http://identifiers.org/hco/17/GRCh38#6057816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71628016-C-A

6057816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: non coding transcript exon variant
orthologous variants: 71628016-C-T

6057850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: non coding transcript exon variant
orthologous variants: 71628050-G-A

6057937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: non coding transcript exon variant
orthologous variants: 71628144-G-T

http://identifiers.org/hco/17/GRCh38#6058909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71628752-A-C

6059173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71629034-G-A

6059173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71629034-G-T

6059372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71629304-C-T

6059423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71629353-G-A

6059957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71629886-G-A

6060165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71630310-A-T

6060215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71630360-C-G

6060413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71630549-C-G

http://identifiers.org/hco/17/GRCh38#6060731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71630869-A-C

6060731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71630869-A-G

6061203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71631108-A-G

6061427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71631221-G-A

6061468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71631261-C-T

6061647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71631451-G-T

6061700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71631504-G-A

6061729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71631657-A-T

http://identifiers.org/hco/17/GRCh38#6063023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71634132-C-A

6063299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634457-G-T

6063523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634673-G-A

6063985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634836-G-T

6063996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634847-G-T

6064019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634867-G-A

6064101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634932-C-T

6064887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636737-C-G

6064964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636816-A-T

6065293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637130-G-T

6065412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637248-G-T

6065485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637323-T-C

6065518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637359-C-G

http://identifiers.org/hco/17/GRCh38#6065570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71637409-C-A

6065570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637409-C-T

6067502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638843-G-A

6067628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639033-G-A

6067700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639103-G-A

6067808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639219-G-C

6067849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639291-A-G

6067861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639303-C-T

6068485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639915-A-G

6068579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640052-G-A

6068590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640063-T-C

6068590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640063-T-G

http://identifiers.org/hco/17/GRCh38#6068681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71640390-C-A

6068681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640390-C-G

6068681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640390-C-T

http://identifiers.org/hco/17/GRCh38#6068881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71640531-C-A

6068953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640575-T-A

http://identifiers.org/hco/17/GRCh38#6068970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#71640592-C-A

6068970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640592-C-T

6068978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640600-G-A

6068978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640600-G-T

6069006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640624-C-G

6069007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640625-T-C

6069038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640654-T-A

6069038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640654-T-C

6069203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640831-T-C

http://identifiers.org/hco/17/GRCh38#6069264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#71640892-C-A

6069264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 71640892-C-T

6069395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640993-G-A

6069419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641017-G-A

6069419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641017-G-T

6069741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641247-G-A

6069782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641292-T-C

6069793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641303-G-T

6070266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641693-G-A

http://identifiers.org/hco/17/GRCh38#6070387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71641821-C-A

6070387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71641821-C-T

6070635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642038-G-A

6070635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642038-G-T

http://identifiers.org/hco/17/GRCh38#6070636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71642039-C-A

6070636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642039-C-T

6070693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642098-G-A

6070693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642098-G-C

6070693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642098-G-T

6070998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642363-T-C

http://identifiers.org/hco/17/GRCh38#6071047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71642412-C-A

6071047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642412-C-T

http://identifiers.org/hco/17/GRCh38#6071094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71642463-C-A

6071099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71642468-G-C

6071220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642591-G-A

http://identifiers.org/hco/17/GRCh38#6071305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71642672-C-A

6071305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642672-C-T

6071453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642820-C-G

6071494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71642864-C-T

6072081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71643408-A-G

6072285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71643605-G-T

6072489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71643805-C-T

http://identifiers.org/hco/17/GRCh38#6072928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71644211-C-A

6073029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644273-G-A

6073094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644337-A-T

6073132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644372-G-A

6073255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644493-G-T

6073268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644506-C-T

6073271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644509-C-T

6073315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644552-A-G

6073315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644552-A-T

6074774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646133-G-A

6074866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646291-T-G

6074909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646336-G-C

http://identifiers.org/hco/17/GRCh38#6074986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71646392-C-A

6075157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646564-C-T

6075568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646850-G-A

6075581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71646864-G-C

6075936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647171-A-T

6075943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647178-T-C

6076235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647420-T-C

6076242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647427-C-T

6076449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647618-G-T

http://identifiers.org/hco/17/GRCh38#6077819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71648083-C-A

http://identifiers.org/hco/17/GRCh38#6077953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71648205-C-A

