119593778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116221238-G-A

http://identifiers.org/hco/12/GRCh38#119593801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116221215-A-C

119593801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116221215-A-G

119593837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116221179-C-T

119593984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116221029-T-C

119593984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116221029-T-G

119594117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220932-T-A

119594251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220870-G-A

119594251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220870-G-T

119594295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220829-G-A

119594295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220829-G-T

119594310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220818-T-C

119594332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220805-T-C

119594338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220802-G-A

119594348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220792-C-T

119594383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220761-G-A

119594383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220761-G-T

119594453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220712-G-A

119594453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220712-G-T

119594460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220705-G-T

119594556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220610-C-T

http://identifiers.org/hco/12/GRCh38#119594574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116220593-C-A

119594574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220593-C-T

119594634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220541-G-A

119594634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220541-G-T

119594722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220447-C-G

119594737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220432-G-A

119594737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220432-G-C

119594737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220432-G-T

119594739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116220430-C-T

119594910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116220279-G-A

119595093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220184-C-T

119595208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220109-G-C

119595208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116220109-G-T

119595424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116219924-T-C

119595647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219727-T-C

119595782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219584-G-A

119595782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219584-G-T

119595899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219326-G-T

119595961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219259-C-T

119596101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219099-C-T

119596164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116219032-A-G

119596457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116218727-G-A

119596460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116218724-G-C

119596460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116218724-G-T

119597215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116217475-A-T

119597392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116216745-A-G

119597530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116216624-C-T

119598196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215554-A-G

119598203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116215493-C-T

http://identifiers.org/hco/12/GRCh38#119598834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116215042-C-A

119599148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116214636-G-A

119600277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212549-A-G

119600322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212506-A-G

119600408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212408-A-G

http://identifiers.org/hco/12/GRCh38#119600413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116212403-C-A

119600413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212403-C-T

119600515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116212201-A-G

119600931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116211835-A-G

http://identifiers.org/hco/12/GRCh38#119600964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116211805-C-A

119601132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116211635-A-G

119601185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116211582-C-G

119601327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116211446-T-C

119601359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116211414-G-T

119602205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116210487-C-T

119602916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116209604-T-G

119603431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116209444-A-G

119603588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116209280-C-G

119605749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208685-A-G

119605975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208469-G-A

119605975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208469-G-T

119605992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208457-G-C

119606297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208139-A-G

119606302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116208134-G-A

119606419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116207990-G-C

119614478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197515-G-A

119614479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197514-C-T

119614673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116197337-C-G

119615534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196589-G-T

119615605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196519-T-C

119615651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196474-T-C

119615880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196259-G-A

119616040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116196097-G-T

119616264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195877-A-G

119616493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116195656-G-T

119621704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194775-A-T

119621705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116194774-C-G

119621805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193836-G-T

119622211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193164-T-C

http://identifiers.org/hco/12/GRCh38#119622258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116193122-C-A

119622264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116193116-G-A

119622428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116192864-G-C

119623327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191392-A-G

119623330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191389-G-T

119623342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191366-G-C

119623346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191362-G-A

119623348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191360-T-G

119623352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191352-G-A

http://identifiers.org/hco/12/GRCh38#119623420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116191284-C-A

119623420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116191284-C-T

119628931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116190356-G-A

119629231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116190002-A-G

119629266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189965-C-T

119629270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189960-C-T

119629280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189950-G-C

119629341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189899-C-G

http://identifiers.org/hco/12/GRCh38#119629702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116189545-C-A

119629702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189545-C-G

119629711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189536-C-T

http://identifiers.org/hco/12/GRCh38#119629730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116189517-C-A

119629784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189463-G-A

119629784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189463-G-C

http://identifiers.org/hco/12/GRCh38#119629787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116189460-C-A

119629787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189460-C-T

119629811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189436-G-A

119629811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189436-G-C

119629823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189424-A-G

119629823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189424-A-T

http://identifiers.org/hco/12/GRCh38#119629838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116189409-A-C

119629838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189409-A-G

119629841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189406-G-A

119629841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116189406-G-T

119629879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116189368-A-T

119629880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116189367-G-T

http://identifiers.org/hco/12/GRCh38#119629918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116189327-C-A

119629918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189327-C-T

119629930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189310-G-A

119629930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189310-G-T

119629987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116189208-T-C

119630420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188722-A-T

119630687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188467-T-C

119630704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188452-C-T

119630742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188409-C-T

119630940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188204-G-A

119630940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188204-G-T

http://identifiers.org/hco/12/GRCh38#119630953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116188191-C-A

