14470731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42883403-A-G

14470909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42883584-A-T

14470924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42883599-T-C

14470928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42883603-A-G

http://identifiers.org/hco/4/GRCh38#14470966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42883641-C-A

14470966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42883641-C-T

14476408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42883759-G-C

14476408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42883759-G-T

14476425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42883771-G-A

14476430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42883776-G-T

14476538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42883897-T-A

14476753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884094-T-C

14476753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884094-T-G

14476877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884206-G-A

14477133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884462-G-C

14477201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884530-A-G

http://identifiers.org/hco/4/GRCh38#14477225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42884554-C-A

14477257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884582-G-A

14477257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884582-G-T

14477357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42884678-G-A

14477357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42884678-G-C

14477357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: non coding transcript exon variant
orthologous variants: 42884678-G-T

14477429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42884750-A-G

14477479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884808-G-A

14477479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884808-G-T

14477504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884833-A-G

http://identifiers.org/hco/4/GRCh38#14477574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42884895-C-A

14496631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885597-A-G

14496690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885538-A-G

14496884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885349-A-T

14496885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885348-A-T

14496886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885347-T-A

14497229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42885007-T-C

14497251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42884985-T-C

14508215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887194-C-T

14508335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887276-A-G

14508388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887324-G-A

14508388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887324-G-T

14508668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887522-C-G

http://identifiers.org/hco/4/GRCh38#14508671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42887525-C-A

14508671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887525-C-G

14508736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887586-G-T

14508758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887603-A-G

14508779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887619-C-T

14508867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887702-A-G

14508875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42887710-G-A

http://identifiers.org/hco/4/GRCh38#14509267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42896301-A-C

14509267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896301-A-G

14509268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896302-C-G

14509353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896384-C-T

http://identifiers.org/hco/4/GRCh38#14509499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42896521-A-C

14509538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896540-G-A

14510033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896864-C-G

14510163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896973-T-C

http://identifiers.org/hco/4/GRCh38#14510526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42897323-A-C

http://identifiers.org/hco/4/GRCh38#14510533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42897330-A-C

14510672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42897447-T-C

14510711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42897483-G-C

14510831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42897579-T-C

http://identifiers.org/hco/4/GRCh38#14511130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42897707-C-A

14511979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42898377-G-A

14512053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42898481-A-G

14512082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42898510-G-A

14512118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42898546-T-C

14512150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42898605-G-A

14514087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42899939-T-C

14514242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42900090-C-T

14517621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42915267-C-G

14518167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42915820-T-C

14518318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42915964-G-A

14518422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42916089-G-A

14518432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42916099-T-C

14518543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916211-C-T

14518545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916213-A-G

14518622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916283-C-T

14518728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916391-G-A

14518995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916633-T-C

14519073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916711-G-A

14519200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916833-C-T

14519203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916836-G-A

14519213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916845-G-A

http://identifiers.org/hco/4/GRCh38#14519339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42916967-A-C

14519339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916967-A-T

14519359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916987-G-C

14519366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916994-C-G

14519366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916994-C-T

14519634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917256-G-T

14520113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917759-G-C

14520338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918716-T-C

14520666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919037-A-G

14521019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919391-A-T

14521020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919392-T-A

14521132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919521-T-C

http://identifiers.org/hco/4/GRCh38#14521189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42919586-A-C

14521189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919586-A-G

14521274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919668-T-G

14521392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919782-A-G

14521473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919862-G-A

14521476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42919865-G-T

14521623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920008-G-C

14521911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920326-A-G

14521919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920346-T-C

14522073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920570-C-G

14522210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920676-C-T

14522467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920852-T-C

14522513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920871-G-C

http://identifiers.org/hco/4/GRCh38#14522551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42920909-C-A

14522683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921036-G-A

14522916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921273-A-G

14523148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921497-A-T

14523206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921559-G-C

14523252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921605-G-A

14523449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921827-C-T

14523522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921913-A-G

14523522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921913-A-T

14523533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921939-G-C

14523768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922212-A-G

14523777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922221-A-G

14523824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922265-C-T

14523877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922332-T-A

http://identifiers.org/hco/4/GRCh38#14524181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42922625-A-C

http://identifiers.org/hco/4/GRCh38#14524214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42922652-C-A

