48170767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13012329-G-C

48170767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13012329-G-T

http://identifiers.org/hco/19/GRCh38#48170768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13012328-C-A

48170769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13012327-T-C

48170883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13012211-G-A

http://identifiers.org/hco/19/GRCh38#48171147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13011939-C-A

http://identifiers.org/hco/19/GRCh38#48171151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13011935-A-C

48171680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13011459-A-T

http://identifiers.org/hco/19/GRCh38#48171682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13011457-C-A

48171682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13011457-C-T

48171722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13011422-A-G

48171722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13011422-A-T

48171828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense variant
orthologous variants: 13011319-G-A

48171896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense variant
orthologous variants: 13011251-C-T

48171921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense variant
orthologous variants: 13011226-A-G

http://identifiers.org/hco/19/GRCh38#48171923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13011224-C-A

48171923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13011224-C-T

48172010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13011137-G-C

48172124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13011027-G-A

48172124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13011027-G-T

http://identifiers.org/hco/19/GRCh38#48172160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13011007-C-A

48172160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13011007-C-T

48172185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13010978-A-G

http://identifiers.org/hco/19/GRCh38#48174624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13009821-C-A

48174644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13009804-T-G

http://identifiers.org/hco/19/GRCh38#48174696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13009755-C-A

48174696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13009755-C-G

48174981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13009438-T-C

48175183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13009062-G-T

48175222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13009023-C-T

48175363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008893-C-T

48175403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008848-C-T

48175510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008780-G-A

48175624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008687-G-A

48175624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008687-G-C

48175624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008687-G-T

48175653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008659-G-C

48175728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008611-C-T

48175849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13008507-C-T

48176605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13007930-G-A

48176605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13007930-G-C

48176717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13007833-G-T

48176720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13007830-G-A

48177689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006882-G-A

48177777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006794-T-A

48177786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006784-C-G

48177793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006777-G-A

48177843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006739-G-A

48177954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006673-A-G

48178583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron variant
orthologous variants: 13006249-T-C

48181423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13004886-G-T

48181546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13004770-A-G

http://identifiers.org/hco/19/GRCh38#48181585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13004731-C-A

48182022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13004098-G-A

48182056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003964-T-A

48182118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003901-C-G

48182118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003901-C-T

48182121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003898-A-G

48182333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003698-G-A

48182411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003623-G-A

48182411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003623-G-T

48182723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13003303-C-G

48182785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003241-G-A

48182785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003241-G-T

48182801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003235-G-A

48182828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003207-G-A

48182828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003207-G-C

48182828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003207-G-T

48182841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003194-G-T

48182881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003184-T-C

48182881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003184-T-G

48183033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003069-C-T

http://identifiers.org/hco/19/GRCh38#48183038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13003064-C-A

48183038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003064-C-G

48183038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003064-C-T

48183086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003017-T-A

48183086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003017-T-C

48183086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13003017-T-G

http://identifiers.org/hco/19/GRCh38#48186513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13001258-C-A

48186513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13001258-C-T

48186655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13001137-A-G

48186707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13001085-G-A

http://identifiers.org/hco/19/GRCh38#48186739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13001053-C-A

48186739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13001053-C-G

48186739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13001053-C-T

48186776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13001029-A-G

48186811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13001003-A-G

http://identifiers.org/hco/19/GRCh38#48186816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13000998-C-A

http://identifiers.org/hco/19/GRCh38#48186892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13000922-C-A

http://identifiers.org/hco/19/GRCh38#48187191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#13000652-C-A

48187191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13000652-C-T

48187274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13000610-T-C

48187997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13000521-C-T

48188034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13000485-G-A

http://identifiers.org/hco/19/GRCh38#48192605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12998178-C-A

48192701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12998093-T-G

48193681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996514-G-A

48193874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996316-C-T

48193969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996221-G-A

48193973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996217-A-G

48193977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996213-A-T

48194009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996181-T-C

48194086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996111-G-T

48194158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12996049-T-C

48194427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12995807-G-C

48194532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995690-G-A

48194532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995690-G-C

48194532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995690-G-T

48194535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995687-G-A

48194535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995687-G-C

48194535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12995687-G-T

48194542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12995680-A-T

48194617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12995600-T-G

http://identifiers.org/hco/19/GRCh38#48194647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995570-C-A

48194647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12995570-C-T

48194665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995552-T-C

48194665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995552-T-G

48194702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995515-T-A

48194719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995498-A-G

48194719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995498-A-T

48194800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995417-G-A

http://identifiers.org/hco/19/GRCh38#48194803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995414-C-A

48194803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12995414-C-T

48194827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995390-G-A

48194849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995368-T-A

48194849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995368-T-C

http://identifiers.org/hco/19/GRCh38#48194905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995312-A-C

48194905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995312-A-G

48194905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995312-A-T

http://identifiers.org/hco/19/GRCh38#48194911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995306-C-A

48194911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995306-C-T

48195004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995213-G-A

48195004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995213-G-C

48195004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995213-G-T

http://identifiers.org/hco/19/GRCh38#48195016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995201-C-A

48195016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995201-C-G

48195016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995201-C-T

http://identifiers.org/hco/19/GRCh38#48195073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12995144-C-A

48195073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995144-C-T

48195151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995066-G-A

48195151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995066-G-C

48195178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12995039-G-A

48195409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994808-G-T

48195410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994807-G-A

48195410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994807-G-T

48195488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994729-G-A

48195530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994459-G-A

48195530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994459-G-T

48195589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 12994400-C-T

48195611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994690-G-A

48195611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994690-G-T

48195706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994604-A-G

48195747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12994563-G-A

48195747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12994563-G-C

48195747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12994563-G-T

48195885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12994524-C-G

48195885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12994524-C-T

48195950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994459-G-A

48195950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994459-G-T

http://identifiers.org/hco/19/GRCh38#48196009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12994400-C-A

48196009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994400-C-G

48196067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994348-T-C

48196144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994283-C-G

48196144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994283-C-T

48196229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994198-A-G

48196330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994100-G-A

48196330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994100-G-C

48196330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994100-G-T

48196337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994093-G-A

48196337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994093-G-T

48196360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994070-G-A

48196360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12994070-G-T

http://identifiers.org/hco/19/GRCh38#48196473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12993957-C-A

48196473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12993957-C-T

48196474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993956-A-G

48196612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993818-A-G

48196747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993683-G-A

48196747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993683-G-T

48196774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12993656-T-C

48196774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993656-T-G

48196819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12993611-G-A

48196920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993505-T-C

48196920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993505-T-G

48196924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993501-G-A

48196924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993501-G-T

48196942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993483-T-C

48197029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993400-G-A

48197029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993400-G-T

48197085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993336-A-G

48197085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993336-A-T

48197169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993247-T-A

48197169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993247-T-G

48197347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993134-G-A

48197347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993134-G-C

48197377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993103-G-A

48197386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993094-T-A

48197386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993094-T-C

48197386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993094-T-G

48197392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993088-G-A

48197392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993088-G-C

http://identifiers.org/hco/19/GRCh38#48197419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12993055-A-C

48197419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993055-A-G

48197441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12993043-A-G

http://identifiers.org/hco/19/GRCh38#48197552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#12992967-C-A

48197552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12992967-C-G

48197552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34495
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12992967-C-T