68560452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 62723079-C-T

68560650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62722880-G-T

68560681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62722849-G-T

http://identifiers.org/hco/10/GRCh38#68560726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62722803-A-C

68560726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62722803-A-G

68560726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62722803-A-T

68560766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62722763-G-A

68560795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62722737-G-A

68560816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62722718-G-A

http://identifiers.org/hco/10/GRCh38#68560863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62722674-C-A

68560863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62722674-C-T

68560946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62722600-G-A

68561208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62722374-C-T

68561548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62722135-C-T

68561557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62722126-G-A

68562722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62720518-A-G

68562722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62720518-A-T

68563057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62720225-C-T

68563255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62720043-T-C

http://identifiers.org/hco/10/GRCh38#68563332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62719993-C-A

http://identifiers.org/hco/10/GRCh38#68563437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62719862-A-C

68563437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62719862-A-G

68563600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62719712-C-T

68563628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62719686-A-G

http://identifiers.org/hco/10/GRCh38#68563658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62719656-C-A

68565669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62717929-C-T

68566166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62717437-G-T

68572125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62716021-T-A

68572126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62716020-A-G

68572307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62715823-T-C

http://identifiers.org/hco/10/GRCh38#68572331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62715799-C-A

68572331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62715799-C-T

68572354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715776-C-T

68572567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715566-G-C

68572701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62715432-C-G

68572701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62715432-C-T

68572720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715413-G-A

68572720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715413-G-C

68572720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715413-G-T

68572795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715353-T-G

http://identifiers.org/hco/10/GRCh38#68572824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62715324-C-A

68572824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62715324-C-T

68572937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62715208-A-T

http://identifiers.org/hco/10/GRCh38#68573385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62714790-C-A

68573385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62714790-C-G

68573385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62714790-C-T

68573491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62714669-C-T

68573682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62714496-A-G

68573702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62714476-C-G

68573950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62714228-C-T

68574020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62714161-T-C

68574081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62714100-G-A

68574106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 62714075-C-T

68578092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62713172-T-C

68578301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62712962-C-T

68578352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62712921-G-A

68578352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62712921-G-T

68587219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62708432-T-A

68587257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62708382-C-T

68587280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62708353-G-A

http://identifiers.org/hco/10/GRCh38#68587281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62708352-A-C

68587355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62708279-G-C

68587469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62708182-C-T

68596792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62704172-G-A

68596888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62704086-T-C

68596901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62704073-C-G

68596901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62704073-C-T

68597359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62703996-T-C

68599162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62702591-G-A

68599163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62702590-G-A

68599283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62702475-G-A

http://identifiers.org/hco/10/GRCh38#68599287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62702471-A-C

68599462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62702284-G-A

68599569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62702181-T-C

68599796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62701917-A-T

http://identifiers.org/hco/10/GRCh38#68600331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62701384-A-C

68600331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62701384-A-G

68600334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62701381-G-A

68600855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62700841-G-A

68600925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700754-G-T

68601102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700509-G-C

68601102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700509-G-T

68601103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700508-G-T

68601132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700479-C-T

68601197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700414-G-T

68601248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700377-A-T

68601518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62700097-T-C

68602195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62699449-T-C

68602875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62697796-T-G

68603055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62697645-T-C

68603155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62697545-T-C

68603166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62697537-T-G

68603527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62697101-T-A

68605160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62695356-A-G

68606880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62693511-C-T

http://identifiers.org/hco/10/GRCh38#68607141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62693108-C-A

