55866019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28877557-A-T

55866131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28877365-T-C

55866194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28877236-G-T

55866196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28877225-G-A

55866196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28877225-G-T

55866387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876928-T-C

55866502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876842-A-G

55866621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876722-T-C

55866865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876502-G-T

55866886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876481-A-G

55866941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876427-T-G

55867307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876084-A-G

55867307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876084-A-T

55867352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876045-G-A

55867373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876027-T-A

55867373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28876027-T-C

55868682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28873132-G-A

http://identifiers.org/hco/2/GRCh38#55868859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28873003-C-A

55868859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28873003-C-G

55869021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28872780-A-G

http://identifiers.org/hco/2/GRCh38#55869041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28872644-C-A

55869103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28872585-A-G

55870388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28872050-G-A

55870490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28871951-T-C

55870633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28871862-G-T

55870667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28871855-A-G

55870667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28871855-A-T

55870780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 28871744-G-A

55870788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28871736-T-C

55870862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28871662-A-G

http://identifiers.org/hco/2/GRCh38#55870920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28871604-A-C

http://identifiers.org/hco/2/GRCh38#55871395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28870993-C-A

55871440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870933-A-T

55871468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870902-T-C

55871552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870826-C-G

55871586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870795-G-A

55871597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870784-G-A

55871842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870473-T-C

55872187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28870145-C-T

55872387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28869923-T-C

55873448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28868492-G-A

55874117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28867880-T-C

http://identifiers.org/hco/2/GRCh38#55874235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28867763-A-C

55874681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28867219-T-G

55874922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28866988-A-G

55874961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28866952-T-C

55874993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28866920-C-T

55875062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 28866851-A-G

55875083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28866830-A-G

55875748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28866477-C-T

http://identifiers.org/hco/2/GRCh38#55876112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28866106-A-C

55876305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28866023-T-C

55876309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28866019-G-A

55876363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865976-A-G

55876551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865846-T-C

55876766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865635-A-G

55876938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865494-A-G

55877326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28865112-G-A

55877347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28865087-C-T

55877387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865061-A-T

55877411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28865037-G-A

http://identifiers.org/hco/2/GRCh38#55877436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28865012-C-A

55877669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28864780-A-G

55877729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864722-G-A

55877733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864718-T-G

55877873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 28864553-A-G

http://identifiers.org/hco/2/GRCh38#55877980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28864207-C-A

55877980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864207-C-T

55877995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864191-T-A

55878004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864182-T-A

55878004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28864182-T-C

http://identifiers.org/hco/2/GRCh38#55878497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28863726-C-A

http://identifiers.org/hco/2/GRCh38#55878558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28863668-A-C

55878779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28863481-A-G

http://identifiers.org/hco/2/GRCh38#55878946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28863317-A-C

55879698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28862776-A-G

55880485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861988-C-T

55880723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861762-C-G

55881099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861242-C-G

55881113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861215-T-G

55881208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861130-T-C

55881242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28861091-A-G

55881683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28860659-C-T

http://identifiers.org/hco/2/GRCh38#55881850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28860485-C-A

55882455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28859962-A-T

http://identifiers.org/hco/2/GRCh38#55883233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28859428-A-C

55883396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28859276-A-G

55883657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28859019-C-T

55883675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28859001-C-T

55883677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28858999-G-A

55883739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28858944-G-A

55883982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28858704-A-G

55884035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28858649-G-A

http://identifiers.org/hco/2/GRCh38#55884135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28858574-C-A

55885152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28857180-G-T

55885163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28857170-T-C

55885236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28857109-A-G

55885458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28856899-A-T

55885617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28856708-C-G

55885724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28856624-T-C

55885733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28856615-G-A

55885760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28856589-T-A

http://identifiers.org/hco/2/GRCh38#55885909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28856448-C-A

http://identifiers.org/hco/2/GRCh38#55886875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28856057-A-C

55886902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28856030-G-A

55886902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28856030-G-C

55886945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28855993-G-T

55886988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28855958-G-C

55887046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28855295-A-G

55887130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28855223-A-G

55887406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28854941-T-C

http://identifiers.org/hco/2/GRCh38#55887657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28854700-C-A