14536790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925983-G-A

14536862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42926069-C-T

14536959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42926160-C-T

14537110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42926311-C-T

14537296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42926500-C-G

14537612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42927080-T-C

14547069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42930838-G-A

14547085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42930862-A-G

14547344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931115-C-T

14547592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931349-C-T

14547665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931422-G-T

14547666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931423-C-T

http://identifiers.org/hco/4/GRCh38#14550615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42933017-A-C

14550637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933039-G-A

http://identifiers.org/hco/4/GRCh38#14550658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42933060-A-C

14550658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933060-A-G

14550820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933838-G-A

14550826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933844-G-T

14550843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933861-G-C

14550885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933904-G-T

14551070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934083-G-A

http://identifiers.org/hco/4/GRCh38#14551071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42934084-A-C

14551071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934084-A-G

14551351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934299-A-G

14551570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934494-G-A

14551649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934564-C-T

14551777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934693-T-C

14552448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935324-G-A

14552464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935340-G-C

14556755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937497-G-A

14556814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937552-G-A

14556900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937646-T-G

14556980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937726-T-G

http://identifiers.org/hco/4/GRCh38#14557025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42937773-A-C

14557183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937920-G-A

14557215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937943-G-T

14557323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938054-G-C

14557551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938374-G-A

14557710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938532-G-A

14557760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938581-A-G

14557766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938587-G-T

14557921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938748-T-C

http://identifiers.org/hco/4/GRCh38#14557972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42938819-C-A

14558086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938932-G-T

http://identifiers.org/hco/4/GRCh38#14558108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42938951-C-A

14558248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939091-G-T

14558692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939644-T-C

14558943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939810-A-G

14558964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939831-A-G

14558998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939866-G-C

14559324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42940173-A-G

14559470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42940317-T-C

14559652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42940771-G-A

14559785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42940905-T-C

http://identifiers.org/hco/4/GRCh38#14559858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42940978-A-C

14560026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42941125-T-G

http://identifiers.org/hco/4/GRCh38#14560171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42941260-C-A

14560406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42941474-C-T

14560496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42941560-T-C

14560594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42941657-A-G

14564400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943302-G-C

14564630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943507-T-C

14564994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943766-G-A

14565054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943815-T-C

14565080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943842-A-G

14565094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943856-G-T

14565106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943866-C-G

14565142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943912-G-A

14565158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943928-G-C

14565213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42943982-T-C

14565431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42944209-G-A

14565431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42944209-G-T

14566613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945031-G-C

14566661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945073-G-A

http://identifiers.org/hco/4/GRCh38#14566800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42945210-C-A

14567030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945652-C-T

14567106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945714-T-C

14567107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945715-A-G

14567159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945767-G-A

14567174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945782-C-T

14567175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945783-T-G

14567319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945933-T-C

14567319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945933-T-G

14567392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945991-G-T

14567398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42945997-T-A

http://identifiers.org/hco/4/GRCh38#14567458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42946057-C-A

14567497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42946097-T-G

14567893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42946828-C-T

http://identifiers.org/hco/4/GRCh38#14567943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42946871-C-A

14567948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42946876-G-T

14568509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42950517-C-T

14570275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953202-T-C

14570285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953211-C-T

14570334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953260-C-T

14570448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953374-T-A

14570455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953381-C-T

http://identifiers.org/hco/4/GRCh38#14570562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42953488-C-A

14570562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953488-C-T

14570683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42953608-G-A

14571790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42954119-G-C

14572060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42954407-T-C

14572065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42954412-C-G

14572320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42955466-A-G

14572478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42955755-C-T

14572533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42955808-G-C

14572608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42955883-G-A

14572706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42955981-G-T

http://identifiers.org/hco/4/GRCh38#14572831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42956086-C-A

14572841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42956096-C-T

14572895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42956147-A-G

14572904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42956156-G-A

14572904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42956156-G-C

14573645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957352-A-T

http://identifiers.org/hco/4/GRCh38#14573782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42957446-C-A

