68054645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887831-G-A

68054645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887831-G-T

68054659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 62887817-G-A

68054659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 62887817-G-T

68054678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887798-A-G

http://identifiers.org/hco/15/GRCh38#68054680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#62887796-C-A

68054680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 62887796-C-T

http://identifiers.org/hco/15/GRCh38#68054688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#62887784-C-A

68054688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 62887784-C-T

68054858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887606-T-G

68054867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887597-C-G

http://identifiers.org/hco/15/GRCh38#68054942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62887533-C-A

68054942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887533-C-T

68054947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62887528-G-T

68055984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62886380-T-C

68055997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62886235-T-C

68056623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62885274-G-A

68057146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62884797-C-T

68057190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62884761-T-C

68057496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 62883740-G-A

68057496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 62883740-G-T

68057543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 62883699-G-A

68057543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 62883699-G-T

68057581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 62883658-G-C

68058006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62883273-C-T

68058606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62882470-C-G

68060705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62880468-A-G

68060705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62880468-A-T

http://identifiers.org/hco/15/GRCh38#68061130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62880150-A-C

68061609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62879610-T-A

68061610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62879609-G-C

68062063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62879004-A-G

68062074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62878993-A-G

68063733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62876705-C-T

68064373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62875864-A-G

68064392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62875846-C-T

68066753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62873572-G-A

68078314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62869853-G-T

68078315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62869852-C-T

68078590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62869598-G-A

68078590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62869598-G-C

68079230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62868126-G-A

68079325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62868037-A-G

68083638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62863207-A-T

68084572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62861076-A-G

68084668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62861020-C-G

68084668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62861020-C-T

68085004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62860714-T-C

68085004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62860714-T-G

68086188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62859584-G-C

68086576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859210-T-C

68086591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859195-G-T

68086612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859174-G-A

68086612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859174-G-C

68086627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859159-C-G

68086627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 62859159-C-T

68086776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62859012-G-T

68086777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62859011-G-T

68087265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62858479-C-G

68087265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62858479-C-T

68087734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62857685-A-G

68087816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62857065-A-G

68087832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62857049-T-C

68087863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62857019-A-G

68087959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62856187-C-G

68088390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62855298-T-G

68088419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62855269-C-G

68088724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62855014-A-G

68089078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62854578-T-C

68094563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62852733-C-T

68094624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62852677-T-C

68094625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62852676-C-G

http://identifiers.org/hco/15/GRCh38#68094627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62852674-A-C

68094693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62852611-C-G

68094781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62852547-C-G

http://identifiers.org/hco/15/GRCh38#68095175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62852206-C-A

68108610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62845374-T-G

68108971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844900-G-A

68109330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844471-G-A

68109341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844460-C-G

68109447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844382-T-C

68109809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844041-A-G

68109854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62844001-A-G

68109916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62843935-G-A

68113451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62842225-A-T

68113749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62841989-T-C

68113749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62841989-T-G

68114404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62840656-T-G

68114799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62840291-C-G

68114848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62840247-T-A

68140920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62832134-T-C

68141243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62831651-A-G

68141318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62831575-C-T

http://identifiers.org/hco/15/GRCh38#68141809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62831046-C-A

68141809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62831046-C-T

http://identifiers.org/hco/15/GRCh38#68141894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62830983-C-A

68141894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830983-C-G

68141894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830983-C-T

68141904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830973-G-A

68141904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830973-G-T

68142156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830767-T-C

68142172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830701-G-A

68142172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830701-G-T

68142253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62830641-T-C

68142365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62830533-A-G

68142543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62830462-T-C

http://identifiers.org/hco/15/GRCh38#68142626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62830390-C-A

68142626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62830390-C-G

68142626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62830390-C-T

68145305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62829564-T-G

68145335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62829534-G-A

68145424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62829458-G-A

68145920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827724-G-A

68145940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827704-G-T

68146031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827571-G-T

68146032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827570-A-G

68146032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827570-A-T

http://identifiers.org/hco/15/GRCh38#68146044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62827558-A-C