6078143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648387-G-A

6078185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648496-C-G

6078185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648496-C-T

http://identifiers.org/hco/17/GRCh38#6078221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71648549-C-A

6078729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648991-G-C

6078779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649047-A-G

6078793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649062-A-G

6078911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649176-G-A

6078973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649239-G-A

6078973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649239-G-C

6078973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649239-G-T

6079077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649306-G-A

6079114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649341-A-G

6079151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649385-C-G

6079158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649392-G-A

6079295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649520-T-C

6079432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649653-C-T

6079734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649797-T-C

6079799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649865-G-T

6079850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649916-G-A

http://identifiers.org/hco/17/GRCh38#6080060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71650103-C-A

6080060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650103-C-T

6080107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650146-G-A

6080107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650146-G-T

http://identifiers.org/hco/17/GRCh38#6080252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71650287-C-A

6080252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71650287-C-T

6080277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71650313-A-G

6080286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71650322-G-A

6080286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71650322-G-T

6080343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650375-A-G

6080343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650375-A-T

6080356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650388-T-G

6080388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650418-T-C

6080388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650418-T-G

http://identifiers.org/hco/17/GRCh38#6080462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71650491-C-A

6080462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650491-C-T

6080476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650505-T-A

6080481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650510-G-T

6080546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71650562-G-T

6080715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71650731-G-A

6080715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71650731-G-C

http://identifiers.org/hco/17/GRCh38#6080809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71650825-C-A

6080809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 71650825-C-T

6080835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71650851-C-T

6080907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71650923-G-A

6080907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71650923-G-T

6080922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71650938-G-A

6080922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71650938-G-T

http://identifiers.org/hco/17/GRCh38#6081045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651052-C-A

http://identifiers.org/hco/17/GRCh38#6081081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651088-C-A

6081081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71651088-C-T

http://identifiers.org/hco/17/GRCh38#6081186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651159-C-A

6081186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651159-C-G

6081186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651159-C-T

6081216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651170-G-A

6081216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651170-G-T

http://identifiers.org/hco/17/GRCh38#6081218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651172-A-C

6081218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651172-A-G

6081415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651341-A-T

6081983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651705-C-T

6081986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651708-G-A

http://identifiers.org/hco/17/GRCh38#6081999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651721-A-C

6081999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651721-A-G

http://identifiers.org/hco/17/GRCh38#6082041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71651754-C-A

6082084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651801-G-T

6082186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71651897-A-G

6082415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652105-G-T

6082436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652123-C-G

6082489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652167-T-C

6082515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652192-G-A

6082626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652303-C-G

6082662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652337-C-T

6082702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652392-T-C

http://identifiers.org/hco/17/GRCh38#6082740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71652652-C-A

6082908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652923-T-A

6082963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71652978-G-T

6083017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71653035-G-C

6083109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71653112-A-T

http://identifiers.org/hco/17/GRCh38#6083143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71653146-A-C

6083374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71653412-G-A

6083404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71653441-A-G

6084340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71654046-A-G

6084386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71654087-A-G

6084393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71654093-C-G

6084829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71654528-G-A

6084844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71654543-C-T

http://identifiers.org/hco/17/GRCh38#6084881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71654580-C-A

6084979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71654697-G-A

6084979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71654697-G-T

6085231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71654947-C-T

6085467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655184-G-A

6085529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655246-T-C

6085851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655498-G-A

6085851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655498-G-T

6086057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655694-A-G

6086095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655729-T-G

6086099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71655733-G-T

6087005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656533-C-T

6087064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656577-C-G

6087078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656591-C-T

6087173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656691-C-T

6087249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656753-G-T

http://identifiers.org/hco/17/GRCh38#6087496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71656978-C-A

6087496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71656978-C-T

6087604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657083-A-G

6087840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657426-T-A

6087840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657426-T-C

6087900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657481-G-A

6087900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657481-G-T

6087941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657551-G-A

6087955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657581-G-A

6087955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657581-G-T

6088078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 71657703-C-T

6088127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657749-G-A

6088187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657808-C-T

6088193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71657814-G-T

http://identifiers.org/hco/17/GRCh38#6088208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71657829-A-C