14573843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957508-A-G

14573843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957508-A-T

14573905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957576-C-T

14574014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957682-G-A

14574014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957682-G-C

14574184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957841-T-C

14574247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42957896-C-T

14574736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958378-G-A

14574779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958421-G-T

14575309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958630-C-T

14575360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958681-A-G

14575400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958700-T-C

14575521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958799-C-T

14575555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958833-G-A

14575560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42958840-T-G

14575749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959018-A-G

14575760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959030-G-A

14575804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959073-G-A

14575854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959111-T-C

14581505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959919-G-T

14581586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959984-C-T

14581598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42959996-A-G

http://identifiers.org/hco/4/GRCh38#14581665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42960062-C-A

http://identifiers.org/hco/4/GRCh38#14581688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42960071-C-A

14581848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960197-C-T

14581880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960226-G-A

14581881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960227-A-G

14582014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960357-G-C

14582014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960357-G-T

14582084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42960425-C-G

14582329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961071-C-T

http://identifiers.org/hco/4/GRCh38#14582363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42961093-C-A

14582387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961120-T-A

14582548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961265-G-T

http://identifiers.org/hco/4/GRCh38#14582884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42961537-A-C

14582893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961546-C-T

http://identifiers.org/hco/4/GRCh38#14582949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42961602-C-A

14582949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961602-C-T

14582981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961634-A-T

http://identifiers.org/hco/4/GRCh38#14583189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42961837-C-A

14583189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42961837-C-T

14583410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42962077-A-G

14583856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42962470-A-G

http://identifiers.org/hco/4/GRCh38#14584316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42962881-A-C

14586285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42963762-G-T

14586290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42963767-T-A

14586290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42963767-T-C

14586388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42963868-G-T

14586407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42963888-A-T

14595852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42970645-G-A

14595861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42970654-T-A

14596040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42970819-G-A

14596060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42970846-G-C

14596176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42970968-C-T

14596380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42971187-G-T

http://identifiers.org/hco/4/GRCh38#14596625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42971433-C-A

14596865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42971673-T-C

14596886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42971691-T-C

14597166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42971955-G-A

14600078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43000249-C-G

14600259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43000377-G-C

14600498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43000598-T-C

14601216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002219-T-C

14601259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002262-T-C

14601259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002262-T-G

14601293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002296-G-C

14602090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006884-C-T

14602133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006927-T-C

14602277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43007107-A-G

14602373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43007519-C-T

14602417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43007557-A-G

14602873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008003-G-T

14602972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008075-G-T

14611137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010317-A-G

14611138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010318-A-G

14611147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010328-A-G

14611202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010406-G-A

14611310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010493-G-A

14611353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010536-G-T

http://identifiers.org/hco/4/GRCh38#14612214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43015075-C-A

14612227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015083-G-A

14612247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015103-G-T

14612308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015154-A-G

14612571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015399-A-G

14612571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015399-A-T

14612625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015454-G-A

14612733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016215-C-T

14612835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016316-G-A

14612904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016395-A-G

14613074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016563-G-C

14613153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016618-G-A

14613159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016624-T-C

14613171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016636-T-C

14613280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016741-T-G

14613333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016793-T-G

14613487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016938-G-A

14613487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016938-G-T

http://identifiers.org/hco/4/GRCh38#14613591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43017014-C-A

14613612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017035-C-T

14613619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017042-A-G

14613619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017042-A-T

14613641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017063-G-T

14616336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020475-T-C

14616523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020663-T-A

14616644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020792-G-A

http://identifiers.org/hco/4/GRCh38#14616661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43020809-C-A

14617795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43021998-G-A

14621014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43022935-G-A

14621813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023071-C-T

14621884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023146-C-T

14622042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023286-C-T

http://identifiers.org/hco/4/GRCh38#14622061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43023305-A-C

14622354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023602-G-C

14622400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023647-G-A

14622416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023664-A-G

14622439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023687-G-T

14622655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023903-G-A

14622790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43024042-G-T

14625409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43026683-G-A

14625509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43026782-C-G

14625697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43026978-G-A

14625804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43027098-A-G

14625806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43027100-A-G

14626140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43027483-G-C

http://identifiers.org/hco/4/GRCh38#14632468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43028702-C-A

