153792647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286346-C-G

153792647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286346-C-T

153792682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286313-G-A

153792682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286313-G-T

153792840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286190-G-T

153793040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90286022-G-A

153793541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90285593-G-A

153793687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90285439-G-A

http://identifiers.org/hco/1/GRCh38#153793830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90285299-C-A

153793841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90285283-G-A

153793859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90285258-A-G

153793928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90285203-C-T

153793958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285173-A-G

153793975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285155-G-A

153793975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285155-G-T

153794082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285044-G-A

153794082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285044-G-C

153794082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285044-G-T

153794097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90285030-G-A

http://identifiers.org/hco/1/GRCh38#153794129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90284998-C-A

153794129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90284998-C-T

153794146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90284980-G-A

153794146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90284980-G-T

http://identifiers.org/hco/1/GRCh38#153794190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90284937-C-A

153794190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90284937-C-T

153794238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284873-A-G

153794238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284873-A-T

153794243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284868-G-T

153794261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284850-G-A

153794284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284825-G-A

153794284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284825-G-T

153794288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284821-G-A

153794296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284815-G-A

153794303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284808-G-A

153794303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284808-G-T

153794314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284795-A-T

153794485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284439-G-A

http://identifiers.org/hco/1/GRCh38#153794499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90284425-C-A

153794499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284425-C-T

153794676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90284197-G-T

153794826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90283961-G-A

153794826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90283961-G-T

153794965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90283851-C-T

http://identifiers.org/hco/1/GRCh38#153795098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283717-C-A

153795098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90283717-C-G

http://identifiers.org/hco/1/GRCh38#153795139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283676-C-A

153795139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90283676-C-T

http://identifiers.org/hco/1/GRCh38#153795182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283638-C-A

153795182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283638-C-T

http://identifiers.org/hco/1/GRCh38#153795204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283612-C-A

153795204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283612-C-T

153795320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283508-T-C

153795408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283434-G-A

153795408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283434-G-T

153795541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283298-G-A

153795541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283298-G-T

153795553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283286-G-A

153795553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283286-G-T

153795569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283270-T-C

http://identifiers.org/hco/1/GRCh38#153795650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283214-C-A

153795650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283214-C-T

http://identifiers.org/hco/1/GRCh38#153795680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283182-C-A

153795680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283182-C-T

http://identifiers.org/hco/1/GRCh38#153795687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90283175-C-A

153795687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90283175-C-T

153795772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283109-C-T

153795783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283099-G-T

153795822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90283060-G-T

153796060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281916-C-G

153796060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281916-C-T

http://identifiers.org/hco/1/GRCh38#153796061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90281915-C-A

153796080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281896-G-T

http://identifiers.org/hco/1/GRCh38#153796081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90281895-C-A

153796081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281895-C-T

153796192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281820-C-T

http://identifiers.org/hco/1/GRCh38#153796194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90281818-C-A

153796194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281818-C-T

http://identifiers.org/hco/1/GRCh38#153796291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90281723-C-A

153796291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90281723-C-T

153796297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90281717-C-T

153796315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90281700-C-T

153796411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281607-G-A

153796411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281607-G-T

153796432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90281586-G-A

http://identifiers.org/hco/1/GRCh38#153796499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90281531-C-A

153796499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90281531-C-T

153796526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90281504-T-C

153796710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281369-T-C

153796769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281317-T-C

153796855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281244-C-T

153797047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281133-G-A

153797047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90281133-G-C

153797499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90280805-A-G

153797501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90280803-A-T

153797505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90280799-A-G

153797505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90280799-A-T

153797506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90280798-T-C

153797789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279609-G-A

http://identifiers.org/hco/1/GRCh38#153797805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90279595-A-C

153797852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279548-T-C

153797852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279548-T-G

153797885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279515-G-A

http://identifiers.org/hco/1/GRCh38#153797900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90279504-C-A

153797900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279504-C-G

153797900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279504-C-T

153797921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279482-G-A

http://identifiers.org/hco/1/GRCh38#153798039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90279322-C-A

153798039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279322-C-T

153798213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90279140-T-A

153798446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90278974-G-A

153798511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90278918-G-A

153798703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90278773-T-G

153799138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90276775-T-G

153799213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90276718-G-C

153799286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90276582-A-G

153799712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90276212-G-A

153799712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90276212-G-T

153799727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90276196-G-A

153799728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90276195-T-C

http://identifiers.org/hco/1/GRCh38#153799826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90275368-C-A