68607141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62693108-C-G

68607141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62693108-C-T

68607289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62692529-G-A

68624156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62684191-T-G

68624253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62684027-T-C

68624254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62684026-G-A

68624254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62684026-G-C

68624415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62683801-G-A

68624445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62683772-A-G

68644681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62676176-A-G

68644860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675990-A-T

68645038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675809-C-G

68645154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675693-A-G

68645154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675693-A-T

68645277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675576-C-T

68645361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675492-T-G

68645466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675387-T-A

68645801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62675133-G-A

68645890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62675047-G-A

68646051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62674892-G-A

68646134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62674809-T-A

68646134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62674809-T-C

68646163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62674783-C-G

68646181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62674765-A-T

68646840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62674106-A-T

68647153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673841-T-A

68651586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62669585-T-C

68651717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62669481-A-T

http://identifiers.org/hco/10/GRCh38#68651953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62669298-C-A

68651997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62669256-A-G

http://identifiers.org/hco/10/GRCh38#68652086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62669178-C-A

68652086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62669178-C-T

68652161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62669116-C-T

68652371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668909-T-A

68652371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668909-T-G

68652451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668812-T-A

68652480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668784-T-C

68652480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668784-T-G

68652521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62668744-C-T

http://identifiers.org/hco/10/GRCh38#68667186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62658396-A-C

http://identifiers.org/hco/10/GRCh38#68667195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62658387-A-C

http://identifiers.org/hco/10/GRCh38#68667277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62658305-C-A

68667277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62658305-C-T

68672917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62655378-A-G

68673159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62655168-A-G

68673281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62655082-G-T

68673300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62655068-G-A

68673300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62655068-G-T

http://identifiers.org/hco/10/GRCh38#68673364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62655003-C-A

68673364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62655003-C-T

68681087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62652483-C-T

68681301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62652312-T-C

68681379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62652270-T-A

68681379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: intron variant
orthologous variants: 62652270-T-C

68681468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62652181-C-T

68682959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62650227-A-G

68686401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62649559-C-T

68691320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62648756-G-A

68691320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62648756-G-C

68691785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62648338-G-A

68691785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62648338-G-T

http://identifiers.org/hco/10/GRCh38#68691800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62648323-A-C

68691800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: missense variant
orthologous variants: 62648323-A-G

68691824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648299-T-A

68691927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648155-G-A

68691927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648155-G-T

68691941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648145-A-G

68691941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648145-A-T

68691962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648126-G-A

68691962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648126-G-T

68692002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62648088-A-T

68692151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647955-T-G

68692153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647952-T-G

68692175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647930-G-A

68692175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647930-G-C

68692175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647930-G-T

68692272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647833-A-T

68692301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647804-G-A

68692301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647804-G-T

68692394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647712-G-T

http://identifiers.org/hco/10/GRCh38#68692536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62647567-C-A

68692682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647475-T-C

http://identifiers.org/hco/10/GRCh38#68692704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62647456-A-C

http://identifiers.org/hco/10/GRCh38#68692708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62647452-C-A

68692708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647452-C-T

http://identifiers.org/hco/10/GRCh38#68692726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62647438-C-A

68692747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647418-T-A

68692898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647294-A-T

68692998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647216-G-A

68692998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647216-G-T

68693025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647199-G-T

68693079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647163-A-G

http://identifiers.org/hco/10/GRCh38#68693111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62647131-C-A

68693111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647131-C-T

68693231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62647016-G-T

68693254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646991-A-G

68693305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646952-C-T

68693312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646944-A-G

http://identifiers.org/hco/10/GRCh38#68693323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62646933-C-A

68693336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646915-A-G

68693337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646914-G-A

http://identifiers.org/hco/10/GRCh38#68693479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62646778-C-A

http://identifiers.org/hco/10/GRCh38#68693503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62646761-C-A

http://identifiers.org/hco/10/GRCh38#68693567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62646693-C-A

68693660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646609-T-G

68693706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646582-A-G

http://identifiers.org/hco/10/GRCh38#68693821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62646466-A-C

68693829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646464-C-T

68693914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646393-C-T

68693921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646386-T-C

68694308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62646012-G-T

http://identifiers.org/hco/10/GRCh38#68694349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62645973-C-A

68694349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62645973-C-T

68694429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29484
most severe consequence: 3 prime UTR variant
orthologous variants: 62645829-G-A