14632531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43028775-A-G

14632593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43028833-T-A

14632593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43028833-T-G

14632826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029064-T-G

14633754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029252-T-C

14633788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029283-C-T

14633802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029297-C-G

http://identifiers.org/hco/4/GRCh38#14633838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43029320-C-A

14633838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029320-C-T

14633929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029388-T-C

14634039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029497-T-A

14634262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029716-G-A

14638947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030665-T-C

14638952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030670-A-G

14638957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030675-A-G

14638974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030692-G-A

14638974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030692-G-C

14638996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030711-T-C

14639070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030785-T-G

14639100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030799-G-C

14639106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030805-A-G

14639106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030805-A-T

14639111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030810-T-C

14640711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031379-T-C

14640784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031424-A-G

14640902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031510-C-T

14641015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031590-C-T

http://identifiers.org/hco/4/GRCh38#14641042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43031616-C-A

14641042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031616-C-T

14641055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031629-A-G

14641208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031792-C-G

14643593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43035975-T-A

14643593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43035975-T-C

14643773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036152-G-C

14643827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036198-G-A

14644037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036425-G-A

14644045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036428-T-G

14644100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036467-G-C

14644270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036593-G-A

14644294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036608-C-G

14644316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036632-C-T

14644661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036977-G-T

14644692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037008-T-C

14644922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037244-T-C

14644957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037273-G-A

14644958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037274-G-C

14645418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037654-G-C

14645720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037999-G-C

14645829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038096-C-T

14645890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038150-A-T

14645901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038161-C-G

http://identifiers.org/hco/4/GRCh38#14646031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43038278-A-C

14646065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038299-A-G

14646303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038621-G-A

14646303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038621-G-T

14646807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43039341-T-C

14648827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43039974-C-T

14648903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040048-G-C

14648932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040077-G-A

14649009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040154-G-A

http://identifiers.org/hco/4/GRCh38#14649221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43040324-A-C

14649263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040374-G-A

14649264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040375-G-A

14649370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040481-G-A

http://identifiers.org/hco/4/GRCh38#14649396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43040502-C-A

14649528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040646-G-A

14650045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040826-C-T

14650154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040975-G-A

14650184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041010-C-G

14650235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041050-G-C

14650319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041126-C-T

14650364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041170-T-C

14650382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041187-C-T

14650444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041249-G-A

14650578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041388-C-T

14650735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041529-T-C

14650803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041598-G-C

14650814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041602-T-C

14650955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041731-T-C

14651158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041919-A-G

14651195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041956-G-A

14651203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041964-C-T

14651260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43042007-T-A

14653307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043190-A-G

14653324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043206-T-G

14653380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043259-C-T

14653482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043336-G-A

14653482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043336-G-C

14653482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043336-G-T

14653543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043386-C-T

14653550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043391-T-G

14653610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043448-G-A

14653622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043458-G-A

14653622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043458-G-C

14653635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043471-T-C

14653897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043733-T-C

14653898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043734-T-G

14653998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043831-G-T

http://identifiers.org/hco/4/GRCh38#14654045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43043873-C-A

14668470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43045136-A-T

http://identifiers.org/hco/4/GRCh38#14668909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43045598-C-A

http://identifiers.org/hco/4/GRCh38#14668981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43045673-A-C

http://identifiers.org/hco/4/GRCh38#14669020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43047296-C-A

14669020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047296-C-G

14669020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047296-C-T

14669050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047323-G-A

14669069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047357-G-A

14669072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047360-C-T

14669425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047671-G-C

14669425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047671-G-T

http://identifiers.org/hco/4/GRCh38#14669446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43047693-C-A

14669481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047728-A-G

14669842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048097-C-T

14669912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048148-C-T

14670125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048258-A-G

14670152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048285-C-T

14670154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048287-C-G

14670184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048313-T-C

14670374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048557-C-G

14670485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048658-C-G

14670489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048662-T-C

14670502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048675-C-T

14670514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048687-A-T

14670520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048693-A-G

14670556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048733-G-T

14670594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048770-G-T

14670678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048850-C-T

14670896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049052-G-A

14670913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049069-T-C

14670913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049069-T-G

14670928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049086-G-T

14670998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049158-C-G

14671163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049305-A-G

14671394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049533-T-C

14671438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049565-G-T

14671442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049569-G-A

http://identifiers.org/hco/4/GRCh38#14671479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43049609-C-A

http://identifiers.org/hco/4/GRCh38#14671739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43049819-C-A

