http://identifiers.org/hco/5/GRCh38#14581890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27681615-C-A

14581890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27681615-C-G

14581890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27681615-C-T

14581918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 27681601-G-A

14581918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 27681601-G-T

14581920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27681599-G-A

14581920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27681599-G-C

14581920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27681599-G-T

14582001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681555-G-A

14582001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681555-G-T

14582320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681323-C-T

14582376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681275-C-G

14582454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681202-G-A

14582454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681202-G-C

http://identifiers.org/hco/5/GRCh38#14582557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27681159-A-C

http://identifiers.org/hco/5/GRCh38#14583213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27680760-C-A

14583306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680646-T-A

14583434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680525-C-T

14583535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680426-C-T

14583593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680368-G-A

14583659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680300-A-T

14584013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679792-T-C

14584026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679781-G-A

14584044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679762-C-G

14584197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679633-C-T

14584239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679586-T-A

14584261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679558-T-C

http://identifiers.org/hco/5/GRCh38#14584296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27679523-C-A

14584296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679523-C-G

14584329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679489-C-T

14584412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679369-A-G

14584473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679330-C-G

14584473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679330-C-T

14584751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679050-A-G

14584797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679004-G-A

http://identifiers.org/hco/5/GRCh38#14584825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27678977-A-C

14584825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27678977-A-G

14585055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27678769-T-C

http://identifiers.org/hco/5/GRCh38#14585230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27678639-A-C

14585286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27678577-A-G

http://identifiers.org/hco/5/GRCh38#14585720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27678139-A-C

14585779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27678080-A-G

14585839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27678018-G-A

14585873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677987-G-A

14586072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677788-A-G

http://identifiers.org/hco/5/GRCh38#14586101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27677761-A-C

14586398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677359-A-T

14586514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677246-A-G

14586517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677243-C-G

14586892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676776-G-C

14587067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676628-G-T

14587132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676563-C-G

14587139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676556-C-T

14587150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676545-G-A

14587527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676201-C-G

14587663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676066-G-T

14587695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676041-T-C

14587696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676040-A-G

14587891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675889-T-C

14588020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675786-C-T

14588191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675613-A-G

14588195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675609-C-G

14588299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675501-T-C

14588299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675501-T-G

14588498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675317-G-A

14588504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675310-T-G

14588707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675092-A-G

14588981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674646-C-T

14589096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674527-G-A

14589096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674527-G-C

14589096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674527-G-T

14589211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674432-G-T

14590029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673592-G-A

14590189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673453-G-A

http://identifiers.org/hco/5/GRCh38#14590261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27673387-A-C

14590350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673259-G-A

14590532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673106-T-A

14590532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673106-T-G

14590533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673105-G-A

14590642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673014-C-T

14590743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672935-T-A

14591014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672700-C-T

14591031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672683-A-G

14591070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672645-G-T

http://identifiers.org/hco/5/GRCh38#14591096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27672619-C-A

14591098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672612-A-G

14591108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672577-G-A

14591121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672564-A-G

14591250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672434-A-T

14591440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672254-A-G

14591566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27672171-G-A

http://identifiers.org/hco/5/GRCh38#14591587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27672150-C-A

http://identifiers.org/hco/5/GRCh38#14592902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27672101-C-A

14592952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672053-C-T

14592991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672020-T-C

14593154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671913-A-G

14593248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671833-T-C

14593251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671830-C-T

14593284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671797-C-G

14593538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671337-G-A

14593561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671314-G-A

14593599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671277-C-T

http://identifiers.org/hco/5/GRCh38#14593726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27671151-C-A

14593820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671068-T-G

14593882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671012-A-G

http://identifiers.org/hco/5/GRCh38#14595061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27670718-A-C

http://identifiers.org/hco/5/GRCh38#14595080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27670700-A-C

14595091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670689-G-A

http://identifiers.org/hco/5/GRCh38#14595186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27670610-C-A