6088702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658198-A-G

6089108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658365-T-C

6089124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658370-G-A

6089131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658377-A-G

6089303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658542-A-G

6089313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658550-C-T

6089333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658576-G-A

6089510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658707-G-A

6089624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658788-T-C

6089694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71658847-G-A

http://identifiers.org/hco/17/GRCh38#6090236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71659369-A-C

6090236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659369-A-T

6090238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659371-A-G

6090238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659371-A-T

6090330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 71659464-C-T

6090372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 71659506-C-G

6090372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 71659506-C-T

6090405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71659539-G-A

6090573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659691-C-T

6090598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659695-G-A

6090598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659695-G-T

http://identifiers.org/hco/17/GRCh38#6090648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71659734-C-A

6090648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659734-C-G

6090648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71659734-C-T

6092287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71660231-A-G

6092330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71660266-G-A

6092338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71660272-G-A

6092338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71660272-G-T

http://identifiers.org/hco/17/GRCh38#6092385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71660312-A-C

http://identifiers.org/hco/17/GRCh38#6093098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71660981-C-A

6093098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71660981-C-T

6093129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661013-G-C

6093163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661049-G-C

6093189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661077-G-A

6093403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661289-C-G

6093453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661346-T-A

6093524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661429-A-G

6093534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661439-C-T

6093920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661770-G-A

6094099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71661981-A-G

6094374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662234-A-G

6094955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662552-T-C

6094955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662552-T-G

http://identifiers.org/hco/17/GRCh38#6095056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71662639-C-A

6095066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662643-C-T

6095068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662645-A-G

6095357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662941-T-C

6095357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662941-T-G

6095366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662951-G-A

6095366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662951-G-T

6095374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662959-G-A

6095374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71662959-G-T

6095431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663009-G-T

6095501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663075-A-G

6095556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663130-T-A

6095648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663206-G-A

6095648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663206-G-T

6095689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663250-G-A

6095689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663250-G-T

6095798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663359-G-A

6095801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663362-A-G

6095801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663362-A-T

6095907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663458-G-A

6095920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663471-A-G

6095920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663471-A-T

6096249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663626-G-A

6096269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663642-C-T

6096448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663747-G-A

6096722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71663969-G-A

6097187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664296-G-A

6097187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664296-G-C

6097392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664502-C-T

6097462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664578-C-T

6097763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664929-T-C

6097824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71664990-G-T

6098467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71665270-C-G

6098848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71665692-G-A

6098855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71665699-T-C

6100112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71666077-A-T

6100234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71666138-A-G

6100340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71666228-A-G

6100976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71666650-T-C

6101063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71666715-T-A

6101417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71667010-G-A

6101463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71667053-T-C

6101714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71667805-T-C

6101796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 71667880-G-A

6102952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71669514-G-A

6103226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71669736-T-C

6103296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71669805-A-G

6103352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71669856-A-G

6103352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71669856-A-T

6103687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71670128-C-G

6105702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71670903-C-T

6105776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71670981-C-T

6105901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671089-G-A

6105901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671089-G-T

6106187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671330-G-A

6106362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671487-A-G

6106417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671541-G-A

6106540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671663-A-G

6106788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71671890-T-A

6106990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672064-T-C

6107009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672083-A-G

6107051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672134-G-A

6107135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672207-C-T

6107181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672244-G-A

6107212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672276-C-G

6107212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672276-C-T

6108085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672722-G-C

6108201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672811-T-C

6108206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672816-G-C

6108318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71672924-G-T

6108453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673037-G-T

6108537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673152-C-T

6108568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673183-G-A

6108957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673549-C-T

6108997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673585-C-T

6109006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673591-G-A

6109006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673591-G-C

6109324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673851-A-T

6109372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673905-C-G

6109372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673905-C-T

6109479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673972-T-A

6109479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673972-T-C

6109496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71673989-A-G

6109515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674002-T-C

6109564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674047-C-T

6109577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674058-T-C

6109876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674348-A-G

6109880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674352-G-A

http://identifiers.org/hco/17/GRCh38#6109999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71674427-A-C