14671755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049835-T-A

14671755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049835-T-C

http://identifiers.org/hco/4/GRCh38#14671756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43049836-C-A

14671756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049836-C-T

http://identifiers.org/hco/4/GRCh38#14671768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43049843-C-A

14671768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049843-C-T

14671791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049850-G-T

14672036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43050068-G-A

14672073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43050105-A-G

14672091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43050124-T-G

14672143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43050171-A-T

14672386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43050385-G-A

http://identifiers.org/hco/4/GRCh38#14673021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43055306-C-A

14673021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43055306-C-T

14673719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43055986-A-G

14673719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43055986-A-T

http://identifiers.org/hco/4/GRCh38#14674428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43056461-A-C

14674428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43056461-A-G

14674481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43056517-C-T

14674609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43056636-T-G

14674639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43056666-A-G

14675135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43057074-C-T

14675247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43057184-G-A

http://identifiers.org/hco/4/GRCh38#14675273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43057210-C-A

14676385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43057988-A-T

14676392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43057995-C-T

http://identifiers.org/hco/4/GRCh38#14676398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43058001-A-C

14676423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058035-G-A

14676525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058135-A-G

14676526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058136-G-A

14676563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058167-T-C

14676702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058323-G-T

14676721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058342-G-C

14676761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43058387-C-G

http://identifiers.org/hco/4/GRCh38#14677469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43059011-C-A

14677469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059011-C-T

14677470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059012-G-A

14677492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059039-A-G

14677501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059048-G-A

http://identifiers.org/hco/4/GRCh38#14677681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43059218-C-A

14677772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059287-T-C

14677999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059512-T-C

14678208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059718-C-T

14678444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43059950-C-G

14678623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060131-G-A

14678676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060185-G-A

14678676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060185-G-T

14678700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060211-G-A

14678761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060272-C-T

14678797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060306-A-G

14678959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060470-T-A

14679117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060643-G-A

14679266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43060785-G-C

http://identifiers.org/hco/4/GRCh38#14682406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43062814-C-A

14682591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43063024-T-C

14682660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43063109-A-G

14682842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43063279-C-G

14682961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43063404-G-A

14683484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43063916-T-A

14683605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064010-A-G

14683847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064216-G-C

14683866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064235-C-T

14684098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064427-G-A

14684098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064427-G-C

14685185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064834-A-T

14685263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43064909-T-G

14685368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065014-G-A

14685456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065095-G-T

14685500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065125-T-C

14685532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065158-G-T

14685537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065163-T-C

14685746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065383-G-A

14685937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065563-C-T

14686069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065730-A-G

14686076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065737-T-C

14686116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065778-G-A

14686335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43065967-C-T

14686606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43066242-T-A

14686622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43066261-C-T

14686736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43066352-G-A

14689349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072345-T-A

14689557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072553-C-T

14689599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072584-T-C

14689637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072622-T-A

14689648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072633-C-T

14689723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072712-G-A

14689723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072712-G-C

14689763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072750-A-G

14689952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072860-T-C

14689954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072862-G-T

http://identifiers.org/hco/4/GRCh38#14689970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43072878-A-C

14689980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43072888-A-G

14690117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073025-T-C

14690152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073056-T-A

14690152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073056-T-C

14690299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073209-C-G

14690525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073424-C-T

14690717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43073637-T-C

14693376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073810-T-A

14693379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073813-G-A

14693392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43073826-G-A

http://identifiers.org/hco/4/GRCh38#14693444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43073897-A-C

14693686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43074132-C-T

14693692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43074138-T-C

14694126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43074566-C-T

14694349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43074974-C-G

14694390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43075015-G-A

14695224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43075920-T-C

http://identifiers.org/hco/4/GRCh38#14695244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43075951-C-A

http://identifiers.org/hco/4/GRCh38#14695279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43075993-A-C