14595439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670260-G-T

14595483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27670215-G-A

14595751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669983-T-C

14596655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668520-G-A

14596655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668520-G-C

14597085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668447-A-G

14597136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668392-G-A

14597203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668326-G-C

14597246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668287-A-G

14597299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668253-G-A

14597325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668231-C-T

14597501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668117-T-C

14597696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667961-G-A

http://identifiers.org/hco/5/GRCh38#14597739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27667916-A-C

14597752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667903-C-T

14597838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667817-A-T

14597849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667806-T-C

14597955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667344-G-A

14598026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667285-G-T

14598069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667251-C-G

14598069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667251-C-T

14598158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667156-G-T

14598214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667093-A-G

14598245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667074-C-T

http://identifiers.org/hco/5/GRCh38#14598450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27666858-A-C

14598532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27666766-G-A

14599765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665876-G-T

14599856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665788-T-C

14599967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665716-T-C

http://identifiers.org/hco/5/GRCh38#14600846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27664992-C-A

14600874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27664965-A-T

14600992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27664870-T-C

14601059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27664803-A-G

14601066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27664796-G-A

14601066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27664796-G-T

14601073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27664789-C-T

14601171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27664693-C-G

14601171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27664693-C-T

14601418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27664452-A-G

14601419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27664451-C-G

14601419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27664451-C-T

14601482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27664399-G-T

http://identifiers.org/hco/5/GRCh38#14601548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27664333-A-C

14601587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27664301-G-A

14601654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663862-G-A

14601654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663862-G-C

14601876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663647-T-C

14601919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663611-T-C

14602193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27662562-A-G

14602401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662377-T-C

14602401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662377-T-G

14602427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662347-T-C

14602593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662278-G-A

http://identifiers.org/hco/5/GRCh38#14602987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27662104-C-A

14602987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662104-C-T

14603020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662062-T-A

14603458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661613-A-G

14603508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661561-T-C

14603513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661556-T-G

14603616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661304-T-C

14603675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661244-T-A

14603679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661240-T-C

14603913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660821-T-C

14603923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660811-T-G

http://identifiers.org/hco/5/GRCh38#14603932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27660802-C-A

14603932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660802-C-G

14606864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660269-G-A

14607538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659879-G-A

14607659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659774-C-G

14607659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659774-C-T

14607672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659759-C-G

14607699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659733-G-A

14607699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659733-G-C

14607865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659579-A-G

14608040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659415-G-A

14608087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659367-G-A

14608087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659367-G-T

14608097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659357-T-C

14608166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659288-T-A

14608168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659286-T-C

14608688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658734-T-C

14608693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658729-T-C

14608698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658601-T-A

14608698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658601-T-C

http://identifiers.org/hco/5/GRCh38#14608699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27658600-A-C

14608699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658600-A-G

14608701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658598-G-A

http://identifiers.org/hco/5/GRCh38#14608703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27658550-C-A

14608703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658550-C-T

14608789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27658357-A-T

14608880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27658266-G-A

14609893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657399-C-T

14609939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657341-A-G

14609939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657341-A-T

14610014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657267-G-A

14610014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657267-G-T

14610019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657262-T-A

14610019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657262-T-C

14610019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657262-T-G

14610095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657201-A-G

http://identifiers.org/hco/5/GRCh38#14610112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27657184-C-A

14610112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657184-C-T

14610222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27657074-G-A

http://identifiers.org/hco/5/GRCh38#14610303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27656993-C-A

14610420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 27656875-G-T

14610490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656834-G-A

14610490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656834-G-T

14610536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656803-T-A

14610536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656803-T-C

14610536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656803-T-G

14610590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656761-G-A

14610603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656748-T-A

http://identifiers.org/hco/5/GRCh38#14610667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#27656711-A-C

14610670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656708-A-G

14610830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656543-G-A

14610901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656475-T-C

14610901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656475-T-G

14610991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656397-G-C

14610991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656397-G-T

14611059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656323-T-C

14611127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656243-C-T

14611142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656228-T-A

14611162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25629
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27656215-G-A