3357983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72302095-G-A

3358117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301878-G-A

3358183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301807-G-A

3358251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301740-T-C

3358263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301728-G-C

3358270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301721-C-T

3358283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301708-C-T

3358406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301584-C-T

3358472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301521-T-C

3358515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301479-C-T

3358627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72301348-A-T

3362940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293929-T-C

3363003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293867-T-A

3363008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293862-A-G

3363052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293819-T-C

3363330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293537-T-C

3363687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293217-T-G

3363745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293145-C-G

3363757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72293135-G-C

3364131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292671-T-A

3364337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292475-T-C

3364345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292467-T-C

3364451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292390-T-A

3364479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292368-G-A

3364511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292337-G-T

3364515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72292333-A-G

http://identifiers.org/hco/5/GRCh38#3365029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72291601-A-C

http://identifiers.org/hco/5/GRCh38#3365060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72291572-C-A

3365080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72291552-T-A

3365122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72291510-T-G

3365240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72291419-T-C

3365256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72291402-G-A

3365269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72291389-A-T

3375021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72289748-G-A

3375052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72289736-T-C

http://identifiers.org/hco/5/GRCh38#3375113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72289679-A-C

3375633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72289241-C-T

3375703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72289178-T-C

3375850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72289069-G-A

3375909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72288985-G-C

3375909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72288985-G-T

3375942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72288952-C-T

3380000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284684-C-T

3380046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284637-T-C

3380126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284558-T-C

3380290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284395-G-C

3380290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284395-G-T

3380584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284129-C-T

3380604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284105-C-G

3382385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72282638-G-A

3383418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72281748-A-T

3385851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72279317-T-C

3386156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72279023-C-T

3386957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277988-G-A

3386987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277958-T-G

3387049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277896-T-C

3387052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277893-T-A

3387140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277821-G-A

3387233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277723-T-G

http://identifiers.org/hco/5/GRCh38#3387439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72277525-C-A

3387534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277456-C-T

3387535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277455-T-C

http://identifiers.org/hco/5/GRCh38#3387724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72277279-C-A

3387724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277279-C-G

3387724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277279-C-T

3387760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277242-C-G

3387896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277127-T-C

3389626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72275840-A-G

3389626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72275840-A-T

3389691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72275758-G-A

3389760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72275689-A-G

3389776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72275667-T-C

http://identifiers.org/hco/5/GRCh38#3391811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72271723-A-C

3391825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72271709-G-A

3393230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72270995-G-A

3393230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72270995-G-C

3393258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72270974-G-C

3393491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72270756-C-T

3393849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72270410-G-A

3394466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72269817-A-T

3394606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72269673-T-C

3395429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268855-G-A

3395488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268818-A-G

3395491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268815-T-A

3395511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268795-G-C

3395511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268795-G-T

http://identifiers.org/hco/5/GRCh38#3395579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72268724-A-C

3395580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268723-C-T

3395633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268674-G-C

3395660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268647-A-G

3395902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72268335-C-T

3396589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267526-C-T

3396828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267329-G-A

3396884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267271-A-T

http://identifiers.org/hco/5/GRCh38#3397249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72266818-C-A

3397457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266595-C-T

3397640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266403-T-G

3397728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266361-G-A

3397900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266265-C-T

3397924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266255-C-T

3398082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266140-G-C

3398088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72266134-T-A

3398249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265996-A-T

3398609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265648-A-G

3398757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265515-C-T

3398881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265405-G-T

3399472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265184-G-A

3399535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72265121-T-C

http://identifiers.org/hco/5/GRCh38#3399825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72264904-A-C

3399923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264833-T-A

3399923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264833-T-G

3400041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264721-T-C

http://identifiers.org/hco/5/GRCh38#3400046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72264716-C-A

3400122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264645-G-A

3400154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264593-A-T

3400184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264565-G-A

3400184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264565-G-C

3400624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72264151-A-T

http://identifiers.org/hco/5/GRCh38#3400827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72263963-C-A

3400829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263961-G-A

http://identifiers.org/hco/5/GRCh38#3400906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72263924-C-A

3400906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263924-C-T

3400979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263825-C-G

3401169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263645-G-A

3401201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72263613-G-T

3413307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259024-T-C

3413658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258696-T-C

3413700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258655-A-G

3413773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258589-C-T

http://identifiers.org/hco/5/GRCh38#3413784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72258578-A-C

3413784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258578-A-G

3413809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72258556-A-T

3414803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257222-C-T

3414862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257153-C-G

3414862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257153-C-T

3415276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256747-T-C

3415352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256685-G-C

3415352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256685-G-T

3415359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256678-T-C

3415422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256620-T-C

3421825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253993-T-C

http://identifiers.org/hco/5/GRCh38#3421873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72253953-A-C

