39822958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65765215-C-T

39823391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65765609-A-G

39823416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65765633-G-A

http://identifiers.org/hco/4/GRCh38#39823422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65765639-C-A

http://identifiers.org/hco/4/GRCh38#39823474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65765694-C-A

39823474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65765694-C-T

39823820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65765961-T-A

39823932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65766068-G-C

39824216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65766287-T-C

39824387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65766460-T-C

39825043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65767124-T-C

http://identifiers.org/hco/4/GRCh38#39825130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65767208-C-A

39825263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65767338-T-A

39825263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65767338-T-C

39837961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65772703-C-T

39838059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65772801-C-T

http://identifiers.org/hco/4/GRCh38#39838225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65772965-C-A

39838240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772980-A-G

39838891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774896-T-C

39838936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774950-C-T

39839077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775094-T-C

http://identifiers.org/hco/4/GRCh38#39839087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65775104-C-A

39839087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775104-C-T

39839133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775145-A-T

39844304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776651-G-A

39844304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776651-G-C

http://identifiers.org/hco/4/GRCh38#39844518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65776825-A-C

39844613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776913-A-G

http://identifiers.org/hco/4/GRCh38#39845173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65777270-A-C

39845272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777353-A-G

39845525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777644-T-C

39845570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777703-T-C

39845703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777816-G-A

39848594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65780124-T-A

39848594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65780124-T-G

http://identifiers.org/hco/4/GRCh38#39848613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65780138-C-A

http://identifiers.org/hco/4/GRCh38#39848734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65780203-C-A

http://identifiers.org/hco/4/GRCh38#39848735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65780204-C-A

39848735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65780204-C-T

39849075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65780527-T-C

http://identifiers.org/hco/4/GRCh38#39849114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65780560-C-A

39849400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781075-T-A

39849400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781075-T-C

39849400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781075-T-G

39849723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781465-T-A

39862299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65784508-A-G

39862939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65784973-G-A

39862939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65784973-G-C

39862954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65784988-C-T

39863242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65785252-A-G

39863242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65785252-A-T

http://identifiers.org/hco/4/GRCh38#39863519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65785522-C-A

39863519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65785522-C-T

http://identifiers.org/hco/4/GRCh38#39863614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65785602-A-C

39866756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787180-T-A

39866756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787180-T-C

39866779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787203-G-T

39867085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787487-T-C

39867106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787507-T-G

39867142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787543-T-C

39867258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65787734-C-T

39867846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65788370-C-T

39869083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65788692-A-G

39869359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65789021-A-G

39869359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65789021-A-T

39872925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65791454-T-G

http://identifiers.org/hco/4/GRCh38#39873187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65791714-A-C

39873187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65791714-A-G

http://identifiers.org/hco/4/GRCh38#39873245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65791752-C-A

39873245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65791752-C-T

39874121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65792508-G-C

http://identifiers.org/hco/4/GRCh38#39874201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65792585-C-A

http://identifiers.org/hco/4/GRCh38#39874229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65792611-C-A

39874229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65792611-C-T

39874445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65792814-T-G

http://identifiers.org/hco/4/GRCh38#39874496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65792860-A-C

http://identifiers.org/hco/4/GRCh38#39874524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65792888-C-A

39874524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65792888-C-G

39874583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65792939-T-A

39874677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793013-C-T

39874703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793039-C-G

39874996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793309-T-C

39875010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793321-C-G

39875093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793413-A-G

39875873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65793967-T-C

http://identifiers.org/hco/4/GRCh38#39876450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65794641-C-A

39876450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65794641-C-T

39877266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795360-T-G

http://identifiers.org/hco/4/GRCh38#39879648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65795820-C-A

39879648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795820-C-T

39879676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795847-G-A

39879676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65795847-G-T

39879844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796015-A-G

39879851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796022-T-C

http://identifiers.org/hco/4/GRCh38#39879893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65796068-C-A

39879919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796089-T-A

39879976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796141-T-C

http://identifiers.org/hco/4/GRCh38#39880009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65796175-C-A

39880078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796244-A-G

39880124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796294-T-C

http://identifiers.org/hco/4/GRCh38#39890035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65801175-A-C

39890089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801228-A-G

39890116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801252-T-G

http://identifiers.org/hco/4/GRCh38#39890126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65801263-C-A

39890126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801263-C-G

39890174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801311-G-A

39890174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801311-G-T

39890382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801494-T-A

39890382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801494-T-C

39890400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801504-T-C

39890400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801504-T-G

39890416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801527-G-A

39890416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801527-G-T

http://identifiers.org/hco/4/GRCh38#39890510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65801619-C-A

39890510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801619-C-T

39890568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801681-A-G

39890589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801693-C-T

39897956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803247-G-C

39897956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803247-G-T

http://identifiers.org/hco/4/GRCh38#39898173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65803465-A-C

