30881993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149314949-A-G

http://identifiers.org/hco/13/GRCh38#30882000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149314956-C-A

30882000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149314956-C-T

30882071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149315025-A-G

30882086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149315040-G-A

30882086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149315040-G-T

30882236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149315213-G-T

30882269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149315263-A-G

30882674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149315682-T-C

30882754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149315758-A-G

30882793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149315786-G-T

http://identifiers.org/hco/13/GRCh38#30882871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149315863-A-C

30883032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149316032-A-G

http://identifiers.org/hco/13/GRCh38#30883085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149316085-C-A

http://identifiers.org/hco/13/GRCh38#30886559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149318579-C-A

30886574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318593-T-C

30886574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318593-T-G

30886579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318598-G-A

30886615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318625-G-A

30886636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318646-T-C

30886764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318763-G-A

30886771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318772-G-C

30886775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318776-C-T

30886813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149318814-C-T

30888772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149321342-T-C

30889089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149321616-C-G

30889089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149321616-C-T

http://identifiers.org/hco/13/GRCh38#30891948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149326001-A-C

30892051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149326087-G-T

30892171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149326199-G-A

30892354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149326382-G-A

http://identifiers.org/hco/13/GRCh38#30892462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149326559-A-C

30892629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149326728-A-T

http://identifiers.org/hco/13/GRCh38#30892669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149326759-C-A

30892975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149327109-C-T

30893043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149327178-A-G

30893129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327263-G-T

30893192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327340-C-T

30893224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327400-G-A

30893224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327400-G-T

30893296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327483-G-A

30893341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149327582-G-A

30893379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149327623-T-G

30893527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149327968-G-T

30893665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149328118-G-A

http://identifiers.org/hco/13/GRCh38#30893667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149328120-C-A

30894425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149328785-A-G

30898730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149330020-G-A

30898807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149330087-C-T

30898808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149330088-G-A

30899148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149330406-C-T

30899196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149330453-T-C

http://identifiers.org/hco/13/GRCh38#30899319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149330579-C-A

30899319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149330579-C-T

30899430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149330689-A-G

30900789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331526-C-T

30900876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331611-G-C

30900905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331640-C-G

30900966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331701-C-T

30901060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331796-A-G

http://identifiers.org/hco/13/GRCh38#30901063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149331799-C-A

30901107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331829-C-T

30901111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331833-C-G

30901134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331853-G-T

30901140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331859-T-C

30901203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331904-A-G

30901237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331934-A-G

30901237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331934-A-T

30901240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149331937-T-C

http://identifiers.org/hco/13/GRCh38#30901293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149331986-A-C

30901339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149332031-G-A

30901359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149332055-C-T

http://identifiers.org/hco/13/GRCh38#30901565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149332234-A-C

30902037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149333811-T-C

30902326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149333890-T-C

http://identifiers.org/hco/13/GRCh38#30902333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149333897-A-C

30902441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149333993-A-G

30905780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149334826-G-A

30905853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149334903-C-T

30905854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149334904-T-C

30906054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335040-T-C

30906054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335040-T-G

30906057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335043-G-A

30906057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335043-G-C

30906057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335043-G-T

http://identifiers.org/hco/13/GRCh38#30906086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335071-A-C

30906086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335071-A-G

30906086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335071-A-T

30906145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335134-T-A

30906145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335134-T-C

30906262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335254-G-A

30906262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335254-G-C

30906262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335254-G-T

http://identifiers.org/hco/13/GRCh38#30906384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335357-C-A

30906384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335357-C-T

http://identifiers.org/hco/13/GRCh38#30906415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335377-C-A

30906415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335377-C-G

30906415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335377-C-T

30906431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335390-G-A

30906431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335390-G-T

30906432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335391-G-A

30906432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335391-G-C

30906432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335391-G-T

http://identifiers.org/hco/13/GRCh38#30906438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335397-C-A

30906438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335397-C-G

http://identifiers.org/hco/13/GRCh38#30906587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335514-C-A

30906587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335514-C-G

30906587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335514-C-T

30906596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335523-C-T

http://identifiers.org/hco/13/GRCh38#30906655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335582-C-A

30906655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335582-C-T

http://identifiers.org/hco/13/GRCh38#30906671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335598-C-A

30906671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335598-C-T

30906701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335628-G-A

30906701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335628-G-C

30906701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335628-G-T

http://identifiers.org/hco/13/GRCh38#30906712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335639-C-A