153799826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275368-C-T

http://identifiers.org/hco/1/GRCh38#153799851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90275343-C-A

153799851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275343-C-T

153800086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275140-C-T

http://identifiers.org/hco/1/GRCh38#153800096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90275130-C-A

153800096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275130-C-T

153800119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275107-G-A

153800119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275107-G-T

153800139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90275087-A-G

153800267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274811-T-A

153800267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274811-T-C

http://identifiers.org/hco/1/GRCh38#153800276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90274802-C-A

153800330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274762-T-A

153800330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274762-T-C

153800368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274724-T-A

153800369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274723-G-A

http://identifiers.org/hco/1/GRCh38#153800379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90274713-C-A

153800379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274713-C-G

153800379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274713-C-T

153800476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 90274618-T-C

153800531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90274567-G-T

http://identifiers.org/hco/1/GRCh38#153800625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90274470-C-A

153800805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274320-G-T

153800856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274278-G-T

153801070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274101-C-T

153801107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274062-G-T

153801113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274056-G-A

153801113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90274056-G-T

153801182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90274000-G-A

153801182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90274000-G-C

153801184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273998-C-T

153801185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273997-C-G

153801185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273997-C-T

153801195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273987-G-A

153801195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273987-G-T

153801206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273976-G-T

153801272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273915-G-A

153801272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273915-G-T

153801284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273904-G-A

153801284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273904-G-T

153801401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90273795-T-C

153801640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90273677-A-G

http://identifiers.org/hco/1/GRCh38#153801778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90273548-C-A

153801778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273548-C-T

153801825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 90273513-G-A

153801825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 90273513-G-T

http://identifiers.org/hco/1/GRCh38#153801901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90273430-C-A

153801918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90273363-G-A

153801918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90273363-G-T

http://identifiers.org/hco/1/GRCh38#153802060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90273251-A-C

153802060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90273251-A-G

153802499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90272932-G-A

153803881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90271573-C-T

153804264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90271199-A-G

153804995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90270415-T-A

153804995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90270415-T-C

http://identifiers.org/hco/1/GRCh38#153805015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90270395-C-A

153805015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90270395-C-G

153805015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90270395-C-T

http://identifiers.org/hco/1/GRCh38#153805018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90270393-C-A

153805194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90270200-T-A

153805194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90270200-T-G

153805383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90270028-G-T

153805501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269920-T-A

153805501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269920-T-C

http://identifiers.org/hco/1/GRCh38#153805503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90269918-C-A

153805503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269918-C-T

153805547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90269882-T-C

153805633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269800-C-T

153805869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269594-G-T

http://identifiers.org/hco/1/GRCh38#153805891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90269573-C-A

153806062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269428-G-T

153806388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269102-G-T

153806416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269073-G-A

http://identifiers.org/hco/1/GRCh38#153806451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90269038-C-A

153806451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269038-C-T

153806475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269014-T-A

153806475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90269014-T-C

153806624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268860-T-C

http://identifiers.org/hco/1/GRCh38#153806751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90268734-A-C

153806751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268734-A-G

153806770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268718-G-A

153806817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268695-G-A

153806943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268570-T-C

153807029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90268485-T-C

http://identifiers.org/hco/1/GRCh38#153807111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90268403-C-A

http://identifiers.org/hco/1/GRCh38#153807144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90268370-C-A

153807633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267844-G-A

153807745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267734-G-A

153807745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267734-G-T

153807797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267691-T-A

153807797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267691-T-C

153807797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267691-T-G

153808300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267188-A-G

153808413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267074-C-G

153808413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90267074-C-T

http://identifiers.org/hco/1/GRCh38#153808480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90266974-A-C

153808480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90266974-A-G

http://identifiers.org/hco/1/GRCh38#153808582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90266877-C-A

153808925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90266532-C-T

153809754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265727-A-T

153809870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265616-T-C

http://identifiers.org/hco/1/GRCh38#153809919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90265568-C-A

153809919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265568-C-T

153809966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265521-G-A

153809966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265521-G-T

http://identifiers.org/hco/1/GRCh38#153810068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90265413-C-A