55887657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28854700-C-T

http://identifiers.org/hco/2/GRCh38#55887744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28854617-A-C

55887744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28854617-A-G

55888074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28854318-A-G

55888310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28854090-A-T

55888772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28853932-G-A

55889469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28853296-T-C

http://identifiers.org/hco/2/GRCh38#55889697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28852410-A-C

55889826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28852260-A-T

55889861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28852212-G-A

55889874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28852199-T-A

55889965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28852090-T-C

55890027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851984-A-G

55890029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851966-A-G

55890122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851882-A-T

55890397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851708-T-A

55890474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851630-A-T

http://identifiers.org/hco/2/GRCh38#55890503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28851601-C-A

http://identifiers.org/hco/2/GRCh38#55890660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28851402-C-A

http://identifiers.org/hco/2/GRCh38#55891123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28851152-A-C

55891123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28851152-A-G

55891566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850720-T-C

55891650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850651-A-G

55891650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850651-A-T

55891751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850563-G-A

55891857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850459-A-G

55891958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850395-T-C

55892097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850271-A-G

55892353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28850039-T-C

55892389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28849994-G-A

55892408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28849975-T-G

http://identifiers.org/hco/2/GRCh38#55892556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28849829-A-C

55893074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28849346-G-A

http://identifiers.org/hco/2/GRCh38#55893079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28849341-A-C

55893404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28849078-C-T

55893406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28849076-C-G

55893900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28848294-C-T

55894006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28848191-A-G

55894115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28848130-C-T

55894117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28848128-T-C

http://identifiers.org/hco/2/GRCh38#55894437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28847822-C-A

55894437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28847822-C-G

55894639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28847654-A-G

55896569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28847590-G-C

55897345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28846879-G-T

55898195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28845598-A-G

http://identifiers.org/hco/2/GRCh38#55898218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28845575-C-A

55898218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28845575-C-T

55898410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28845418-A-T

55898794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28845086-G-C

55899234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28844850-G-T

55899268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28844821-G-A

55899622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843708-T-A

55899622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843708-T-C

55899635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843694-G-C

55899651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843678-T-C

55899718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843615-G-A

55899842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843504-G-C

55899853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843492-A-G

55899979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843288-A-G

55900220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28843048-T-A

http://identifiers.org/hco/2/GRCh38#55900322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28842980-A-C

55901240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28842103-G-T

55901407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28841938-A-G

55901425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28841920-T-A

55901579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28841386-G-A

55901652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28841311-A-G

55901812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840979-G-C

55901875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840923-C-G

55901875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840923-C-T

55901987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840814-C-G

55902313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840540-A-G

http://identifiers.org/hco/2/GRCh38#55902356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28840500-C-A

55902478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840377-T-G

55902676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28840187-G-A

55902881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28839975-T-C

55903435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28839509-A-G

55903574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28839375-T-G

55904230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28839198-T-G

55904507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838942-A-T

55904512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838937-G-A

55904686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838753-G-T

55904925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838593-T-A

55904926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838592-G-T

http://identifiers.org/hco/2/GRCh38#55904952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28838568-C-A

55904952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838568-C-T

55904953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838567-T-A

55905119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838467-C-G

55905119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838467-C-T

http://identifiers.org/hco/2/GRCh38#55905191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28838389-C-A

55905191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838389-C-T

55905229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838344-G-T

55905246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838303-T-C

55905271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838271-A-G

55905430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28838163-A-G

55905934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837913-C-T

55905994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837841-T-C

55906054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837775-A-G

55906098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

55906111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

55906182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

55906182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-C

55906606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837535-A-G

http://identifiers.org/hco/2/GRCh38#55906614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28837527-A-C

55906700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837440-G-A

55906753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837400-G-A

55906818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837333-T-C

55906903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837292-G-A

55906904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837291-A-G

55906949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837253-A-T

55906959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28837245-C-T

http://identifiers.org/hco/2/GRCh38#55907342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28836919-A-C

