100083767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116424383-C-T

http://identifiers.org/hco/1/GRCh38#100083984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116424196-C-A

100084467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116423652-T-A

100084918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422788-A-G

100085007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422720-G-A

100085007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422720-G-T

100085076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422676-A-G

100085196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422573-T-C

100085201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422568-G-T

100085247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422539-G-A

100085247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116422539-G-C

http://identifiers.org/hco/1/GRCh38#100085330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422459-A-C

100085365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422424-G-A

100085413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422376-A-G

100085450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422342-A-G

100085453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422339-A-G

http://identifiers.org/hco/1/GRCh38#100085461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422325-C-A

100085485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422312-A-G

100085525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422270-T-G

100085545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422250-T-C

http://identifiers.org/hco/1/GRCh38#100085550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422245-A-C

http://identifiers.org/hco/1/GRCh38#100085565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422230-C-A

100085568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422227-C-G

100085568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422227-C-T

100085590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422205-T-C

100085606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116422189-G-T

http://identifiers.org/hco/1/GRCh38#100085620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422175-C-A

100085620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116422175-C-T

100085646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422148-G-A

100085646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422148-G-T

http://identifiers.org/hco/1/GRCh38#100085696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116422109-A-C

100085713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422092-A-T

http://identifiers.org/hco/1/GRCh38#100085888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116421933-A-C

100088081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420874-T-C

100088123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420831-G-A

100088123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420831-G-T

100088124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420830-T-A

100088124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420830-T-C

100088134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420819-C-T

100088196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116420760-A-G

100088199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116420757-G-T

100088241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116420715-G-A

100088241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116420715-G-T

100102980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116415130-G-A

100103021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116415089-T-C

100103164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414947-T-C

100103198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414914-T-G

http://identifiers.org/hco/1/GRCh38#100103231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116414878-C-A

100103242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414864-T-G

100103253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414858-G-A

100103375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414718-T-A

100103417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414682-T-G

100106849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116413048-G-A

http://identifiers.org/hco/1/GRCh38#100106858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116413039-A-C

http://identifiers.org/hco/1/GRCh38#100106879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116413013-A-C

100106968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116412923-T-C

100106987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116412904-T-C

100107043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412855-A-G

100107072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412832-A-T

http://identifiers.org/hco/1/GRCh38#100107074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116412830-A-C

100107103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412812-T-C

100107116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412799-T-C

100107138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412777-T-C

100107387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116412537-A-G

100107394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116412530-G-T

http://identifiers.org/hco/1/GRCh38#100107540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116412384-A-C

100107540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116412384-A-G

100107719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 116412205-T-C

100107950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116411957-G-A

100108466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116410620-A-G

http://identifiers.org/hco/1/GRCh38#100108563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116410519-C-A

100108787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116410334-T-G

100109549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408373-A-G

100109681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408264-T-C

100109739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408217-T-A

100109824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408154-T-C

http://identifiers.org/hco/1/GRCh38#100110140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116407889-C-A

100110140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407889-C-G

100110175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407857-T-A

100110175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407857-T-C

100110233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407796-A-G

http://identifiers.org/hco/1/GRCh38#100110241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116407788-A-C

http://identifiers.org/hco/1/GRCh38#100110278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116407758-A-C

100110299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116407737-A-T

100110386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116407650-T-C

100110479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116407557-T-C

100110507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407537-A-G

100110507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407537-A-T

http://identifiers.org/hco/1/GRCh38#100110562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116407494-A-C

100110620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407457-T-G

100118867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404183-A-G

100118867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404183-A-T

100118908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404144-T-A

100118908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404144-T-C

100118908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404144-T-G

100119025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116404023-G-A

100119025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116404023-G-C

100119025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116404023-G-T

100119082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116403966-T-C

100119127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116403921-T-C

100119133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116403915-A-G

100119133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116403915-A-T

100119157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403891-A-G

100119178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403870-T-A

100119178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403870-T-C

100119181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403867-T-C

100119181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403867-T-G

100119182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403866-A-G

100119195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403854-G-A

100119195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403854-G-T

100119203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403846-T-C

http://identifiers.org/hco/1/GRCh38#100119218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116403832-A-C