119630953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188191-C-T

119630963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188187-G-C

http://identifiers.org/hco/12/GRCh38#119631007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116188141-C-A

119631007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188141-C-T

119631052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188096-A-T

119631082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116188077-G-A

119631105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116188054-A-G

119631200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187999-T-C

http://identifiers.org/hco/12/GRCh38#119631212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187987-C-A

119631212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187987-C-T

119631216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187983-A-G

http://identifiers.org/hco/12/GRCh38#119631217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187982-C-A

http://identifiers.org/hco/12/GRCh38#119631341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187888-C-A

119631341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187888-C-G

http://identifiers.org/hco/12/GRCh38#119631369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187862-C-A

119631369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187862-C-T

119631370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187861-A-G

119631370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187861-A-T

http://identifiers.org/hco/12/GRCh38#119631385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187846-C-A

119631385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116187846-C-G

119631389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116187842-T-A

119631427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116187804-G-T

119631476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116187752-G-A

119631547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116187687-T-C

http://identifiers.org/hco/12/GRCh38#119631596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116187613-C-A

119631596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116187613-C-T

119631597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116187612-G-A

119631603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 116187606-G-T

119631636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116187573-G-A

119631636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116187573-G-T

119631687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186983-C-G

http://identifiers.org/hco/12/GRCh38#119631688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116186982-A-C

119631729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186940-A-G

119631755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186933-A-G

119631783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186905-T-C

119631787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186901-C-G

119631787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186901-C-T

119631853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186874-C-T

119632257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186486-G-A

119632396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116185828-G-A

119632530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116185712-G-C

119632576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116185676-C-T

119632733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116185544-T-A

119632805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116185177-A-G

119632872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116185109-T-A

http://identifiers.org/hco/12/GRCh38#119633213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116184392-A-C

119633259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184347-T-C

119633269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184337-T-C

119633348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184303-G-A

119633484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184244-G-A

119633571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184219-A-G

119633651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184171-G-A

119633651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116184171-G-C

119634045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183867-A-G

http://identifiers.org/hco/12/GRCh38#119634116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116183800-C-A

119634116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183800-C-T

119634117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183799-T-C

119634117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183799-T-G

http://identifiers.org/hco/12/GRCh38#119634121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116183795-C-A

119634176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183739-G-A

119634227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116183676-G-A

119634300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183605-G-A

119634300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183605-G-C

119634300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183605-G-T

119634315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183593-A-G

119634315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116183593-A-T

119634796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116182338-A-G

119634940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116182209-A-G

119635062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116182096-C-T

119635127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116182047-A-G

119635160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116182013-C-G

119635266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116181909-G-A

119636884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116180206-G-A

119637026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116180077-C-G

119637151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116179950-G-T

119637745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116179663-G-A

119637762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116179646-T-C

119640637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116178898-A-G

119640674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116178861-C-G

119640674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116178861-C-T

http://identifiers.org/hco/12/GRCh38#119640697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116178830-A-C

119640802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116178727-G-A

119640802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116178727-G-T

http://identifiers.org/hco/12/GRCh38#119640817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116178712-C-A

119640875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178666-T-A

119640875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178666-T-C

119640875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178666-T-G

http://identifiers.org/hco/12/GRCh38#119640892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116178649-C-A

119640923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178616-T-C

119641037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178515-C-T

119641082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178474-G-A

119641082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178474-G-T

119641090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178466-A-G

119641103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178453-G-T

119641408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178217-A-T

119641581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178065-G-A

119641581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116178065-G-T

119641643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177986-A-G

119641749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177881-A-G

119641778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177844-G-C

http://identifiers.org/hco/12/GRCh38#119641866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116177758-C-A

119641866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177758-C-T

119641881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177744-T-C

119641961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177660-G-T

119642138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177508-G-A

119642138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177508-G-T

http://identifiers.org/hco/12/GRCh38#119642162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116177480-C-A

119642162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177480-C-T

119642175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177464-C-T

119642177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177462-G-A

119642241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177399-G-T

119642588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116177272-T-C

119642914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116176959-A-G

119643041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116176842-G-T

http://identifiers.org/hco/12/GRCh38#119643068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116176815-C-A

119643090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176759-T-C

119643093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176756-T-G

119643109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176732-C-G

119643146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176694-A-T

119643364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176486-G-A

119643407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176435-A-T

119643415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176427-G-A

119643444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116176404-C-G