55907889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28836516-C-T

55907966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28836437-C-T

55908395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28836001-C-T

55909267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28833389-A-G

55909309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28833355-G-A

55909517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28833178-A-G

55909564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28833132-G-A

55909600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28833110-A-G

55909848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28832577-A-G

55909895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28832497-C-T

55909923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28832469-G-A

55909988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28832414-A-G

http://identifiers.org/hco/2/GRCh38#55910014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28832389-C-A

55910786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28831669-T-C

55910916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28831552-T-C

55910917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28831551-G-A

55910984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28831480-G-A

55911085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28831400-A-G

55911859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28830806-T-C

55911878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28830789-T-C

55912043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28830627-T-A

55912048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28830622-A-G

55912395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28830345-T-C

55913455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28829800-C-T

55913572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28829691-A-G

55914261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28829366-C-T

55914818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28828891-G-A

55914914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28828795-A-G

55915192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28828521-C-T

http://identifiers.org/hco/2/GRCh38#55915487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28819784-A-C

55915586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28819692-G-A

55915586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28819692-G-T

55916468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28819149-A-G

55916826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28818857-T-A

55917050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28818640-G-T

55917158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28818531-T-C

http://identifiers.org/hco/2/GRCh38#55917186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28818503-A-C

55917370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28818311-G-C

55917600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28818074-C-T

55918157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28817575-A-G

55920229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28806584-A-G

55920927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805963-G-A

55920927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805963-G-C

55920927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805963-G-T

55921027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805884-G-A

55921027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805884-G-T

http://identifiers.org/hco/2/GRCh38#55921218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28805611-C-A

55921489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805370-T-C

55921651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805214-G-C

55921814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28805051-C-G

http://identifiers.org/hco/2/GRCh38#55921832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28805031-C-A

http://identifiers.org/hco/2/GRCh38#55921909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804985-C-A

55921909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28804985-C-T

55921940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28804965-G-A

55921979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804929-T-A

55921980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804928-G-T

55922051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804864-A-G

http://identifiers.org/hco/2/GRCh38#55922076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804839-C-A

http://identifiers.org/hco/2/GRCh38#55922155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804763-C-A

http://identifiers.org/hco/2/GRCh38#55922198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804709-C-A

55922198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804709-C-T

55922213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804694-C-T

55922258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804650-C-T

55922268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804640-T-C

http://identifiers.org/hco/2/GRCh38#55922329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804582-C-A

55922329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804582-C-T

http://identifiers.org/hco/2/GRCh38#55922451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804461-A-C

http://identifiers.org/hco/2/GRCh38#55922564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804358-A-C

55922564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28804358-A-G

http://identifiers.org/hco/2/GRCh38#55922567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804355-C-A

http://identifiers.org/hco/2/GRCh38#55922570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804352-C-A

55922570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 28804352-C-T

55922571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28804351-T-C

http://identifiers.org/hco/2/GRCh38#55922588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804334-A-C

55922588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804334-A-T

http://identifiers.org/hco/2/GRCh38#55922637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28804313-C-A

55922637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804313-C-T

55922784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804179-T-C

55922843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804146-G-A

55922843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804146-G-C

55922843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804146-G-T

55922919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28804072-T-G

http://identifiers.org/hco/2/GRCh38#55923029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28803948-C-A

55923038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28803938-T-C

55923057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28803915-T-C

55923331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28803664-A-G

55923449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28803553-T-C

55923595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28803416-G-A

55923595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28803416-G-T

55923674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28803362-G-A

55923674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28803362-G-T

55923712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 28803321-T-C

55923712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 28803321-T-G

55923713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 28803320-G-T

http://identifiers.org/hco/2/GRCh38#55923737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28803294-C-A

55923737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28803294-C-T

55923906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28803136-G-A

55923906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28803136-G-C

55923906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28803136-G-T

http://identifiers.org/hco/2/GRCh38#55923929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28803113-A-C

55924078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28802992-T-C

55924078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3218
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28802992-T-G