14695311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076025-C-G

14695459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076239-G-T

14695588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076384-A-G

14695629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076401-G-A

14695699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076469-T-A

14695905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076693-T-C

14695930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076718-T-A

http://identifiers.org/hco/4/GRCh38#14696082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43076865-C-A

14696208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43076994-C-T

14696227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077013-C-T

14696513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077360-C-T

http://identifiers.org/hco/4/GRCh38#14696524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43077371-C-A

14697020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077560-T-C

14697053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077594-G-A

14697131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077672-C-G

http://identifiers.org/hco/4/GRCh38#14697205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43077725-C-A

14697449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43077915-A-T

14697596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078019-G-A

14697596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078019-G-T

14697636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078058-G-A

14698045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078230-G-A

14698047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078232-G-T

14698073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078258-C-G

14698073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078258-C-T

14698250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078429-T-C

14698589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078762-T-C

14698725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078892-T-A

14698725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078892-T-G

14698736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078903-A-G

14698832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43078991-T-C

14698932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079091-C-T

14698956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079115-C-T

14698959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079118-C-T

14699078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079242-C-T

14699188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079321-T-C

14699294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079425-T-C

14699455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079599-G-C

14699953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079701-G-T

14700130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079857-T-C

14700190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43079918-G-A

14700539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080274-C-T

14700570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080309-T-A

14700616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080356-G-T

14700632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080370-A-T

14700634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080372-T-A

14700634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080372-T-G

http://identifiers.org/hco/4/GRCh38#14700647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43080385-C-A

14700664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080402-G-A

14700802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080544-T-C

14700947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080679-T-G

14701091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43080872-G-A

14701350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081340-C-G

14701397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081387-G-C

14701430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081420-A-G

14701602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081590-T-A

14701613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081601-C-G

14701863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081810-G-A

14701931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081884-G-A

14701938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43081891-T-C

http://identifiers.org/hco/4/GRCh38#14702098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43082052-C-A

14702098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082052-C-T

14702211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082166-C-T

14702229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082184-T-G

14702346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082317-C-T

14702643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082567-T-C

http://identifiers.org/hco/4/GRCh38#14702684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43082594-C-A

http://identifiers.org/hco/4/GRCh38#14702794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43082710-C-A

14702850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082767-A-G

14702867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082791-G-A

14702867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082791-G-T

14702893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082819-G-A

14702893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082819-G-T

14703010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43082910-C-T

14704914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43086173-C-G

14704914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43086173-C-T

14706176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43092644-T-C

14706439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43092932-A-G

14706483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43092977-T-C

14706588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43093083-A-G

14706594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43093089-T-G

14706661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43093158-G-A

14708488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43094820-G-A

14708841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095291-T-G

14708866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095308-C-G

14709014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095452-T-C

14709033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095471-T-G

http://identifiers.org/hco/4/GRCh38#14709058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43095496-A-C

14709229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095659-A-G

14709301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43095731-C-T

14709650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43096074-T-G

http://identifiers.org/hco/4/GRCh38#14715254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43105206-A-C

14715352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43105284-C-T

14715468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43105326-T-C

14715645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43105895-T-A

14715651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43105901-A-G

14715654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43105904-T-C

14715812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43106071-T-A

14715812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43106071-T-C

14715812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43106071-T-G

14715904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43106126-T-C

14715935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43106165-G-A

http://identifiers.org/hco/4/GRCh38#14716184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43116260-C-A

http://identifiers.org/hco/4/GRCh38#14716259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43116326-C-A

14716359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43116426-T-G

14716458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43116516-T-C

14716495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43116556-T-C

14716526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43116588-A-G

14716690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43116732-G-A

14716692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43116734-G-T

14716777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43116814-C-G

14717079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117117-G-A

14717079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117117-G-C

14717431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117478-A-T

14717495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117544-G-T

14717496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117545-G-A

14718018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117683-T-A

http://identifiers.org/hco/4/GRCh38#14718019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43117684-C-A

14718101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117767-C-G

14718101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117767-C-T

14718166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117820-G-T

14718224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43117883-G-A

14724962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125511-G-A

14725209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125740-A-T

14725267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125793-G-T

14725316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125841-A-G

14725323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125848-G-A

14725323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125848-G-T

14725374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125898-G-T

14725446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43125975-G-A

http://identifiers.org/hco/4/GRCh38#14725448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43125977-C-A