68146062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827548-C-G

68146146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827465-C-T

68146162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827449-A-G

68146212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62827404-T-G

68146368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62826951-C-T

68146721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826610-A-G

68146766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826566-T-C

http://identifiers.org/hco/15/GRCh38#68146843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62826492-C-A

68146843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826492-C-T

68146888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826487-G-T

68146893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826482-T-G

68147019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826365-G-A

68147019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62826365-G-T

68147497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62825945-T-C

68147652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62825821-A-G

68148008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62825485-C-G

http://identifiers.org/hco/15/GRCh38#68148041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62825450-A-C

68148041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62825450-A-G

68148310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62825192-G-A

68150214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62823083-G-T

68150389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62822640-A-G

68150601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62822229-G-C

68150601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62822229-G-T

68151342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62821812-C-G

68151342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62821812-C-T

68151441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62821687-A-G

68152599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62821047-G-A

http://identifiers.org/hco/15/GRCh38#68152612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62821040-C-A

68152612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62821040-C-T

68152678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62820980-A-G

68152767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62820909-T-G

68153993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62819669-A-G

68154051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62819605-T-C

68154395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62819225-G-A

68154421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62819198-C-T

68154634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818928-C-T

68154751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818806-G-A

68154809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818730-C-T

68154840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818699-G-A

68155132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818431-C-T

68155410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818101-T-A

68155468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62818031-A-G

http://identifiers.org/hco/15/GRCh38#68155527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62817930-C-A

68155561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62817860-A-G

68156379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62817188-A-G

68156379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62817188-A-T

68157105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816744-A-G

68157172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816687-G-T

68157218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816645-G-A

http://identifiers.org/hco/15/GRCh38#68157320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62816549-C-A

68157329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816540-G-A

68157329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816540-G-T

68157343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62816526-A-G

68158141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815794-A-G

http://identifiers.org/hco/15/GRCh38#68158437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62815628-A-C

68158592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815483-T-G

68158869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815182-T-A

68158938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815118-G-A

68158986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815068-G-A

68158986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62815068-G-C

68161549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62813172-C-T

68161553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62813168-T-G

http://identifiers.org/hco/15/GRCh38#68162188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62812740-C-A

68162188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62812740-C-T

68163364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62811836-G-A

68163655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62811377-A-G

68163655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62811377-A-T

68163662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62811370-T-G

68163718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62811343-G-A

68164408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62810419-G-C

68164424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62810404-G-A

68164424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62810404-G-C

68164424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62810404-G-T

68165710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62808949-A-G

68166443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807931-G-T

68166521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807860-G-A

68166550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807831-G-A

68166575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807801-C-T

68166643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807734-T-C

68167259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807409-G-A

68167519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807138-T-C

68167540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62807117-T-C

68168641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62806659-C-T

68168696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62806608-T-C

68168819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62806470-G-A

68168877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62806415-G-A

68171831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62804718-T-G

68172906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62804389-C-T

68172936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62804366-T-G

68173370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62804055-A-T

http://identifiers.org/hco/15/GRCh38#68173380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62804045-A-C

68173623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62803377-T-C

68173647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62803353-A-G

68173647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62803353-A-T

http://identifiers.org/hco/15/GRCh38#68173659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62803341-C-A

68173680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62803320-T-G

68173864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: missense variant
orthologous variants: 62803139-G-A

68173864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: missense variant
orthologous variants: 62803139-G-T

68173927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62803087-T-C

68175000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62801449-A-G

68175190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62801222-T-A

68175244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62801115-G-T

68175454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62800916-T-G

http://identifiers.org/hco/15/GRCh38#68175612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62800554-C-A

68175612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62800554-C-G

68175612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62800554-C-T

http://identifiers.org/hco/15/GRCh38#68175653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62800523-C-A

68175653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: synonymous variant
orthologous variants: 62800523-C-T