100119220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403830-G-A

100119220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403830-G-T

http://identifiers.org/hco/1/GRCh38#100119251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116403802-C-A

100119251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403802-C-T

100119387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403711-T-A

100119447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403648-G-A

100120082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402611-G-A

100120317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402171-G-A

100120317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402171-G-T

100120362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402128-G-A

100120362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402128-G-T

http://identifiers.org/hco/1/GRCh38#100120383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116402107-A-C

100120383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402107-A-G

100120383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402107-A-T

100120462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116402028-A-G

100120503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401985-A-T

http://identifiers.org/hco/1/GRCh38#100120587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116401920-A-C

100121122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401388-C-T

100121338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401180-A-G

100121340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401178-T-C

100121457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116401062-G-A

100121457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116401062-G-T

100121502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116401017-G-A

100121502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116401017-G-T

100121517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116401002-A-G

100121589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400931-A-G

100121589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400931-A-T

http://identifiers.org/hco/1/GRCh38#100121600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116400920-C-A

100121600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400920-C-G

100121826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400709-C-G

http://identifiers.org/hco/1/GRCh38#100122230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116399548-A-C

http://identifiers.org/hco/1/GRCh38#100122233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116399545-C-A

100122300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399474-G-A

100122300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399474-G-T

100122358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399434-G-T

100122398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116399398-T-C

100122463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116399333-A-G

http://identifiers.org/hco/1/GRCh38#100122964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116399092-C-A

100122964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399092-C-T

100123014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399057-T-G

100123079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398999-G-A

100123079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398999-G-T

http://identifiers.org/hco/1/GRCh38#100123082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116398996-C-A

100123082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398996-C-G

100123127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398958-A-G

100123160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398937-T-C

100123252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116398881-A-T

100123323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398811-A-G

100123323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398811-A-T

http://identifiers.org/hco/1/GRCh38#100123373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116398780-C-A

100123374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398779-A-G

100123423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398734-T-C

100123439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398719-G-C

100123533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398644-G-T

http://identifiers.org/hco/1/GRCh38#100123595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116398594-C-A

100123690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398520-T-A

100123690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398520-T-C

100123870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 116398353-A-T

100123894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116398330-G-A

100124201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398081-C-T

100125806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397263-G-T

100125901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116397150-G-C

100125901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116397150-G-T

http://identifiers.org/hco/1/GRCh38#100125931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116397120-A-C

100125947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116397104-A-G

100125956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397095-C-T

100125984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397070-G-A

100125984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397070-G-T

100126035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397021-G-C

100126035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397021-G-T

100126039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397019-T-C

100126926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396049-T-C

100126928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396047-T-C

http://identifiers.org/hco/1/GRCh38#100127241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116395484-A-C

100127355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116395367-T-C

100127355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116395367-T-G

100128544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116394209-T-C

100129647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391961-G-A

100129649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391959-C-G

100129649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391959-C-T

100129703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391904-G-A

100129913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391703-T-A

100129958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391659-A-G

100130038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391574-C-T

100130171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391336-T-C

100130221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391289-G-A

100131333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390168-G-A

100131333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390168-G-T

100131757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389687-G-A

100131810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389618-A-G

100132320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389217-C-T

100132535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116389034-T-C

100132588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388976-G-C

100132608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388956-C-G

100132608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388956-C-T

100132663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388903-G-A

100132663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388903-G-T

100132691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116388875-T-C

100132731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388836-T-C

100132848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116388727-G-A

100132848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116388727-G-T

http://identifiers.org/hco/1/GRCh38#100132863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116388712-C-A

100132863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25403
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116388712-C-T