160188188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43517554-T-C

160188609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, undefined
orthologous variants: 43517235-C-T

160189411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43516121-T-C

160189499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43516043-T-C

160189533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43516010-G-A

160189537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43516006-C-G

160189541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43516002-C-G

160189837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43515814-G-T

160189863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43515788-A-G

160192326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43512140-C-G

160192347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43512119-C-T

160192452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43512056-G-A

160192456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43512052-A-G

160192533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511970-C-T

160192599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511912-G-C

160192659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511843-C-G

160192659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511843-C-T

160192729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511789-G-C

http://identifiers.org/hco/5/GRCh38#160192736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43511782-C-A

160192736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511782-C-T

160192761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43511757-G-A

160196370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510417-C-G

http://identifiers.org/hco/5/GRCh38#160196392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43510396-C-A

160196502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510178-T-C

160196532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510147-G-A

160196532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510147-G-C

160196532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510147-G-T

160197342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43509323-A-G

http://identifiers.org/hco/5/GRCh38#160197405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43509265-C-A

http://identifiers.org/hco/5/GRCh38#160197406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43509264-C-A

160197410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43509260-T-C

160197444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43509222-T-A

160197460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43509206-A-G

160197594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43509057-G-T

160197614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43509044-A-G

http://identifiers.org/hco/5/GRCh38#160197652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43509000-C-A

160197744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508910-G-T

http://identifiers.org/hco/5/GRCh38#160197880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43508826-C-A

160197880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43508826-C-T

160197979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43508776-T-A

160197979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43508776-T-G

160198048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43508708-G-A

160198048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43508708-G-T

160198097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508662-G-T

160198120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508655-G-T

http://identifiers.org/hco/5/GRCh38#160198122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43508653-C-A

160198122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508653-C-T

160198262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508529-G-A

160198262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508529-G-T

http://identifiers.org/hco/5/GRCh38#160198316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43508484-C-A

160198316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43508484-C-T

160198978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43504498-A-G

160198978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43504498-A-T

160199085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43504395-G-C

160199112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43504370-G-A

160199202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504320-G-C

http://identifiers.org/hco/5/GRCh38#160199208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43504314-C-A

160199208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43504314-C-T

http://identifiers.org/hco/5/GRCh38#160199209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43504313-C-A

160199209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43504313-C-T

160199241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43504295-G-C

160199489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43504146-G-A

160199489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43504146-G-C

160199571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43504068-C-T

160199689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43503974-G-T

160199828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43503850-C-T

160199866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503812-G-A

160200128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503598-A-G

160200223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43503538-T-C

160201089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43502688-C-T

160204683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501769-G-A

160204712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501740-A-G

160204730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43501734-A-G

160204774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43501689-A-G

160204774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43501689-A-T

160204810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43501654-G-A

160204810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43501654-G-T

160204828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43501636-G-A

160204828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43501636-G-T

160204832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501632-G-A

160204832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501632-G-T

160204906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501574-T-C

160204944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501532-T-G

160204952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501524-T-A

160204952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501524-T-C

http://identifiers.org/hco/5/GRCh38#160204953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43501523-A-C

160204953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501523-A-G

160204958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501518-T-C

160204958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501518-T-G

160205110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43501425-A-G

160209831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43500342-A-G

160210323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499909-T-C

160210431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499801-A-G

160210481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499746-G-A

http://identifiers.org/hco/5/GRCh38#160210934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43499383-C-A

160210944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499373-T-C

160210960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499356-C-T

http://identifiers.org/hco/5/GRCh38#160210963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43499353-C-A

160210963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499353-C-T

http://identifiers.org/hco/5/GRCh38#160210993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43499323-A-C

160211070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43499235-C-T

160211141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: intron variant
orthologous variants: 43498548-C-T

160215168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43497794-T-C

160215333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43497634-G-A

160215357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43497610-T-C

160215409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43497559-A-T

160215692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43497207-A-G

http://identifiers.org/hco/5/GRCh38#160219183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43495543-A-C

160219259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495469-C-T

160219309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495419-G-A

160219435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495310-G-A

160219584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495202-A-G

160219596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495190-T-A

160219651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43495153-G-A

http://identifiers.org/hco/5/GRCh38#160219756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43495065-C-A