68175761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: missense variant
orthologous variants: 62800415-G-A

68176432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron variant
orthologous variants: 62799618-A-G

68176506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: missense variant
orthologous variants: 62799554-G-A

68176765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62799308-A-G

68176798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62799282-G-T

68176800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62799280-A-G

68176801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62799279-A-G

68176822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62799258-A-G

68178738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62797306-G-C

68178738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62797306-G-T

68178772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62797278-T-G

68179038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62797036-T-A

68179238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796851-C-G

68179509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796624-G-T

68180918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795100-T-C

68180924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795094-G-A

68180946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795074-G-A

68181086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794864-T-G

68181087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794863-T-C

68181090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794860-T-A

68181090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794860-T-C

http://identifiers.org/hco/15/GRCh38#68181143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62794792-C-A

68181143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794792-C-T

68181428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 62794518-G-T

68181483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794484-G-T

68181575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794409-T-C

68181608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794377-G-C

68181608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794377-G-T

68181652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794337-T-C

68181709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794271-T-C

68181753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794216-A-G

http://identifiers.org/hco/15/GRCh38#68181792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62794169-C-A

68181792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794169-C-G

68181792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62794169-C-T

68182237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62793748-T-G

http://identifiers.org/hco/15/GRCh38#68183480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62792697-A-C

68183499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62792217-A-G

http://identifiers.org/hco/15/GRCh38#68183536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62792181-A-C

68183536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62792181-A-G

68183676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62792041-T-A

68183676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62792041-T-C

68184065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791621-A-G

http://identifiers.org/hco/15/GRCh38#68184172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62791528-A-C

68184172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791528-A-T

68184302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791408-G-T

68184353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791372-T-A

68184353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791372-T-C

68184478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62791249-C-G

68187946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 62789143-T-A

68187946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 62789143-T-C

68188266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788830-G-T

68188340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788757-A-G

68188340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788757-A-T

68188447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788632-G-T

68188657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788459-G-A

68189129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62788006-T-A

68189276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62787866-A-G

68189379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62787762-T-C

68189568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62787571-A-G

68189727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62787419-C-T

68189932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62787208-G-C

68190275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 62786856-T-C

http://identifiers.org/hco/15/GRCh38#68190493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62786661-C-A

68190493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant
orthologous variants: 62786661-C-T

68191508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62785602-A-G

http://identifiers.org/hco/15/GRCh38#68191550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62785560-C-A

68191550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62785560-C-T

68191551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62785559-C-G

http://identifiers.org/hco/15/GRCh38#68191643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62785496-C-A

68191907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62785272-G-T

68191940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62785243-C-T

68191981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62785202-C-T

68192141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62784684-T-C

68192155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 62784672-T-A

68192267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62784570-G-A

68192267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62784570-G-C

68192267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62784570-G-T

http://identifiers.org/hco/15/GRCh38#68192276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62784561-C-A

68192276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62784561-C-T

68192324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62784514-G-T

68192562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62784192-A-G

68192763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783997-T-C

68192763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783997-T-G

68192877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783906-T-C

68193196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783716-G-T

68193243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783667-T-C

68193476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783406-T-C

68193745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783083-G-C

68193745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783083-G-T

68193785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783043-G-A

68193785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62783043-G-T

68193843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62782989-T-A

68193949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62782928-A-G

68193949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62782928-A-T

68193989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62782890-A-G

http://identifiers.org/hco/15/GRCh38#68194023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62782846-C-A

68194073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62782796-C-T

68194264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62782641-G-T

68194279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62782630-G-A

http://identifiers.org/hco/15/GRCh38#68194331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62782591-C-A

68197247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62778868-C-T

68197398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62778760-T-G

http://identifiers.org/hco/15/GRCh38#68198434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62777392-C-A

68198434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62777392-C-G

http://identifiers.org/hco/15/GRCh38#68198494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#62777333-C-A

68198496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62777331-T-C