14725564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43126090-C-T

http://identifiers.org/hco/4/GRCh38#14725904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43126912-A-C

14726021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127054-G-A

http://identifiers.org/hco/4/GRCh38#14726261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43127293-A-C

14726449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127464-A-G

14726473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127488-G-A

14726478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127493-T-C

14726501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127514-G-A

14726501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127514-G-C

14726522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127535-G-A

14726773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127794-C-G

14726773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43127794-C-T

14727031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43128051-T-C

14727142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43128154-G-C

14743294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43137992-C-G

14743294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43137992-C-T

14743474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138154-G-C

14743480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138161-T-C

14743622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138302-T-C

14743794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138473-G-A

14743850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138529-G-A

14743967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138647-G-A

14743967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138647-G-C

http://identifiers.org/hco/4/GRCh38#14744040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43138715-A-C

14744346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43138999-C-T

14744347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139000-C-T

14744395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139058-A-G

14744600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139224-G-T

14744609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139233-G-T

14744702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139324-G-A

14744715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139337-G-A

14744715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139337-G-T

14744745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139375-G-T

14744879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139452-G-A

14744949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139483-C-G

14744949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139483-C-T

14744962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139489-T-A

14744962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139489-T-G

14745418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43139882-G-A

14745603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43140078-G-C

14745830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43140298-T-G

14745863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43140331-G-T

14747673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143138-A-G

14749621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143220-C-G

14749621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143220-C-T

14749691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143287-A-G

14749776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143371-C-T

14749816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143412-C-T

http://identifiers.org/hco/4/GRCh38#14749935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43143526-C-A

http://identifiers.org/hco/4/GRCh38#14750000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43143597-C-A

14750046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143643-G-T

14750114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43143709-A-G

14750320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143916-T-A

14750349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43143949-T-C

14750664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43144824-C-T

14750941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43145063-C-G

14751008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43145117-A-G

14751174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43145264-C-G

14762295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43145819-C-T

14762407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43146852-G-C

14762664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43148379-T-C

14762732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43148436-A-T

14764059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43149342-T-C

14767121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43149977-A-G

14767124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43149980-G-C

14767533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43150413-A-G

14767555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43150435-C-T

http://identifiers.org/hco/4/GRCh38#14767721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43150592-C-A

14767830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43150731-A-G

14768317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151263-G-A

14768317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151263-G-C

14768317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151263-G-T

14768380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151323-G-A

14768386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151329-C-G

14768500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151469-G-A

14768542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43151504-G-C

http://identifiers.org/hco/4/GRCh38#14769136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43151917-A-C

14769259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152052-G-C

14769271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152134-T-C

14769272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152135-C-T

14769315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152180-T-C

14769386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152251-G-A

14769430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152294-A-G

14769702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152532-G-C

14769773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152593-C-T

14769804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152624-T-A

14769857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152664-C-T

14770130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43152933-G-A

14770225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43153028-T-C

14770293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43153096-T-C

http://identifiers.org/hco/4/GRCh38#14770324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43153127-C-A

14770324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43153127-C-T

14770392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43153181-T-C

http://identifiers.org/hco/4/GRCh38#14770510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43153259-C-A

14770510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43153259-C-T

14771849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43173815-T-C

http://identifiers.org/hco/4/GRCh38#14771907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#43173874-C-A

14772891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43174808-G-T

14772942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43174859-A-G

14773235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43175186-G-C

14776000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178679-C-T

14776037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178703-T-C

14776218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178865-G-C

14776218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178865-G-T

14776232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178879-G-C

14776265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43178911-C-T

14776686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43179316-G-C

14781239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43179693-G-A

14781567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43179987-A-T

14782467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43180436-A-G

14782914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43181469-T-A

14782982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43181537-T-C

14783057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43181611-A-G

14783360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43181920-T-C

14783442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182008-C-T

14783559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182108-C-G

14783576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182122-C-T

14783696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182248-C-T

14783909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182587-A-G

14784025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182697-G-A

14784025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182697-G-T

14784174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43182888-G-A