30906712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335639-C-T

30906716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335643-G-A

30906716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335643-G-C

30906716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335643-G-T

http://identifiers.org/hco/13/GRCh38#30906758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335685-C-A

30906758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149335685-C-T

http://identifiers.org/hco/13/GRCh38#30906820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149335747-C-A

30906820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335747-C-T

30906843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335758-G-A

30906843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335758-G-C

30906843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149335758-G-T

http://identifiers.org/hco/13/GRCh38#30907315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149336110-C-A

30907315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149336110-C-T

30907386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149336176-C-T

30907461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149336276-A-G

30907809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149336529-C-T

30908276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149337179-A-G

30908433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149337341-A-G

30908476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149337387-G-A

30908499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149337410-A-G

30909435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149338879-C-T

http://identifiers.org/hco/13/GRCh38#30909473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149338917-C-A

30909791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149339197-G-A

30909791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149339197-G-T

30910102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149339499-T-A

30910116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149339513-G-A

30910383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149340151-G-A

30910383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149340151-G-T

30910944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149340738-T-C

30911378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149341426-G-C

30911409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149341455-C-T

30911594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149341671-T-C

http://identifiers.org/hco/13/GRCh38#30911595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149341672-A-C

http://identifiers.org/hco/13/GRCh38#30914188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149343341-C-A

http://identifiers.org/hco/13/GRCh38#30914259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149343447-A-C

30914260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149343448-T-C

30916455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344075-C-T

30916489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344109-C-G

30916489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344109-C-T

30916490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344110-A-G

30916598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344215-G-A

30916639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344659-T-A

30916679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344699-A-G

30916768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149344785-A-T

http://identifiers.org/hco/13/GRCh38#30916777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149344794-C-A

30916777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 149344794-C-G

30916785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149344802-G-T

30916804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149344825-G-A

30916907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149344928-T-C

30916994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345015-C-T

30917047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345063-T-C

30917113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345328-T-A

30917113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345328-T-C

30917198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345403-T-C

30917330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345526-T-C

30917341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345537-T-C

http://identifiers.org/hco/13/GRCh38#30917344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149345540-C-A

30917344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149345540-C-T

http://identifiers.org/hco/13/GRCh38#30917475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149345671-C-A

30918963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149347314-G-A

30918997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 149347348-G-T

30919014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347362-A-G

30919092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347436-T-G

30919233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347549-A-G

http://identifiers.org/hco/13/GRCh38#30919239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149347555-A-C

30919263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347580-A-G

30919265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347582-A-T

30919427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347725-T-C

30919432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347730-C-T

30919598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149347904-A-G

http://identifiers.org/hco/13/GRCh38#30919619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149347927-C-A

30919690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348203-T-C

30919787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348292-A-G

30919789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348294-G-A

30919808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348310-T-A

30919876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348365-G-C

30919895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348384-A-G

30920391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348902-C-T

http://identifiers.org/hco/13/GRCh38#30920412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149348923-C-A

http://identifiers.org/hco/13/GRCh38#30920422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149348933-C-A

30920429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149348952-A-T

30920729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149349202-T-C

30920781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149349247-A-G

30921197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350557-T-A

30921197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350557-T-C

30921201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350561-G-T

30921217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350577-T-A

30921220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350580-G-T

30921476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350606-T-C

30921477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350607-G-A

30921477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350607-G-T

30921514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350642-G-T

30921515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149350643-G-T

http://identifiers.org/hco/13/GRCh38#30921531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149350659-A-C

http://identifiers.org/hco/13/GRCh38#30921547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149350672-C-A

30921788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149350913-T-A

30921788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149350913-T-C

30921894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149351018-G-A

30921900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149351024-G-A

30921900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149351024-G-C

30922578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149351830-G-T

30922721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149351943-T-C

30922850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149352055-T-C

30924189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149353137-G-T

http://identifiers.org/hco/13/GRCh38#30924196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353144-C-A

30924261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149353202-T-C

30924261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149353202-T-G

30924268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149353209-T-G

30924279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149353220-T-C

http://identifiers.org/hco/13/GRCh38#30924486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353423-C-A

30924486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353423-C-T

30924508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353445-G-A

30924508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353445-G-T

30924511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353448-G-A

http://identifiers.org/hco/13/GRCh38#30924638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353557-A-C