3421946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253883-A-G

3422166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253711-C-T

3422210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253645-T-C

3422224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253628-A-G

3422233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253619-T-C

http://identifiers.org/hco/5/GRCh38#3422259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72253599-C-A

3422272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253586-G-A

3422272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253586-G-T

http://identifiers.org/hco/5/GRCh38#3422297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72253567-C-A

3422297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253567-C-T

3422348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253520-C-T

3422455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253416-G-A

3422455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253416-G-C

3422455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253416-G-T

3422473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: non coding transcript exon variant
orthologous variants: 72253396-G-A

3422941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252779-T-C

3422942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252778-G-T

3423151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252427-C-G

3423219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252357-C-T

3423320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252248-C-T

3423346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72252227-A-T

3423930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251682-C-G

3424232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251167-C-T

3424765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250654-G-A

3425087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250334-A-G

3425201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250248-G-A

3425256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250194-T-C

3425296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250159-C-G

http://identifiers.org/hco/5/GRCh38#3425399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72250033-A-C

3425451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249975-C-T

3425463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249963-C-T

3425464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249962-A-G

http://identifiers.org/hco/5/GRCh38#3426145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72249667-C-A

3426145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249667-C-G

3426399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249418-T-C

3426427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249392-G-A

3426646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247298-G-T

3426657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247287-T-C

3426940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247009-G-T

3427173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72246787-A-G

3427263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72246705-G-A

3428571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72245487-G-A

3429224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244875-T-G

3429250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244855-C-T

3429260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244845-C-T

3429263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244842-T-C

3429475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72244645-G-A

3430620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242627-C-T

3430787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242460-T-C

3430974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242255-G-A

3431023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72242214-T-C

3431283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241965-G-T

3431357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241890-C-T

3431694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241715-A-G

3431920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241619-C-G

3431943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241596-T-C

3432136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241419-T-C

3432959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240729-T-C

3432971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240717-T-A

3433771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239886-G-A

3433873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239786-T-C

3433918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239742-A-G

3433991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239677-C-T

3434002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239666-G-A

3437083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238507-G-A

3437083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238507-G-T

3437223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238392-T-C

3437421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238242-T-C

3437447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238215-T-A

http://identifiers.org/hco/5/GRCh38#3437719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72237996-A-C

3437723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237992-C-T

3437771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237951-G-C

3437990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237785-A-G

3438015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237760-G-A

3438015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237760-G-C

3438037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237740-T-C

3438037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237740-T-G

3438112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237665-G-C

3438164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237599-G-A

3438202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237554-C-T

3438260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237499-G-T

3438346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237478-C-G

3438347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237477-T-C

3438366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237460-C-T

3438510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237337-C-T

3438520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237327-T-C

3438531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72237320-A-G

3452658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231080-C-T

3452664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231074-T-C

3452772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230975-G-C

3452772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230975-G-T

3452801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230951-A-G

3452801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230951-A-T

3452831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72230921-T-G

http://identifiers.org/hco/5/GRCh38#3452908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72230844-C-A

3452908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72230844-C-T

3452978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230774-T-C

http://identifiers.org/hco/5/GRCh38#3453058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72230695-C-A

http://identifiers.org/hco/5/GRCh38#3453065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72230687-C-A

3453095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230657-G-A

http://identifiers.org/hco/5/GRCh38#3453220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72230537-C-A

3453265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230517-T-A

3453322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230459-G-A

3453336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230445-T-C

3453425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230360-C-G

3453557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72230240-T-C

3454534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228063-G-C

3454721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227885-T-C

3454811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227800-C-G

http://identifiers.org/hco/5/GRCh38#3454876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72227735-A-C

3455273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227443-A-G

3455405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227315-T-G

3455417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227303-C-T

3455607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227110-T-G

3455630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227085-A-T

3456208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226530-C-G

3456237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226499-T-C

http://identifiers.org/hco/5/GRCh38#3456351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72226330-C-A

http://identifiers.org/hco/5/GRCh38#3456747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72226005-A-C

3457038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225776-G-A

3457607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225062-G-A

3457937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224721-A-G

3458084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224605-C-T

3458197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224515-C-G

http://identifiers.org/hco/5/GRCh38#3458198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72224514-C-A

3458223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224495-A-G

3458284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224441-G-C

3458305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224419-A-G

http://identifiers.org/hco/5/GRCh38#3458543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72224254-C-A

3458543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224254-C-G

3458543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224254-C-T

http://identifiers.org/hco/5/GRCh38#3459035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72223780-A-C

http://identifiers.org/hco/5/GRCh38#3459791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72222174-C-A

3462898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220811-C-T

3463006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220724-C-T

3463008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220722-G-T

3463141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220605-C-T

3463446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220304-G-A

3463461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220289-G-C

3463503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220253-A-G

3463641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220131-G-A

http://identifiers.org/hco/5/GRCh38#3463660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72220114-C-A