153810068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90265413-C-T

153811236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90265010-A-G

153812006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90263134-G-A

153812006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90263134-G-T

153812720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90262527-G-A

http://identifiers.org/hco/1/GRCh38#153816625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90259085-C-A

153816625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90259085-C-T

http://identifiers.org/hco/1/GRCh38#153816637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90259078-C-A

153816637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90259078-C-G

153816672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90259046-A-G

http://identifiers.org/hco/1/GRCh38#153817256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90258980-C-A

153817436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: missense variant
orthologous variants: 90258815-G-A

153817436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: missense variant
orthologous variants: 90258815-G-C

153817436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: missense variant
orthologous variants: 90258815-G-T

153817588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90258675-G-A

153817588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90258675-G-T

153817595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90258668-A-G

153817630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90258634-A-G

153817638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90258624-T-C

http://identifiers.org/hco/1/GRCh38#153817999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90257864-C-A

153817999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90257864-C-T

153818347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90257410-C-T

153818385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90257368-G-A

153818734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256827-C-T

http://identifiers.org/hco/1/GRCh38#153818738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90256823-C-A

153818738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256823-C-T

153818781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256802-G-A

153819057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256526-G-A

153819057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256526-G-C

153819057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256526-G-T

153819581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256092-G-A

153819581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256092-G-T

http://identifiers.org/hco/1/GRCh38#153819583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90256090-A-C

153819585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90256088-G-T

153825787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90250740-T-C

153825896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90250652-T-C

153827378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90250470-T-C

153827549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90250187-G-T

153827595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90250144-T-C

http://identifiers.org/hco/1/GRCh38#153827939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90249375-C-A

153827939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90249375-C-T

http://identifiers.org/hco/1/GRCh38#153827966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90249348-C-A

153827966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90249348-C-T

153827996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90249316-G-A

153828093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90249216-A-G

153828148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, missense_variant
orthologous variants: 90249161-T-A

153828148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, missense_variant
orthologous variants: 90249161-T-C

153828358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90248951-G-A

153828358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90248951-G-C

153828430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90248892-T-C

153881017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90230805-T-G

153881364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90230421-A-G

153881593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90230216-A-T

153881597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90230212-G-C

153881949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90229890-G-A

http://identifiers.org/hco/1/GRCh38#153881968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90229869-A-C

153882003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90229836-G-A

153882185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90229646-T-G

153882190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90229641-A-G

153883156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90228391-T-C

153888537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90226231-T-C

153891947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223566-A-G

153892147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223280-G-A

153892147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223280-G-C

153892147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223280-G-T

http://identifiers.org/hco/1/GRCh38#153892188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90223238-A-C

http://identifiers.org/hco/1/GRCh38#153892198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90223228-C-A

153892198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223228-C-T

153892210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90223221-G-A

http://identifiers.org/hco/1/GRCh38#153892217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90223202-C-A

http://identifiers.org/hco/1/GRCh38#153892230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90223180-A-C

153915999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90210940-G-T

153916032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90209600-T-G

153916253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90209441-T-A

153916253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90209441-T-G

153916518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90209212-A-G

153918726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90205981-G-C

153918953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90205781-A-G

153919653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90204910-T-C

153920840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90202719-C-G

http://identifiers.org/hco/1/GRCh38#153920865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90202699-A-C

153921377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90202039-T-C

http://identifiers.org/hco/1/GRCh38#153921556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90201884-A-C

http://identifiers.org/hco/1/GRCh38#153921775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90201717-C-A

153921776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90201715-T-C

http://identifiers.org/hco/1/GRCh38#153921862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90201626-C-A

153921862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90201626-C-T

http://identifiers.org/hco/1/GRCh38#153922231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90201225-A-C

153922236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90201218-G-A

http://identifiers.org/hco/1/GRCh38#153922510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90200955-C-A

153922594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90200874-T-G

153922605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90200863-C-T

http://identifiers.org/hco/1/GRCh38#153922687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90200791-C-A

153922687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90200791-C-T

153922852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90200609-G-T

153923072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, undefined
orthologous variants: 90200387-G-A

http://identifiers.org/hco/1/GRCh38#153923074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#90200385-C-A

153923074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, undefined
orthologous variants: 90200385-C-T

153923096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron variant
orthologous variants: 90200363-C-T

153923150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, undefined
orthologous variants: 90200309-G-A

153923150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30778
most severe consequence: intron_variant, undefined
orthologous variants: 90200309-G-T