39898173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65803465-A-G

http://identifiers.org/hco/4/GRCh38#39898253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65803554-A-C

39898253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65803554-A-G

http://identifiers.org/hco/4/GRCh38#39898270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65803571-A-C

39898270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65803571-A-G

39898323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65803613-G-T

39898361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 65803647-G-T

39898398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65803685-A-G

39898479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65803766-G-A

39898755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804409-G-C

39898755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804409-G-T

http://identifiers.org/hco/4/GRCh38#39898894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65804526-A-C

39898894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804526-A-T

39898964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804591-G-A

39898964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804591-G-T

39899058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804707-G-A

http://identifiers.org/hco/4/GRCh38#39900328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65805178-C-A

http://identifiers.org/hco/4/GRCh38#39900339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65805190-C-A

http://identifiers.org/hco/4/GRCh38#39900468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65805309-C-A

39900468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65805309-C-T

http://identifiers.org/hco/4/GRCh38#39900571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65805406-A-C

39902312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65807702-T-C

39902323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65807713-G-C

39902323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65807713-G-T

39902327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65807717-T-C

http://identifiers.org/hco/4/GRCh38#39902364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65807753-C-A

39902364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65807753-C-T

39902366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65807755-A-G

39902418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65807807-G-T

39904269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65808705-T-A

39904269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65808705-T-C

39908440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65809776-A-G

39908440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65809776-A-T

39908609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65809939-G-T

39909941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65811191-A-T

39910098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65811230-G-A

http://identifiers.org/hco/4/GRCh38#39910154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65811282-C-A

39910154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65811282-C-T

39910166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65811294-G-A

39910166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65811294-G-T

39910236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65811340-T-A

39910236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65811340-T-C

http://identifiers.org/hco/4/GRCh38#39910257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65811361-C-A

39910257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65811361-C-T

39913464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65811967-T-G

39913580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65812095-A-G

39913616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65812137-A-G

39913616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65812137-A-T

39913679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65812200-T-C

39913697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65812218-A-G

39913734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65812255-G-A

39913734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65812255-G-T

39913792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812304-A-G

39913841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812313-G-T

39913849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812321-T-A

http://identifiers.org/hco/4/GRCh38#39913853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65812325-A-C

39913853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812325-A-G

39913853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812325-A-T

http://identifiers.org/hco/4/GRCh38#39913877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65812349-A-C

39915755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812893-G-T

39915839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812976-T-G

39915903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813042-A-G

39917086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65813649-A-G

39917343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813899-T-G

http://identifiers.org/hco/4/GRCh38#39920155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65815529-A-C

http://identifiers.org/hco/4/GRCh38#39920203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65815571-C-A

39920548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815876-T-C

http://identifiers.org/hco/4/GRCh38#39922510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65816850-C-A

39922510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65816850-C-T

39922847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65817464-T-C

39922881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65817504-T-C

39922882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65817505-G-A

http://identifiers.org/hco/4/GRCh38#39926699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65821709-C-A

39926699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65821709-C-T

39926805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65821801-T-C

39926829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65821825-T-C

39926838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65821834-T-C

39926890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65821894-G-A

39926890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65821894-G-C

39926890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65821894-G-T

39926922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65821937-T-C

39927126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65822131-T-C

39927405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65822366-T-C

39927679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65823279-G-A

39927703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65823297-T-A

39927792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65823356-T-C

39927835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65823377-T-G

39927912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65823436-G-T

39974381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65851017-G-T

39975286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65852573-A-G

39975468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65852708-A-G

39975621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853340-C-G

39975626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853345-T-C

http://identifiers.org/hco/4/GRCh38#39975686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65853390-C-A

39975831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853512-C-G

39976045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853711-T-A

39976045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853711-T-C

39976045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65853711-T-G

39976168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65853849-T-C

39976168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65853849-T-G

39976313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65853968-A-T

http://identifiers.org/hco/4/GRCh38#39976347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65854004-C-A

39976347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65854004-C-G

http://identifiers.org/hco/4/GRCh38#39976464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65854130-C-A

39976464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65854130-C-G

39976464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65854130-C-T

39976584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65854247-G-A

39976584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65854247-G-C

39976595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65854258-G-T

39977218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65854862-C-T

39977315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65854959-C-T

39977438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65855078-G-A

39977438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65855078-G-C

39977455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: 65855091-A-G

http://identifiers.org/hco/4/GRCh38#39977697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65855335-C-A

39977697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5 prime UTR variant
orthologous variants: 65855335-C-T

39977863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5 prime UTR variant
orthologous variants: 65855521-G-A

http://identifiers.org/hco/4/GRCh38#39977888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29088
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#65855550-C-A