30924638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353557-A-G

http://identifiers.org/hco/13/GRCh38#30924639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353558-C-A

30924639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353558-C-G

30924639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353558-C-T

30924673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353591-A-T

30924735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353641-G-A

30924735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353641-G-T

http://identifiers.org/hco/13/GRCh38#30924740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353646-C-A

30924772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353671-T-A

30924772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353671-T-C

30924772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353671-T-G

30924781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353680-A-G

30924813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353720-G-A

30924813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353720-G-T

30924834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353742-G-T

30924868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353772-G-T

http://identifiers.org/hco/13/GRCh38#30924890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353789-A-C

http://identifiers.org/hco/13/GRCh38#30924892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353791-C-A

30924892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353791-C-T

30924902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353793-A-G

http://identifiers.org/hco/13/GRCh38#30924932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149353819-C-A

30924932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353819-C-G

30924986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353872-T-A

30925004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353882-A-G

30925005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353883-T-G

30925069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353932-G-A

30925142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149353977-A-T

30925189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354006-G-C

30925189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354006-G-T

30925199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354016-T-A

30925203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354020-T-A

30925209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354026-G-A

30925308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354138-G-A

30925322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354153-G-A

30925444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149354438-T-C

30925577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149354574-A-G

30925595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149354589-G-T

30925652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149354643-A-G

30925805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149354777-A-G

30926220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149355352-G-C

30926222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149355354-G-C

30928835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149357421-G-T

http://identifiers.org/hco/13/GRCh38#30928970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149357578-C-A

30929938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359516-C-T

30930004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359563-A-T

30930174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359705-C-T

30930282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359826-A-G

30930282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359826-A-T

30930377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359886-C-G

30930487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149359987-G-T

http://identifiers.org/hco/13/GRCh38#30930578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149360095-C-A

30930580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149360097-G-A

30930580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149360097-G-T

http://identifiers.org/hco/13/GRCh38#30930611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149360128-C-A

30930611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149360128-C-T

30930631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149360154-A-G

http://identifiers.org/hco/13/GRCh38#30930802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149360310-C-A

30930804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non coding transcript exon variant
orthologous variants: 149360312-T-C

30931116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149360641-G-C

http://identifiers.org/hco/13/GRCh38#30931219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149360760-C-A

http://identifiers.org/hco/13/GRCh38#30931387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149361030-A-C

30931423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non coding transcript exon variant
orthologous variants: 149361064-G-T

http://identifiers.org/hco/13/GRCh38#30931450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149361091-A-C

30931486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: non coding transcript exon variant
orthologous variants: 149361129-C-T

30932251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362409-T-C

30932314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362470-T-C

http://identifiers.org/hco/13/GRCh38#30932346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149362502-C-A

30932351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362507-G-A

30932351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362507-G-T

30932383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362542-T-C

http://identifiers.org/hco/13/GRCh38#30932392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149362551-A-C

30932392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149362551-A-G

30932581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149363059-G-A

http://identifiers.org/hco/13/GRCh38#30932734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149363210-A-C

30932734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363210-A-G

30932748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363224-C-G

http://identifiers.org/hco/13/GRCh38#30932803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149363279-C-A

30932803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363279-C-T

30932815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363292-G-T

http://identifiers.org/hco/13/GRCh38#30932826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149363303-C-A

30932826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363303-C-T

30932860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363350-A-G

http://identifiers.org/hco/13/GRCh38#30932884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149363373-C-A

30932884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363373-C-G

30932890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363379-A-T

30932930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363412-T-C

http://identifiers.org/hco/13/GRCh38#30932947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149363429-C-A

30932947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363429-C-G

30932947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363429-C-T

30933078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363541-C-T

30933134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363597-G-T

30933186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363652-G-A

30933274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363707-G-A

30933274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363707-G-T

30933417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363821-G-T

30933586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149363970-T-G

http://identifiers.org/hco/13/GRCh38#30933705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149364118-C-A

30933714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364127-G-T

30933742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364150-G-T

http://identifiers.org/hco/13/GRCh38#30933806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149364211-C-A

30933806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364211-C-G

30933806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364211-C-T

30933817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364222-A-G

30933817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364222-A-T

30933820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364225-G-C

http://identifiers.org/hco/13/GRCh38#30933838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#149364248-C-A

30933838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149364248-C-T