-C-G

38622639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100199-C-T

38622652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100186-G-A

38622655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100183-C-G

http://identifiers.org/hco/5/GRCh38#38623128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7099753-A-C

38623128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099753-A-G

38623146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099739-C-T

38623322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099574-C-T

38623400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099516-A-G

http://identifiers.org/hco/5/GRCh38#38623530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7099393-A-C

38623530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099393-A-G

38639327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096768-T-A

38639327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096768-T-C

38639852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096176-G-A

38640242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095781-T-G

38640308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095656-G-A

38640308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095656-G-T

38640334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095610-A-G

38640783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095160-A-G

http://identifiers.org/hco/5/GRCh38#38640816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7095129-C-A

http://identifiers.org/hco/5/GRCh38#38640851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7095102-A-C

38640864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095089-C-G

38640902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095068-T-G

38640967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7095003-A-G

38641043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7094929-C-T

38641094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7094879-A-G

38641106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7094867-G-A

38641129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7094844-G-A

http://identifiers.org/hco/5/GRCh38#38641883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7094274-C-A

38641883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094274-C-T

38641894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094263-A-G

38641946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094214-A-T

38642009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094164-A-G

38642097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094076-A-G

38642122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093622-T-G

38642131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093613-G-A

38642331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093419-G-C

38642390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093381-C-T

38642475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092043-T-C

38642721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091790-T-C

38642753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091758-T-A

38642850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091656-T-G

38647818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7091002-G-A

38648071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090727-T-C

38648075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090723-A-G

38648450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090455-G-A

38648696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090428-G-A

38649050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090069-G-A

38649050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090069-G-T

38649425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089703-T-C

38650787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086878-G-A

38650787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086878-G-T

38651130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086500-A-G

38651348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086267-T-C

38651579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086028-A-G

38651969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085516-G-A

38652154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085353-C-T

http://identifiers.org/hco/5/GRCh38#38652368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7082873-A-C

38652457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082783-G-A

http://identifiers.org/hco/5/GRCh38#38653116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7082104-C-A

38653129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: non coding transcript exon variant
orthologous variants: 7082096-T-C

38653192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082056-T-C

38653211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082037-G-C

38653211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082037-G-T

http://identifiers.org/hco/5/GRCh38#38653217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7082031-C-A

38653217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082031-C-T

38653263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081984-C-T

38653274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081973-G-A

38653274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081973-G-T

38653380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081853-C-T

38653755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081476-C-T

http://identifiers.org/hco/5/GRCh38#38653867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7081365-C-A

http://identifiers.org/hco/5/GRCh38#38654008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7081220-C-A

38654008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081220-C-T

38654043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081184-G-A

38654627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080981-C-T

38654658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080953-G-T

38655839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079974-C-G

38655874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079936-G-A

38655918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079884-G-A

38655918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079884-G-T

38656242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078969-T-A

38656330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078890-A-T

38657063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078336-C-T

38657221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078178-T-C

38657286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078109-A-G

38657289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078106-T-C

38657302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078095-A-G

38657306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078091-G-T

38657308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078089-G-A

38657452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7077988-T-A

38658062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076986-G-A

38661144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075150-G-T

38661147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075145-A-G

http://identifiers.org/hco/5/GRCh38#38661356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7074978-C-A

38662010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074227-A-T

38662181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074048-T-G

38662215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074014-C-T

38662531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7073686-G-A

38663182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7072338-G-T

38663553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7071620-A-G

http://identifiers.org/hco/5/GRCh38#38664602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7071043-C-A

38664617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7071028-C-T

38664638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070991-T-A

38664678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070950-A-T

38664785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070862-G-A

38664822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070825-A-G

38664895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070759-G-A

38665057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070505-G-A

38665085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070465-T-G

38665142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070292-A-G

38665237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070196-T-G

38665376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070105-A-G

38665502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070016-T-C

38665591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069919-G-A

38665638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069870-T-A

38665661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069846-G-A

38665691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069818-C-T

38665822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069695-C-T

38666234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069609-T-G

38666453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069405-G-C

38666537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069351-G-T

38666659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069235-G-A

38666659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069235-G-C

38666809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069114-G-T

38667248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068673-C-T

38667441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068528-G-A

38667470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068500-G-C

38667590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068184-T-C

38667883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067882-C-T

38668086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067684-G-T

38668446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067354-G-A

38668841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066961-T-A

38668864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066947-A-G

38668884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066927-A-G

38669344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066622-A-G

38669360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066606-G-A

38669360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066606-G-T

38669454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066512-T-C

38669460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066506-T-C

38669476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066505-C-G

38669623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066366-T-C

38669969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066135-C-T

38670029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066071-A-G

38670053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066060-T-A

38670053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066060-T-C

38670170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065942-G-A

38670171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065941-G-C

38670178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065934-G-T

38670197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065914-G-A

38670394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065711-G-A

38670394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065711-G-T

38670465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065648-C-T

38670749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065354-T-G

38670979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065111-G-T