6110514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71674908-G-A

6110515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71674909-A-G

http://identifiers.org/hco/17/GRCh38#6110619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71674992-A-C

6110626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71674999-G-T

6110734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71675062-G-T

6110803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 71675127-A-G

6110803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 71675127-A-T

6110951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71675280-A-G

http://identifiers.org/hco/17/GRCh38#6110957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71675286-C-A

6110957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71675286-C-G

6110957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71675286-C-T

6110973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71675307-C-T

6111004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71675338-G-C

6115985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

6115985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-C

6116733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71676791-A-G

6116904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71676948-C-T

6117230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677666-G-A

6117360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677817-C-G

6117360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677817-C-T

6117520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677950-G-A

6117564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677991-T-C

6117569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71677996-C-T

6117573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678000-G-A

6117773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678362-T-A

6117773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678362-T-C

http://identifiers.org/hco/17/GRCh38#6117840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71678430-C-A

6117840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678430-C-T

6118118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71678674-G-C

6118274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678782-A-G

http://identifiers.org/hco/17/GRCh38#6118302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71678807-C-A

6118302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71678807-C-T

6120508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71679694-G-A

http://identifiers.org/hco/17/GRCh38#6120521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71679707-C-A

6120521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71679707-C-G

6120521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 71679707-C-T

http://identifiers.org/hco/17/GRCh38#6120529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71679715-C-A

6120529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71679715-C-T

6120550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 71679736-G-A

6120705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71679889-C-T

http://identifiers.org/hco/17/GRCh38#6120759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71679940-C-A

6120759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71679940-C-T

http://identifiers.org/hco/17/GRCh38#6120845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71680027-A-C

6120867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680059-A-T

6120947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680142-G-C

6120947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680142-G-T

http://identifiers.org/hco/17/GRCh38#6121047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71680241-A-C

6121082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680264-G-A

6121082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680264-G-T

6121191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680367-G-A

6121191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680367-G-T

6121201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680379-G-A

6121201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680379-G-T

http://identifiers.org/hco/17/GRCh38#6121204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71680382-C-A

6121204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 71680382-C-T

6121501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680659-A-G

6121503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680661-C-T

6121512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680668-G-T

6121559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680703-G-T

6121581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680725-G-A

6121581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680725-G-C

6121581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680725-G-T

6121612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680757-T-C

6121614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680759-G-T

6121651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680792-G-A

6121657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680798-G-A

6121657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71680798-G-T

http://identifiers.org/hco/17/GRCh38#6121886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71681744-C-A

6121886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681744-C-T

http://identifiers.org/hco/17/GRCh38#6121913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71681750-C-A

6121913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681750-C-T

6121984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681759-G-A

6121984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681759-G-T

6122078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681834-G-A

6122078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681834-G-T

6122123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681876-G-T

6122129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681882-G-T

6122162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681913-T-C

6122166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681917-G-A

6122171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681919-T-C

http://identifiers.org/hco/17/GRCh38#6122200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71681948-C-A

6122200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71681948-C-G

6122255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71682004-T-C

6122436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684581-T-C

6122437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684582-T-C

6122447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684592-T-C

6122481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684624-C-T

6122527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684637-G-T

6122651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684801-G-A

6122651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684801-G-C

6122651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684801-G-T

6122669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684819-A-G

6122744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71684928-A-G

6122819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685019-G-A

6122946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685035-G-T

6122948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685037-G-A

6123055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685109-T-C

6123055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685109-T-G

6123117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685154-T-C

6123127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685159-G-A

http://identifiers.org/hco/17/GRCh38#6123138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71685170-C-A

http://identifiers.org/hco/17/GRCh38#6123212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71685250-C-A

6123212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685250-C-G

6123212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685250-C-T

http://identifiers.org/hco/17/GRCh38#6123588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71685623-A-C

6123683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685697-A-G

6123688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685703-T-G

6123775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685794-G-T

6123798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685817-G-T

6123932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685915-A-G

6123953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29060
most severe consequence: 3 prime UTR variant
orthologous variants: 71685933-C-T