3463693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220081-T-A

3463727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220048-C-T

3463911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219851-A-G

3463970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219793-T-C

3464032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219732-A-G

http://identifiers.org/hco/5/GRCh38#3464043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72219721-A-C

3464229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219630-T-C

http://identifiers.org/hco/5/GRCh38#3464243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72219616-C-A

3464243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219616-C-T

3489305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211794-T-C

3489329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211768-C-G

3489329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211768-C-T

3489469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211624-G-A

3489469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211624-G-T

3489487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211606-G-A

3489487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211606-G-C

3489735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211359-G-A

3489735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211359-G-C

3489834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211257-T-C

http://identifiers.org/hco/5/GRCh38#3489869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72211222-A-C

3489902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211166-C-T

3489963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72211112-G-A

3490285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210840-G-A

3490285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210840-G-C

3490368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210747-A-G

3490514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210533-G-A

3490725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210347-C-T

3490773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210315-T-A

3490900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72210184-A-T

3491248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209835-C-T

3491283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209799-G-A

3491295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209787-G-A

http://identifiers.org/hco/5/GRCh38#3491569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72209546-C-A

3491569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209546-C-T

3491571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209544-T-A

3491571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209544-T-C

3491596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209500-C-G

3491665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209425-A-G

3491890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209218-C-T

3491953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72209156-C-T

3504860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72194178-T-C

3505054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193995-C-T

3505087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193963-A-G

3505302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193787-G-A

3505372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193747-T-C

3505399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193720-A-G

3505857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193330-G-C

3505905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193284-T-C

3505914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193275-T-C

3506036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193160-C-T

3506056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193151-G-A

3506480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192356-G-A

3506644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192192-A-T

3506710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192130-C-G

3506794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192034-A-G

3506836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192007-G-T

3507442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191484-T-C

3507527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191403-A-T

3507554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191376-C-T

3507730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191207-C-G

3507825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191117-C-T

3507834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191108-T-A

3507887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191062-T-C

3507942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183580-T-C

3508011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183497-A-G

3508033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183475-A-G

3508121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183396-A-G

3508135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183382-C-T

3508415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183107-G-A

3509451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180353-G-T

3509958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179826-G-A

3510110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179663-G-A

3510110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179663-G-C

http://identifiers.org/hco/5/GRCh38#3510661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72179154-A-C

3510718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179093-G-A

3510798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178998-G-T

3510816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178984-A-G

3510901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178903-C-T

3511136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178677-G-A

3511163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178654-T-C

3511375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178486-T-C

3511375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178486-T-G

3511388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178474-T-G

3511887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177992-T-C

3511892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177987-G-A

3511970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177919-G-A

3512016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177873-G-A

3512016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177873-G-T

3512088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72177801-A-G

3513260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72176609-A-G

3514120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175757-G-A

3514256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175628-G-C

3514256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175628-G-T

3514257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175627-C-T

3514303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175523-T-C

3514351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175471-G-T

3514502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175332-C-G

3514730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72175113-A-G

3515526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72174232-T-A

3515601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72174156-T-C

3515658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72174105-G-A

3515692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72174071-C-T

3515723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72174030-A-G

3516694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72173356-G-A

3516831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72173234-G-T

3517213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172884-A-T

3517302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172810-T-C

3517366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172750-G-A

3517470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172669-C-T

3517645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172505-C-T

3517744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172428-G-A

3517769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172409-T-G

3517812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172372-G-A

3517987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172209-T-C

3518100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72172105-T-A

3518342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171880-G-A

3518471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171752-C-T

3518520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171698-A-G

3518553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171662-A-G

3518559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171656-G-C

3518713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171533-T-A

3518809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171452-G-C

3518924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171356-G-T

3519290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171071-T-A

3519290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171071-T-C

3519290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171071-T-G

3519359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72171001-G-T

3519455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72170939-A-G

http://identifiers.org/hco/5/GRCh38#3525721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#72166360-A-C

3525721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72166360-A-G

3526080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72166042-C-T

3526161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165962-G-A

3526226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165897-G-C

3528763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165248-A-T

3528870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165134-A-G

3530476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164419-T-G

3530540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164359-A-G

3530543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164356-T-C

3531261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163646-A-G

3531567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72163333-T-A

http://identifiers.org/hco/5/GRCh38#3531659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#72163234-C-A

3531888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162979-A-G

3531958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162894-T-C

3531990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162860-G-A

3531990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162860-G-T

3532018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162847-A-G

3532225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162745-T-C

3532289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162687-C-T

3532352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162622-G-A

3532355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162619-T-C

3532405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162577-C-G

3532416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162560-C-T

3532421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162555-A-T

3532544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162455-C-T

3532559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162440-T-C

3532619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162391-G-C

3533013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162012-T-C

3533115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72161918-A-T