160229045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492780-A-T

160229103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492729-G-A

160229103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492729-G-T

160229112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492721-G-A

160229173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492681-C-T

160229204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492662-G-C

160229267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492621-A-T

160229284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492603-A-G

160229284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492603-A-T

http://identifiers.org/hco/5/GRCh38#160229298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43492592-C-A

http://identifiers.org/hco/5/GRCh38#160229386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43492503-C-A

160229386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492503-C-T

160229400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492489-G-T

160229490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492402-T-A

160229490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492402-T-C

160229516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43492376-C-G

160229516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43492376-C-T

160229519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43492373-C-G

160229519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43492373-C-T

http://identifiers.org/hco/5/GRCh38#160229531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43492365-C-A

160229540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 43492357-C-T

http://identifiers.org/hco/5/GRCh38#160229717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43492131-A-C

160229717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492131-A-T

http://identifiers.org/hco/5/GRCh38#160229720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43492128-C-A

160229720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492128-C-T

160229721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492127-A-G

160229742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492106-T-C

160229746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492102-T-G

160229752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492096-C-T

160229819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43492020-C-G

160230251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491967-G-A

160230433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491804-T-C

160230447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491790-G-A

160230610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491665-C-G

160230719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491539-G-A

160230795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491463-A-G

160230903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491359-T-C

160231010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43491200-A-G

160231725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43490519-C-T

http://identifiers.org/hco/5/GRCh38#160231824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489827-C-A

160231843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43489814-A-G

http://identifiers.org/hco/5/GRCh38#160231935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489731-C-A

160231935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43489731-C-T

http://identifiers.org/hco/5/GRCh38#160231940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489704-C-A

160231940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43489704-C-T

160231959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43489683-G-A

160231959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43489683-G-T

http://identifiers.org/hco/5/GRCh38#160231960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489682-C-A

160231960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43489682-C-T

http://identifiers.org/hco/5/GRCh38#160231974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489669-C-A

160231974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43489669-C-T

160231976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43489667-T-C

http://identifiers.org/hco/5/GRCh38#160232033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489635-C-A

160232033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43489635-C-T

160232109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43489559-G-A

http://identifiers.org/hco/5/GRCh38#160232296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489372-C-A

160232296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43489372-C-T

160232355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43489311-A-G

http://identifiers.org/hco/5/GRCh38#160232388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489296-C-A

160232388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43489296-C-T

http://identifiers.org/hco/5/GRCh38#160232397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489290-C-A

http://identifiers.org/hco/5/GRCh38#160232424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43489264-C-A

160232424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43489264-C-T

160232461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43489218-A-G

160237101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487509-T-C

160237101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487509-T-G

160237107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487503-G-C

160237159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487449-C-G

160237209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487401-C-T

http://identifiers.org/hco/5/GRCh38#160237213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43487395-A-C

160238303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487309-G-T

160238375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487231-G-T

160238389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487217-C-T

http://identifiers.org/hco/5/GRCh38#160238403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43487205-C-A

160238403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487205-C-G

160238403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487205-C-T

160238474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487134-G-A

160238474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487134-G-T

160238507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487102-A-G

160238507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487102-A-T

http://identifiers.org/hco/5/GRCh38#160238508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43487101-C-A

160238508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487101-C-T

160238519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487090-G-A

160238525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487084-A-G

160238525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487084-A-T

http://identifiers.org/hco/5/GRCh38#160238528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43487081-C-A

160238528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487081-C-G

160238528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487081-C-T

160238542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487067-G-A

160238542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487067-G-T

http://identifiers.org/hco/5/GRCh38#160238543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43487066-C-A

160238543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487066-C-T

160238545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487064-G-A

160238545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487064-G-T

160238568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487028-G-A

160238568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43487028-G-T

160238606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 43486990-G-A

160238606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 43486990-G-T

160238633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43486963-G-A

160238633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43486963-G-C

http://identifiers.org/hco/5/GRCh38#160238669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43486927-C-A

http://identifiers.org/hco/5/GRCh38#160238724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43486872-C-A

160238724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3561
most severe consequence: 3 prime UTR variant
orthologous variants: 43486872-C-T